Volume 124, Issue 2 , Pages 185-192.e9, August 2009
Indoor allergens in school and day care environments
Article Outline
- Abstract
- Exposure to indoor allergens in day care and school environments
- Indoor allergen exposures in day care and school environments in relation to allergy and asthma
- Environmental control, remediation, and interventions in school environments
- Summary and conclusions
- Research needs and recommendations
- Acknowledgment
- Table E1.
- Table E2.
- Table E3.
- Table E4.
- Table E5.
- References
- References
- Copyright
Most studies that have examined exposure to indoor allergens have focused on home environments. However, allergen exposures can be encountered in environments other than the home. For example, many children spend a large part of their time in schools and day care facilities. Over the past 2 decades, a large number of studies have been conducted in school and day care environments. However, the role of indoor exposures in allergy and asthma development or morbidity in these settings is not well characterized. The purpose of this review is to evaluate the importance of indoor allergen exposures in school and day care settings. We summarize the key findings from recent scientific literature, describe exposure characteristics, discuss the role of these exposures in relation to asthma and allergy symptoms, and provide information on the effectiveness of published interventions.
Key words: Allergen, indoor, exposure, asthma, allergy, school, day care
Abbreviation used: MUP, Mouse urinary protein (mouse allergen)
Information for Category 1 CME Credit
Credit can now be obtained, free for a limited time, by reading the review articles in this issue. Please note the following instructions.
Method of Physician Participation in Learning Process: The core material for these activities can be read in this issue of the Journal or online at the JACI Web site: www.jacionline.org. The accompanying tests may only be submitted online at www.jacionline.org. Fax or other copies will not be accepted.
Date of Original Release: August 2009. Credit may be obtained for these courses until July 31, 2011.
Copyright Statement: Copyright © 2009-2011. All rights reserved.
Overall Purpose/Goal: To provide excellent reviews on key aspects of allergic disease to those who research, treat, or manage allergic disease.
Target Audience: Physicians and researchers within the field of allergic disease.
Accreditation/Provider Statements and Credit Designation: The American Academy of Allergy, Asthma & Immunology (AAAAI) is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians. The AAAAI designates these educational activities for a maximum of 1 AMA PRA Category 1 Credit™. Physicians should only claim credit commensurate with the extent of their participation in the activity.
List of Design Committee Members: Authors: Päivi M. Salo, PhD, Michelle L. Sever, MSPH, and Darryl C. Zeldin, MD
Activity Objectives
Recognition of Commercial Support: This CME activity is supported by an educational grant from Merck & Co., Inc.
Disclosure of Significant Relationships with Relevant Commercial
Companies/Organizations: The authors have declared that they have no conflict of interest.
AIR SAMPLING
There are multiple methods to sample aeroallergens, including sedimentation/gravity sampling (nonquantitative), rotating arm impactors, suction impactors, centrifugal sampling, and filtration sampling. The selection of the method/device depends on several factors, including the characteristics of the aeroallergen(s) (eg, particle size), sampling conditions and time, and analytical techniques used for quantification.
AMBIENT RELATIVE HUMIDITY
Relative humidity is calculated as the amount of moisture in the air divided by the maximum amount of moisture possible in the air at a specified temperature. Dust mites thrive in environment with temperatures of 70°F to 80°F and greater than 55% relative humidity.
β-1,3 GLUCAN AND ADJUVANT
β-1,3 Glucans are glucose polymers in the cell walls of plants and fungi. Exposure to elevated levels of this glucose polymer has been associated with increased atopy, increased conjunctival/respiratory symptoms, and decreased FEV1. In addition, β-1,3 glucans can act as adjuvants to increase antigen-specific IgE levels in animal models.
CROSS-SECTIONAL
A cross-sectional analysis examines relationships or associations at a single point in time (as opposed to a prospective cohort study, which looks at a sample population over time). In a cross-sectional study, disease prevalence can be determined, but due to the single time point, a causal relationship between a risk factor and disease cannot be established.
ELISA
An ELISA uses a color detection system to quantify the amount of a protein of interest (antibody or antigen). In a sandwich ELISA a capture antibody is coupled to a solid phase followed by incubation with a biologic fluid (eg, serum, dust extract) and detection of the antigen by a second antibody.
LARGE-SIZED PARTICLE
Only particles of 5 μm or less reach the lower airway. For example, intact pollen grains (15-75 μm) have the greatest effects on the upper airway and conjunctiva because of their size and subsequent trapping before reaching the lower airways.
LOW INCOME
The definition of a low-income family is one in which the income from the preceding year does not exceed 150% of the poverty line income. In 2009, the low-income threshold for the 48 contiguous states was defined as $33,075 for a family of 4 (poverty level of $22,050 for a family of 4).
TAPE SAMPLING
A hand-held roller with adhesive tape can be used to collect samples from clothing. Rolled tape samples are immunostained to detect allergen.
VOLATILE ORGANIC COMPOUNDS
Volitile organic compounds include a variety of organic chemicals that are emitted as gases from certain solids and liquids. Many household products, such as paints, cleaning supplies, pesticides, printers, glues, adhesives, and permanent markers are sources of volitile organic compounds in indoor environments. Volatile organic compounds can be up to 10 times more concentrated in indoor air compared with those in outdoor air.
The Editors wish to acknowledge Seema Aceves, MD, PhD, for preparing this glossary.
Exposure and sensitization to indoor allergens are important risk factors for asthma and allergic respiratory diseases.1 Although the role of indoor allergen exposure in the development of allergic sensitization and asthma remains subject to debate, there is strong evidence that indoor allergens play a key role in triggering and exacerbating allergy and asthma symptoms.2
Most studies of indoor allergens have targeted home environments because homes are often considered the primary sites of exposure. Over the past decades, the importance of nonresidential indoor environments has also been recognized.3 For example, in schools and day care facilities, allergen and other indoor exposures can affect children's health because children spend a large part of their childhood and adolescent years in these environments.
This review focuses on the importance of indoor allergen exposures in day care and school environments. The purpose of this article is to summarize key findings from the scientific literature and to identify future research needs. Studies for this review were searched by using the following databases: PubMed, Embase, Web of Science, Scopus, and Education Resources Information Center. Although inhalation of food allergens might induce allergic reactions in sensitive individuals, food allergens, which can constitute an important part of allergen exposures in day care and school settings, are beyond the scope of this review. Furthermore, the relevance of exposures other than aeroallergens (eg, environmental tobacco smoke, endotoxin, volatile organic compounds, and other irritants) will not be discussed, although these exposures might also affect indoor air quality and occupants' health status.
Exposure to indoor allergens in day care and school environments
Study designs and exposure assessment
Indoor allergen exposures in schools and day care centers have been an area of continuing research interest. Studies have been conducted worldwide,4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 but the research has been most active in the United States and Scandinavian countries.16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35 Although most studies have targeted school environments, the number of studies that have assessed allergen levels in day care centers has increased over the past decade.7, 9, 11, 15, 19, 22, 24, 28 To date, studies have mainly been cross-sectional in design. Some studies, however, have examined seasonal variation in allergen levels.16, 20
Cat (Fel d 1), dog (Can f 1), dust mite (Der f 1 and Der p 1), cockroach (Bla g 1 and Bla g 2), and mouse (Mus m 1 and mouse urinary protein [MUP]) allergens and molds have been the most frequently studied allergens. Although sampling and analytic procedures used in the studies vary considerably, allergen concentrations are usually quantified by using antibody-based ELISAs.36 However, methodological differences can contribute to the variability of the findings and complicate comparisons between studies. For example, differences in sampling equipments (eg, flow rate, vacuum power, and collection devices), sampling locations, and used metrics can make comparisons difficult.36 In general, correlations between different sampling methods have been poor.37 In most studies allergen levels have been assessed in settled dust samples collected from various indoor sites. Air sampling techniques have been primarily used for pet allergens (eg, Fel d 1), which are carried on aerodynamically smaller-sized particles and remain airborne for longer periods of time. Studies that have assessed allergen levels on the surface of clothing have also used tape sampling.38
Allergen levels and exposure characteristics
Table E1, Table E2, Table E3, Table E4, Table E5 in this article's Online Repository at www.jacionline.org summarize the main findings on cat, dog, dust mite, cockroach, and mouse allergen levels from published studies that have examined indoor allergen exposures in day care and school environments in the past 2 decades.
Exposure to cat and dog allergensNumerous studies have shown that animal allergens can be present in environments in which no animals reside.3, 4 In schools and day care centers, cat (Fel d 1) and dog (Can f 1) allergens are frequently detected, but the levels of exposure vary greatly. In general, these common aeroallergens are found at low levels (see Table E1, Table E2) in these settings. Nonetheless, although the magnitude of exposure tends to be low, studies have demonstrated that allergen levels in educational facilities can be higher than in homes where no pets are present.21, 29
Cat and dog allergen levels have generally been found in higher levels in carpeted and upholstered areas.4, 10, 18, 19, 23, 26 Levels in carpeting are often significantly lower than levels in upholstered seats.4, 27 It is not uncommon that allergen levels in these locations sometimes exceed thresholds that have been associated with allergic sensitization (1.0 μg/g for Fel d 1 and 2.0 μg/g for Can f 1) or asthma symptoms in sensitized individuals (8.0 μg/g for Fel d 1 and 10.0 μg/g for Can f 1).39, 40 The highest average concentrations have been found in US and Swedish schools; in samples collected from chairs and desks, geometric means reached as high as 11.3 μg/g for Fel d 1 and 15.0 μg/g for Can f 1.29
There is strong evidence that clothing is the primary transfer mechanism and source of pet allergens.10, 17, 41, 42 Among schoolchildren, allergen levels have been found to be significantly higher in dust collected from pet owners' clothing than from clothing of non–pet owners.10, 38, 41 Still, allergen levels can be dependent on clothing type and washing frequency.10, 42 A recent study has suggested that in addition to clothing, human hair might be a source for transfer and deposition of pet allergens among schoolchildren.43 Several studies worldwide have demonstrated that levels of cat and dog allergens in day cares and schools correlate with the number of children and staff who have either dogs or cats at home or have frequent contacts with these pets.10, 15, 17, 24, 26, 44, 45 Increased allergen levels have been detected in both dust and air samples. For example, concentrations of Fel d 1 and Can f 1 in settled dust were significantly lower in Swedish day care centers in which neither children nor staff owned pets compared with centers in which cat and dog ownership was common (median Fel d 1 levels, 0.64 vs 5.45 μg/g; median Can f 1 levels, 0.39 vs 2.51 μg/g).45 In another study there was a 5-fold difference in median levels of airborne Fel d 1 between classes with many (>25%) and few (<10%) cat owners.17
In summary, published data suggest that schools and day care centers can be important sites of exposure to cat and dog allergens, particularly for susceptible individuals (eg, sensitized children who do not have pets at home). However, not all studies link these environments to increased exposure levels. The number of pet owners at school or day care centers is one of the strongest predictors of increased cat and dog allergen levels in these settings.
Exposure to dust mite allergensStudies show that dust mite allergens (Der f 1 and Der p 1) are found in low levels in many schools and day care facilities (Table E3). Reported levels are often similar or slightly lower than in corresponding local homes.5, 7 Because ambient relative humidity is a key environmental factor that influences mite populations,46 dust mite allergen levels are strongly associated with humidity levels. To survive and thrive, dust mites require that the relative humidity of air is greater than 55% for a sufficient period of time because water vapor in air is their main source of water. Although mite levels tend to exhibit seasonal fluctuations that parallel those in ambient relative humidity, additional factors, including human activities and heating, ventilation, and air conditioning practices, can influence indoor air humidity levels.46, 47 In the studied facilities the highest average concentrations were detected in Brazil and in some humid regions in the United States (eg, Florida, Texas, Alabama, North Carolina, and Virginia).16, 22, 23, 29 In contrast, very low dust mite allergen levels have been found in colder and drier climates (eg, Scandinavia).6, 21, 24, 25, 26, 29 Levels of Der p 1 were often higher in more humid regions.16, 22, 34 Although concentrations of Der f 1 and Der p 1 tend to be correlated, they can reflect biologic and ecologic differences between the 2 mite species. Furthermore, the presence of other mite species can also influence concentrations of Der p 1 and Der f 1.12, 46
As in residential environments, dust mite allergen levels in day care centers and schools tend to be significantly higher in carpeted areas.7, 14, 15, 16, 18, 34 Although this is a consistent finding throughout all geographic regions, the highest levels are often detected in humid climates. For example, high average concentrations (geometric mean, 7.0 μg/g) in carpeting were reported in rural schools in North Carolina.23 Furthermore, study sites in which dust mite allergen concentrations exceeded a provisional threshold level representing increased risk of sensitization (>2 μg/g) were typically located in humid regions.48 In Florida, for example, dust mite allergen levels were greater than 2 μg/g in 40% of the studied day care centers,22 and in Texas Der p 1 concentrations exceeded the threshold in all types of schoolrooms, particularly in libraries (68%).16 However, none of the median or mean concentrations exceeded a threshold (>10 μg/g) that has been associated with asthma symptoms.49 In addition to carpeting, upholstered furnishings (eg, mattresses, pillows, seats, stuffed animals, and toys) can also be important reservoirs for dust mite allergens, particularly in day cares and elementary schools.7, 11, 16 Although dust mite allergens can be transferred passively between environments,42 it is not known whether the amounts of passively transferred allergen are clinically relevant.
Given that dust mite allergens are primarily associated with large-size particles that settle rapidly, few studies have examined airborne dust mite allergen levels in day care or school environments. A recent study demonstrated that airborne mite allergens were present in the majority of the studied day care centers (80%) in which group 1 mite allergen levels in dust exceeded the clinically relevant threshold (>2 μg/g).22 Airborne dust mite allergen levels were significantly lower during the nighttime, suggesting that mite allergens can become airborne because of reservoir disturbance during daily activities in day care settings. The highest airborne levels were recorded in the day care center with the highest mite allergen level in the carpet (21.8 μg/g).
In summary, dust mite allergen levels in schools and day care centers are associated with climatic, geographic, and building-related factors. Carpeting and upholstered furnishings are important reservoirs and sources of exposure in schools and day care centers, particularly in humid regions.
Exposure to cockroach and rodent allergensMost studies that have examined levels of cockroach (Bla g 1 and Bla g 2) and rodent (MUP) allergens in schools and day care centers have been conducted in the United States (Table E4, Table E5). Cockroach and mouse allergens are commonly detected in schools that serve low-income and inner-city populations, as well as in rural schools.16, 18, 20, 23, 28, 30, 31, 34, 35 A recent study found detectable levels of cockroach allergen in 71% of the dust samples.20 In another study mouse allergen was found in 100% of the samples.28 Cockroach and mouse allergens have also been present in airborne samples, although the detection frequency has been much lower than in dust samples (21% for Bla g 2 and 5% for MUP).20
Allergen levels show great variability between and within schools.18, 20, 35 For example, geometric mean concentrations for mouse allergen varied from 0.21 to 133 μg/g in a recent study.20 Although increased cockroach allergen levels (>2 U/g) have been found in many schools,16, 30, 31 low allergen levels are not uncommon in inner-cities.35 Increased cockroach allergen levels have also been reported in rural schools in the United States and some other countries.4, 11, 12, 23 However, all median or mean concentrations of cockroach allergen were lower than a threshold of 8 U/g, which has been associated with asthma exacerbation.50 Some studies have suggested that exposure to cockroach and mouse allergens in schools and day care centers might be similar to that which occurs in homes.20, 22, 31 On the other hand, a recent study demonstrated that exposure to mouse allergen can be significantly higher in schools than in homes.35
The highest levels of cockroach and mouse allergens are often found in cafeterias, kitchens, or rooms where food sources are present.18, 31, 35 In an inner-city school kitchen, cockroach allergen concentration was reported to be as high as 591 U/g31; correspondingly, the highest mouse allergen concentration was found in a school cafeteria (238 μg/g).35 Visual evidence of cockroach and rodent infestations in schools is another factor that is strongly associated with cockroach and mouse allergen levels.20, 31 Therefore indirect exposure to cockroach and rodent allergens in school environments is thought to be less likely.31, 35 It is important to note, however, that detectable levels of these allergens can be found without visual evidence of infestations.20 In contrast to pet and dust mite allergens, cockroach and mouse allergen levels have often been higher in noncarpeted areas.18, 20, 35 Nonetheless, high allergen levels have also been reported in carpeting in rural schools.23 It is unknown whether this reflects preferences in floor-covering choices in different locations; carpeting appears to be uncommon in inner-city schools.20, 35 Studies have shown that cockroach and mouse allergen levels can also vary by season and region.16, 20, 30
In summary, recent studies suggest that schools might be important sites for exposure to cockroach and mouse allergens, particularly in locations where roach and rodent infestations are common. However, information on the relative importance of cockroach and mouse allergen exposures in schools and day cares is limited.
Exposure to fungal allergensSeveral molds produce allergens that can be risk factors for allergic disease, including asthma.51 However, a major limitation in assessing exposure to fungal allergens has been the difficulty of the accurate quantification of the exposure. Exposure to fungal allergens has usually been estimated by using indirect methods, considering spores as indicators of the presence of allergens.51 Nonetheless, spore counts might not accurately reflect allergen exposure because allergen content in spores might vary and fungal allergens can be carried by means other than intact spores (eg, hyphal fragments).52 Because the availability of fungal immunoassays has been limited, only a few studies have assessed antigenic and allergenic components of fungi with immunoassays. One study that examined indoor allergen levels in day care facilities in the United States detected Alternaria alternata in 100% of dust samples,19 whereas in another study in Singapore, Asp f 1 was detected only in 15.4% of the samples.15
In summary, the complexity of the fungal exposure assessment and the lack of clearly defined threshold levels for fungi and substances derived from fungi (eg, allergens) have limited studies of fungal allergen exposures in day cares and school settings.
Indoor allergen exposures in day care and school environments in relation to allergy and asthma
Indoor air quality in schools and day care environments can affect millions of people, including students and staff. In the United States more than 50 million children are enrolled in public and private schools, and more than half of the children ages 3 to 5 years have attended center-based childcare programs over the past decade.53 Asthma and allergies are important public health concerns, not only in terms of health care costs but also in terms of lost productivity and reduced quality of life. For example, asthma and allergies account for more than 16 million missed school days per year in the United States.54, 55 Among school-aged children, asthma is the leading cause for absenteeism and can influence a child's academic performance and ability to participate in school-related activities.56 Importantly, the burden of asthma in schools extends beyond children; a recent report suggests that asthma within the educational services industry is an occupational health problem, particularly among teachers and teacher's aids.57
Although people tend to spend the majority of their time at home,58 allergen exposures can be encountered in environments other than the home. Schools and day care centers, where children and teachers spend a large part of their time, can be important sites for indoor allergen exposures. Especially for younger children, the timing of exposure can be critical because IgE-mediated sensitivity to specific aeroallergens develops in early childhood.59 In day care and elementary school classrooms, which often have a variety of potential allergen reservoirs (eg, upholstered furniture, pillows, stuffed animals, and toys), exposure levels might be higher than in middle and high school classrooms.16, 26 Moreover, the disturbance of allergen reservoirs is more likely because children at younger ages are more physically active.
Remarkably few studies to date have evaluated the relationship between asthma- and allergy-related outcomes and indoor allergen exposures in school and day care environments. Most studies that assessed allergen exposures in these environments were primarily designed to determine exposure characteristics. Although some studies reported prevalence rates for atopic outcomes, few studies used multivariate analysis to investigate relationships between health outcomes and exposures. Only a small number of the reviewed studies assessed allergen levels simultaneously in school and home environments (see Table E1, Table E2, Table E3, Table E4, Table E5).
In schools and day cares in which occupant density is high, the magnitude of indirect exposure to pet allergens might be sufficient to induce or maintain symptoms. Indeed, several Swedish studies have suggested that indirect exposure to cat and dog allergens in schools might influence asthma morbidity.25, 60, 61 In a recent study asthmatic children who had diagnosed cat allergy but did not report any direct contact with pets were evaluated after they returned to school after summer break. Those children who attended classrooms in which more than 18% of the students owned 1 or more cats reported significantly decreased peak expiratory flow rates, more asthma symptom days, and increased use of asthma medication than children who attended classes with fewer cat owners (≤18%).60
Another study demonstrated that asthmatic children with cat and dog sensitivity had significantly increased bronchial reactivity to inhaled methacholine after 1 school week.61 In this study concentrations of cat and dog allergens were found higher in school dust than in dust collected from children's homes, suggesting greater exposure in school than in home. Among Swedish schoolchildren, cat allergen levels in dust samples have also been associated with the incidence of asthma diagnosis.32
Recently, a German study examined whether exposure to cat allergen in the school environment was associated with allergic sensitization rates.62 Among school-aged children who did not have regular contact with cats, cat-specific sensitization rates increased in a dose-response fashion, depending on the percentages of students in class or school reporting regular contact with cats.
In the United States only 1 study has examined asthma prevalence in relation to the presence of common indoor allergens in the school environment. This study found a positive correlation between asthma prevalence rates and levels of cockroach allergen in schools.18
Over the past decades, numerous studies have reported positive associations between respiratory morbidity (eg, asthma) and exposure to fungi in indoor environments,63, 64 including schools and day care centers.65, 66, 67, 68 However, the underlying mechanisms for the observed health effects are not well characterized. Although fungal allergens can induce IgE-mediated hypersensitivity,69 exposure to fungi might also induce non–IgE-mediated inflammatory and immunologic processes; particulates derived from fungi not only contain allergens but also contain a variety of biologically active molecules (eg, β-1,3-glucans).3, 70 It has also been suggested that fungal exposure might promote adjuvant effects on allergic immune responses.71
In summary, although published studies demonstrate the importance of the school environment, the relationship between allergic respiratory diseases and indoor allergen exposures in schools and day cares is not well characterized. Although studies suggest that exposure to pet allergens in schools might influence asthma morbidity, studies provide limited information on whether exposures to indoor allergens in schools and day cares contribute to the development of allergic sensitization and asthma.
Environmental control, remediation, and interventions in school environments
Most studies designed to evaluate methods for reducing indoor allergen exposures in schools and day care facilities have been conducted in Sweden and have primarily focused on reducing cat and dog allergen exposures. Swedish researchers found that cat allergen levels were significantly reduced in classrooms that required the use of special school clothing compared with control classrooms.38 Intervention measures, however, were rigorous; children with and without pets changed clothes separately, school clothes were worn and laundered only at the school, staff changed their clothes before entering the classroom, a separate entrance was used for allergic children, and no other children were allowed in the area of the school where the special school clothing classrooms were located. The study also showed that similar reductions in cat allergen levels were achieved by implementing a pet ownership ban in which parents agreed not to keep furred pets or birds at home.
Another intervention study examined whether increased cleaning and reduction of potential reservoirs were efficient measures to reduce cat allergen levels in classrooms.72 In the intervention classrooms open shelves, upholstery, carpets, curtains, and plants were removed, and cleaning was increased. Children were asked to avoid contact with pets in the mornings before school. The intervention classrooms were compared with control classrooms and allergy-prevention classrooms that had been established before the start of the study. The allergy-prevention classrooms, which were located in a separate school building, had implemented extensive allergen avoidance measures for several years. No differences in cat allergen levels were found in the intervention classrooms before and after the intervention. The allergy-prevention classrooms had a trend toward lower levels of cat allergen than both the intervention and control classrooms.
An earlier Swedish study also evaluated whether extensive renovation, installation of a new ventilation system, ventilated floors, cleaning habits, and pet-avoidance measures (ie, families and personnel avoiding direct and indirect contacts with pets) influence cat and dog allergen levels.73 The intervention measures reduced cat and dog allergen levels substantially (6-fold reduction for Fel d 1 and 10-fold reduction for Can f 1) in a day care facility.
In Australia a “low-allergen” school was designed to reduce exposure to dust and hazardous chemicals.74 In the low-allergen school several measures were implemented. These included reducing potential dust reservoirs, improving ventilation, introducing materials with lower emissions of volatile organic compounds and dust particles, and using central vacuuming and radiant heating systems. Allergen concentrations and other environmental end points were measured in the low-allergen school and 3 other schools to evaluate the effectiveness of this intervention. The levels of dust mite and cat allergens tended to be lower in the low-allergen school, but differences between schools did not reach statistical significance.
One US study investigated the effectiveness of measures to reduce cockroach allergen levels.75 In an urban dormitory, which was chronically infested with cockroaches, successful abatement was accomplished by using routine extermination and vacuuming.
A number of interventions have been conducted to reduce exposure to molds and moisture in schools and day care facilities. Most of the studies have been conducted in Nordic countries.76, 77, 78, 79, 80 Renovations and repairs of moisture-damaged classrooms and buildings were found to be effective at reducing mold exposure in schools and day care facilities and were associated with improvement in building occupants' symptoms. Improvements in ventilation (eg, increased air-exchange rates) might also affect relative humidity and concentrations of airborne viable molds. In a recent study new ventilation systems improved indoor air quality and reduced asthma symptoms among students in intervened schools.81 In the United States a small pilot study that combined dehumidification with high-efficiency particulate air filtration reported reductions in airborne fungal spore counts.82 Because of the increased concern about indoor mold exposures in school and home environments, a variety of programs and guidelines have been launched over the past decades. For example, in the United States the US Environmental Protection Agency has provided guidance and tools for schools in addressing mold and remediation-related issues.83
In summary, multifaceted approaches might be needed to decrease indoor allergen levels in school and day care settings. Combined allergen-avoidance measures, such as improvements in ventilation systems, control of excess moisture, reductions in potential dust reservoirs, regular and thorough cleaning and maintenance, pest control, and use of special school clothing, might help to decrease exposure to indoor allergens in school and day care environments. However, there is limited information on how to choose and implement the most cost-effective intervention approach and the extent to which reductions in allergen exposures in these environments influence allergy- and asthma-related morbidity.
Summary and conclusions
We have summarized the key findings of the review in Table I. Exposure to indoor allergens in school and day care environments is common. However, published data show that levels of allergens are highly variable. Allergen levels can vary by time, location, and type of room within the building. This is not surprising because variety of physical (eg, humidity, temperature), structural (eg, age and type of building/room/surface), and behavioral (eg, pet ownership among children and staff, cleaning, and maintenance practices) factors can influence indoor allergen levels. The relative importance of different allergens can vary in different parts of the world depending on a variety of geographic, climatic, and cultural factors. Allergen levels in schools and day care facilities are often lower than levels that have been reported in homes. Nonetheless, it is not unusual that allergen levels in these settings exceed thresholds that have been associated with allergic sensitization and asthma morbidity. It has also been demonstrated that allergen levels in schools can be significantly higher than in the home environment. Carpeting, upholstered furnishings, and clothing are important reservoirs for allergens, particularly for pet and dust mite allergens. Because allergens are also transported passively to school and day care environments, exposure to allergens can occur either directly or indirectly. Schools and day care facilities might be important sources of allergen exposures, but there are limited data available to evaluate to what extent these exposures contribute to allergic sensitization and exacerbation of allergic symptoms. Information on cost-effective intervention strategies is also limited; in published studies the effectiveness of the interventions varied substantially.
Table I. Summary of the key findings
| Exposure to indoor allergens in day care and school environments |
| Indoor allergen exposures in relation to allergy and asthma |
| Environmental control, remediation, and interventions |
Research needs and recommendations
Over the past 2 decades, a considerable amount of research has been conducted on indoor allergen exposures in school and day-care environments. Although several guidelines have been developed and a variety of programs have been initiated to sustain asthma- and allergy-friendly schools in the United States and abroad,84, 85, 86 further research is warranted. Studies are needed to assess the extent to which school and day care environments contribute to allergic sensitization and asthma morbidity. Published data provide limited information on the potential additive effects of school or day care exposures in relation to allergy and asthma outcomes. For instance, few studies have collected information on health outcomes and exposure levels in schools/day cares and homes simultaneously; further studies addressing this issue are needed. Although schools and day care environments might not be primary sites for exposure, sensitization, or both to the dominant local allergen or allergens, it is essential to establish cost-effective approaches to reduce allergen levels in these indoor environments. Allergen exposures in school and day care settings might compromise the effectiveness of allergen avoidance measures used at home. From a public health perspective, it would be important to examine the extent to which various interventions are able to influence exposure levels and building occupants', children's, and staff members' allergy- and asthma-related morbidity. Economic analysis would help to evaluate the cost-effectiveness and clinical benefits of future interventions.
We thank Ms Stephenie Holmgren and Dr Larry Wright for their assistance with the literature search.
Table E1.
Studies assessing cat allergen (Fel d 1) levels in schools and day care facilities
| Country | Study design | Sampling methods and surface† | Allergen levels (μg/g unless otherwise noted) | Health outcomes assessed? | Reference |
|---|---|---|---|---|---|
| United States | Cross-sectional (spring and fall), 41 elementary schools in 3 cities | Dust, hard | Range of median levels for all sites: 0.02-0.4 | No | E16 |
| Dust, soft | |||||
| United States | Cross-sectional, 12 elementary schools | Dust, hard | Mean (range) for all samples: 1.66 (0.2-12) | Yes | E18 |
| Dust, soft | |||||
| United States | Cross-sectional, 89 day care centers | Dust, hard | Geometric mean (SE): 0.39 (0.21) | No | E19 |
| Dust, soft | Geometric mean (SE): 2.28 (1.45) | ||||
| United States | Cross-sectional, 20 day care centers | Dust | Mean (SE): 16.6-31.7 U/g | No | E22 |
| United States | Cross-sectional, 1 middle school (tiled) and 1 elementary school (carpeted) | Dust, tiled | Geometric mean (GSD): 4.8 (0.0035) | No | E23 |
| Dust, carpeted | Geometric mean (GSD): 6.0 (0.0017) | ||||
| Air, tiled | Geometric mean (GSD): 0.097 ng/m3 (0.0061 ng/m3) | ||||
| air-carpeted | Geometric mean (GSD): 0.064 ng/m3 (0.0054 ng/m3) | ||||
| United States | Cross-sectional, 33 preschools | Dust | Median (range): 0.4 (<0.02-4.3) | No | E28 |
| United States | Cross-sectional, 2 middle schools∗ | Dust | Geometric mean (range) floor: 0.9 (<0.2-2.4), 1.5 (1-4.4) Geometric mean (range) desk/chair: 11.3 (0.1-90), 4.8 (<0.4-185) Geometric mean (range) combined: 2.7 (<0.4-90), 2.3 (<0.4-185) | Yes | E29 |
| United States | Cross-sectional in winter, spring, and fall; 2 elementary schools | Dust, soft | Range: <0.015-4.67 | No | E30 |
| United States | Cross-sectional, 4 elementary schools∗ | Dust | Geometric mean: 0.56 | Yes | E35 |
| United States | Cross-sectional, 20 elementary schools | Dust, hard | Median (range): 0.031 (0.0048-0.28) | No | E34 |
| Dust, soft | Median (range): 0.091 (0.008-1.44) | ||||
| Brazil | Cross-sectional, 15 day cares, 15 preschools, 15 kindergartens, and 15 elementary schools | Dust | Range: undetectable–1.1 | No | E11 |
| China | Cross-sectional, 10 junior high schools | Dust | Median (range): <0.10 (<0.10-0.18) | Yes | E13 |
| France | Cross-sectional, 30 day care centers | Dust, hard | Range: <0.1-2.4 | No | E5 |
| Dust, soft | Range: <0.1-4.5, <0.1-4.1, <0.1-3.7 | ||||
| Korea | Cross-sectional, 12 schools | Dust, hard | Median (range): <0.2 (<0.2-1.4) | Yes | E8 |
| New Zealand | Cross-sectional, 18 day care centers and 18 kindergartens | Dust | Geometric mean (range): 1.24 (0.06-13.9) | No | E9 |
| New Zealand | Cross-sectional, 9 schools | Dust, clothes | Range of mean (95% CI): 1.49 (1.02-2.17)–13.17 (6.24-27.8) per garment | No | E10 |
| Dust, hard | Mean (95% CI): 0.33 (0.10-1.14) | ||||
| dust-soft | Mean (95% CI): 2.21 (1.28-3.84) | ||||
| Norway | Cross-sectional, 10 schools∗ | Dust, hard | Mean: 283 ng/m2 | No | E21 |
| Dust, soft | Mean: 3275 ng/m2 | ||||
| Norway | Cross-sectional, 81 schools, 24 day care centers | Dust, hard | Median: 0.2 | No | E24 |
| Dust, soft | Median: 1.5 (day care), 1.7 (school) | ||||
| Singapore | Cross-sectional, 10 schools and 10 day care centers∗ | Dust | Geometric mean (maximum) Childcare centers: 0.03 (0.2) Geometric mean (maximum) Schools: 0.03 (1.8) | No | E12 |
| Singapore | Cross-sectional, 104 day care centers | Dust | Geometric mean (range): 0.025 (0.01-0.41) | No | E15 |
| Sweden | Cross-sectional, 7 elementary schools (air) and 3 elementary classrooms (dust, clothes)∗ | Air | Median (IQR): 2.94 ng/m3 (2.37-4.77 ng/m3), 0.59 ng/m3 (0.45-0.81 ng/m3) | No | E17 |
| dust-clothes | Median (IQR): 3030 ng/garment (900-15,620 ng/garment), 146 ng/garment (86-234 ng/garment) | ||||
| Sweden | Cross-sectional, 8 schools | Dust, hard | Median (IQR): 0.86 (0.45-1.4) | Yes | E25 |
| Sweden | Cross-sectional, 7 day care centers | Dust | Median (range): 1.6 (<0.02-22.8) | No | E26 |
| Sweden | Cross-sectional, 4 schools | Dust | Geometric mean (range) chairs: 0.95 (0.63-1.63), Geometric mean (range) tables: 0.53 (0.03-1.58), Geometric mean (range) floors: 0.13 (<0.02-0.57) | No | E27 |
| Sweden | Cross-sectional, 22 elementary schools∗ | Dust | Geometric mean (range) floor: 0.3 (<0.2-8.8), Geometric mean (range) chair: 2.6 (<0.2-13), Geometric mean (range) combined: 0.8 (<0.1-13) | Yes | E29 |
| Sweden | Cross-sectional, 48 schools | Dust | Geometric mean (range): 0.11 (<0.015-0.39) | No | E32 |
| Sweden | Cross-sectional, 11 schools | Dust | Mean (range): 0.13 (<0.016-0.39) | Yes | E33 |
| United Kingdom | Cross-sectional, 5 schools∗ | Air | Only 1 of 9 samples detectable (0.79 ng/m3) | No | E4 |
∗Additional samples collected in homes. |
†Soft refers to carpeting, rugs and upholstered furniture, or other types of soft/porous sampling surfaces (eg, clothing). Hard generally refers to hard floors and other nonporous surfaces types (eg, tile, desks, and nonupholstered furniture). |
Table E2.
Studies assessing dog allergen (Can f 1) levels in schools and day care facilities
| Country | Study design | Sampling methods and surface† | Allergen levels (μg/g unless otherwise noted) | Health outcomes assessed? | Reference |
|---|---|---|---|---|---|
| United States | Cross-sectional, 12 elementary schools | Dust, hard | Mean (range) for all samples: 1.44 (0.1-9.6) | Yes | E18 |
| Dust, soft | |||||
| United States | Cross-sectional, 89 day care centers | Dust, hard | Geometric mean (SE): 0.29 (0.13) | No | E19 |
| Dust, soft | Geometric mean (SE): 2.13 (1.05) | ||||
| United States | Cross-sectional, 33 preschools | Dust | Median (range): 1.7 (0.1-33.6) | No | E28 |
| United States | Cross-sectional, 2 middle schools∗ | Dust | Geometric mean (range) floor: 1.2 (<0.5-4.8), 1.4 (<0.5-9.9) Geometric mean (range) desk/chair: 1.7 (0.6-7.9), 2.3 (<0.5-37) Geometric mean (range) combined: 1.4 (<0.5-7.9), 1.7 (<0.5-37) | Yes | E29 |
| United States | Cross-sectional, 4 elementary schools∗ | Dust | Geometric mean: 0.2 | Yes | E35 |
| Brazil | Cross-sectional, 15 day cares, 15 preschools, 15 kindergartens, and 15 elementary schools | Dust | Range: undetectable–3.3 | No | E11 |
| China | Cross-sectional, 10 junior high schools | Dust | Median (range): <0.20 (<0.20-0.53) | Yes | E13 |
| France | Cross-sectional, 30 day care centers | Dust, hard | Range: <0.2-1.2 | No | E5 |
| Dust, soft | Range: <0.2-4.5 | ||||
| Korea | Cross-sectional, 12 schools | Dust, hard | Median (range): 0.7 (<0.2-4.7) | Yes | E8 |
| New Zealand | Cross-sectional, 18 day care centers and 18 kindergartens | Dust | Geometric mean (range): 0.43 (0.01-4.09) | No | E9 |
| Norway | Cross-sectional, 81 schools, 24 day care centers | Dust, hard | Median: 1.7 | No | E24 |
| Dust, soft | Median: 10.0 (day care), 7.0 (school) | ||||
| Singapore | Cross-sectional, 10 schools and 10 day care centers∗ | Dust | Geometric mean (max) childcare centers: 0.1 (8.0) Geometric mean (max) schools: 0.1 (0.2) | No | E12 |
| Singapore | Cross-sectional, 104 day care centers | Dust | Geometric mean (range): 0.11 (0.04-2.86) | No | E15 |
| Sweden | Cross-sectional, 8 schools | Dust, hard | Median (IQR): 0.75 (0.44-3.0) | Yes | E25 |
| Sweden | Cross-sectional, 7 day care centers | Dust | Median (range): 4.3 (<0.06-21.0) | No | E26 |
| Sweden | Cross-sectional, 4 schools | dust | Geometric mean (range) chairs: 5.3 (1.7-28.2), Geometric mean (range) floors: 0.20 (0.06-0.51) | No | E27 |
| Sweden | Cross-sectional, 22 elementary schools∗ | Dust | Geometric mean (range) floor: 1.1 (<0.5-60), Geometric mean (range) hair: 15 (0.45-176), Geometric mean (range) combined: 3.3 (<0.5-176) | Yes | E29 |
| Sweden | Cross-sectional, 48 schools | Dust | Geometric mean (range): 0.38 (<0.10-3.99) | No | E32 |
| Sweden | Cross-sectional, 11 schools | Dust | Mean (range): 0.92 (<0.06-3.99) | Yes | E33 |
∗Additional samples collected in homes. |
†Soft refers to carpeting, rugs and upholstered furniture, or other types of soft/porous sampling surfaces (eg, clothing). Hard generally refers to hard floors and other nonporous surfaces types (eg, tile, desks, and nonupholstered furniture). |
Table E3.
Studies assessing dust mite allergen levels in schools and day care facilities
| Country | Study design | Sampling Methods and surface‖ | Allergen levels (μg/g unless otherwise noted) | Health outcomes assessed? | Reference |
|---|---|---|---|---|---|
| United States | Cross-sectional in spring and fall, 41 elementary schools in 3 cities | Dust, hard | Median range†: 0.01-2.8 Median range‡: 0.01-0.5 | No | E16 |
| Dust, soft | Median range†: 0.01-7.0 Median range‡: 0.01-1.3 | ||||
| United States | Cross-sectional, 12 elementary schools | Dust, hard | Mean (range) for all samples: 0.38 (0-11.9) | Yes | E18 |
| Dust, soft | |||||
| United States | Cross-sectional, 89 day care centers | Dust, hard | Geometric mean (SE)†: 0.02 (0.01) Geometric mean (SE)‡: 0.02 (0.01) | No | E19 |
| Dust, soft | Geometric mean (SE)†: 0.16 (0.08) Geometric mean (SE)‡: 0.04 (0.02) | ||||
| United States | Cross-sectional, 20 day care centers | Dust | Mean (SE)‡: 1.3 (0.9) | No | E22 |
| Mean (SE)†: 5.4 (6.9) | |||||
| Air | Mean(SE)†: 0.2 AU/m3 (0.6 AU/m3) | ||||
| United States | Cross-sectional, 1 middle school (tiled) and 1 elementary school (carpeted) | Dust, tiled | Geometric mean (GSD): 3.4 (0.0035) | No | E23 |
| Dust, carpeted | Geometric mean (GSD): 7.0 (0.0025) | ||||
| Air, tiled | Geometric mean (GSD): 0.074 ng/m3 (0.0044 ng/m3) | ||||
| Air, carpeted | Geometric mean (GSD): ≤0.032 ng/m3 (0.0023) ng/m3) | ||||
| United States | Cross-sectional, 33 preschools | Dust | Median (range)†‡: 0.6 (<0.02-22.0) | No | E28 |
| United States | Cross-sectional, 2 middle schools∗ | Dust | Yes | E29 | |
| United States | Cross-sectional in winter, spring, and fall; 2 elementary schools | Dust, soft | Range†‡: <0.01-0.12 | No | E30 |
| United States | Cross-sectional, 4 elementary schools∗ | Dust | Geometric mean†: 0.04 Geometric mean‡: 0.05 | Yes | E35 |
| United States | Cross-sectional, 20 elementary schools | Dust, hard | Median (range)†: 0.093 (0.007-18.3) Median (range)‡: 0.035 (0.007-0.13) | No | E34 |
| Dust, soft | Median (range)†: 0.580 (0.042-50.9) Median (range)‡: 0.057 (0.010-4.0) | ||||
| Brazil | Cross-sectional, 15 day care centers, 15 preschools, 15 kindergartens, and 15 elementary schools | Dust, hard | Geometric mean (range)†‡: 1.3 (<0.02-10.5), 1.9 (0.35-5.5), 0.07 (<0.02-0.25), 0.5 (0.06-4.7) | No | E11 |
| Dust, soft | Geometric mean (range)†‡: 2.6 (<0.02-16.2), 6.3 (1.3-30.7) | ||||
| China | Cross-sectional, 10 junior high schools | Dust | Only detected in 1 sample (0.32‡) | Yes | E13 |
| France | Cross-sectional, 30 day care centers | Dust, hard | Range†‡: <0.1-1.4 | No | E5 |
| Dust, soft | Range†‡: <0.1-5.3, <0.1-0.4, <0.1-2.3 | ||||
| Germany | Cross-sectional, 41 day care centers∗ | Dust | Median (IQR)†‡: 0.6 (0.2-1.5) | No | E7 |
| Korea | Cross-sectional, 12 schools | Dust, hard | Median (range): 0.25 (<0.2-0.9)‡, <0.2 (<0.2-0.3)† | Yes | E8 |
| Netherlands | Cross-sectional, 49 schools | Dust, hard | Geometric mean (range)†: 0.023 (<0.005-0.193) | No | E14 |
| Dust, soft | Geometric mean (range)†:0.044 (<0.005-18.7) | ||||
| New Zealand | Cross-sectional, 18 day care centers and 18 kindergartens | Dust | Geometric mean (range)†: 0.25 (0.01-103.8) | No | E9 |
| Norway | Cross-sectional, 10 schools∗ | Dust | Range‡: <1-5 ng/g | No | E21 |
| Dust, soft | Mean†: <3 ng/g | ||||
| Norway | Cross-sectional, 81 schools, 24 day care centers | Dust | Detected in 6 samples, maximum†: 0.2 | No | E24 |
| Singapore | Cross-sectional, 10 schools and 10 day care centers∗ | Dust | Geometric mean (maximum) childcare centers: 0.3 AU/g (2.7 AU/g)†, 0.2 AU/g (2.8 AU/g)‡, 564 AU/g (11,230 AU/g)§ Geometric mean (maximum) schools: 0.1 AU/g (3.7 AU/g)†, 0.2 AU/g (3.3 AU/g)‡, 632 AU/g (14,200 AU/g)§ | No | E12 |
| Singapore | Cross-sectional, 104 day care centers | Dust | Geometric mean (range): 0.05 (0.01-8.77)†, 0.21 (0.01-1.83)§ | No | E15 |
| Sweden | Cross-sectional, 8 schools | Dust, hard | None detected†‡ | Yes | E25 |
| Sweden | Cross-sectional, 7 day care centers | Dust | Median (range)†‡: <0.02 (<0.02-0.11) | No | E26 |
| Sweden | Cross-sectional, 22 elementary schools∗ | Dust | None detected†‡ | Yes | E29 |
| Sweden | Cross-sectional, 4 schools | Dust | No | E6 |
∗Additional samples collected in homes. |
†Der p 1 allergen measured. |
‡Der f 1 allergen measured. |
§Blo t 5 allergen measured. |
‖Soft refers to carpeting, rugs and upholstered furniture, or other types of soft/porous sampling surfaces (eg, clothing). Hard generally refers to hard floors and other nonporous surfaces types (eg, tile, desks, and nonupholstered furniture). |
Table E4.
Studies assessing cockroach allergen levels in schools and day care facilities
| Country | Study design | Sampling Methods and surface¶ | Allergen levels (μg/g unless otherwise noted) | Health outcomes assessed? | Reference |
|---|---|---|---|---|---|
| United States | Cross-sectional in spring and fall, 41 elementary schools in 3 cities | Dust, hard | All sites and classrooms had detectable levels‡ | No | E16 |
| Dust, soft | |||||
| United States | Cross-sectional, 12 elementary schools | Dust, hard | Mean (range) for all samples†‡: 1.49 (0-8) | Yes | E18 |
| Dust, soft | |||||
| United States | Cross-sectional, 89 day care centers | Dust, hard | Geometric mean (SE)†: 0.21 (0.07) | No | E19 |
| Dust, soft | Geometric mean (SE)†: 0.29 (0.10) | ||||
| United States | Cross-sectional in winter, spring and fall, 11 high schools∗ | Dust, hard | Range‡: <0.003-1.1 | No | E20 |
| Air | Range§: 0.058–3.8 | ||||
| United States | Cross-sectional, 20 day care centers | Dust | Mean (SE)‖: 0.26 (0.45) | No | E22 |
| United States | Cross-sectional, 33 preschools | Dust | Median (range)†: <0.4 U/g (<0.4-5.4 U/g) | No | E28 |
| Median (range)‡: <1.0 U/g (<1.0-1.4 U/g) | |||||
| United States | Cross-sectional, 2 middle schools∗ | Dust | Geometric mean (range) floor‡: <0.2, <0.2 | Yes | E29 |
| Geometric mean (range) desk/chair‡: <0.2, <0.2 | |||||
| Geometric mean (range) combined‡: <0.2, <0.2 | |||||
| United States | Cross-sectional in winter, spring, and fall; 2 elementary schools | Dust, soft | Range†: <0.01-12.3 | No | E30 |
| United States | Cross-sectional, 4 elementary schools | Dust, hard | Classrooms median (range)†: 2.4 (0-186) | No | E31 |
| All samples median (range)†: 2.6 (0-591) | |||||
| United States | Cross-sectional, 20 elementary schools | Dust, hard | Median (range)‡: 0.0052 (0.0015-0.140) | No | E34 |
| Dust, soft | Median (range)‡: 0.0057 (0.0016-0.015) | ||||
| United States | Cross-sectional, 1 middle school (tiled) and 1 elementary school (carpeted) | Dust, tiled | Geometric mean (GSD): 1.6 (0.0035) | No | E23 |
| Dust, carpeted | Geometric mean (GSD): 4.6 (0.0027) | ||||
| Air, tiled | Geometric mean (GSD): 0.049 μg/m3 (0.0030 μg/m3) | ||||
| Air, carpeted | Geometric mean (GSD): 0.087 μg/m3 (0.0042 μg/m3) | ||||
| United States | Cross-sectional, 4 elementary schools∗ | Dust | Geometric mean‡: 0.02 | Yes | E35 |
| Brazil | Cross-sectional, 15 day care centers, 15 preschools, 15 kindergartens, and 15 elementary schools | Dust, hard | Range of geometric mean† floor: 0.9-4.7 Range of geometric mean† chair/table: 3.6-5.2 | No | E11 |
| China | Cross-sectional, 10 junior high schools | Dust | None detected† | Yes | E13 |
| France | Cross-sectional, 30 day care centers | Dust, hard | Range: 2-14 U/mL†, 2-4 U/g‡ | No | E5 |
| Dust, soft | Range: <0.6-2 U/mL†, <0.6-6 U/g‡ | ||||
| Korea | Cross-sectional, 12 schools | Dust, hard | None detected† | Yes | E8 |
| New Zealand | Cross-sectional, 18 day care centers and 18 kindergartens | Dust | Geometric mean (range)‡: 0.028 (0.006-0.203) | No | E9 |
| Singapore | Cross-sectional, 10 schools and 10 day care centers∗ | Dust | Geometric mean (maximum) childcare centers†: 0.7 (15.1) Geometric mean (maximum) schools†: 5.9 (26.3) | No | E12 |
| Singapore | Cross-sectional, 104 day care centers | Dust | Geometric mean (range)†: 0.19 (0.02-5.21) | No | E15 |
| Sweden | Cross-sectional, 8 schools | Dust, hard | None detected† | Yes | E25 |
| Sweden | Cross-sectional, 22 elementary schools∗ | Dust | Geometric mean (range)‡ floor: 0.2 (<0.2-0.25), Geometric mean (range)‡c hair: 0.2 (<0.2-0.56), Geometric mean (range)‡ combined: 0.2 (<0.2-0.56) | Yes | E29 |
| United Kingdom | Cross-sectional, 5 schools∗ | Dust | Geometric mean (range)‡: 2.4 U/g (0.8-4.4 U/g) | No | E4 |
∗Additional samples collected in homes. |
†Bla g 1 allergen measured in units per gram unless otherwise noted. |
‡Bla g 2 allergen measured in micrograms per gram unless otherwise noted. |
§Bla g 2 allergen measured in nanograms per cubic meter. |
‖Per a 1 allergen measured in micrograms per gram unless otherwise noted. |
¶Soft refers to carpeting, rugs and upholstered furniture, or other types of soft/porous sampling surfaces (eg, clothing). Hard generally refers to hard floors and other nonporous surfaces types (eg, tile, desks, and nonupholstered furniture). |
Table E5.
Studies assessing mouse allergen levels in schools and day care facilities
| Country | Study design | Sampling Methods and surface‖ | Allergen levels (μg/g unless otherwise noted) | Health outcomes assessed? | Reference |
|---|---|---|---|---|---|
| United States | Cross-sectional, 12 elementary schools | Dust, hard | Mean (range) for all samples†: 1.44 (0.1-9.6) | Yes | E18 |
| Dust, soft | |||||
| United States | Cross-sectional, 89 day care centers | Dust, hard | Geometric mean (SE)†: 0.004 (0.002) | No | E19 |
| Dust, soft | Geometric mean (SE)†: 0.008 (0.004) | ||||
| United States | Cross-sectional in winter, spring, and fall; 11 high schools∗ | Dust, hard | Range‡: <0.2-1125 | No | E20 |
| Air | Range§: 0.09-0.25 | ||||
| United States | Cross-sectional, 33 preschools | Dust | Median (range)†: 0.18 (0.02-1.7) | No | E28 |
| United States | Cross-sectional, 4 elementary schools∗ | Dust | Geometric mean (range)‡: 1.66 (<0.25-238) | Yes | E35 |
| Singapore | Cross-sectional, 104 day care centers | Dust | Geometric mean (range): 0.007 (0.001-0.57) | No | E15 |
∗Additional samples collected in homes. |
†Mus m 1 allergen measured in micrograms per gram. |
‡MUP allergen measured in micrograms per gram. |
§Mus m 1 allergen measured in nanograms per cubic meter. |
‖Soft refers to carpeting, rugs and upholstered furniture, or other types of soft/porous sampling surfaces (eg, clothing). Hard generally refers to hard floors and other nonporous surfaces types (eg, tile, desks, and nonupholstered furniture). |
References
- . Indoor allergens and asthma: report of the Third International Workshop. J Allergy Clin Immunol. 1997;100(suppl):S2–S24
- . Exposure and sensitization to indoor allergens: association with lung function, bronchial reactivity, and exhaled nitric oxide measures in asthma. J Allergy Clin Immunol. 2003;112:362–368
- . Clearing the air: asthma and indoor exposures. Washington (DC): National Academy Press; 2000;
- Domestic allergens in public places. II: Dog (Can f1) and cockroach (Bla g 2) allergens in dust and mite, cat, dog and cockroach allergens in the air in public buildings. Clin Exp Allergy. 1996;26:1246–1252
- . Indoor allergen levels in day nurseries. J Allergy Clin Immunol. 1995;95:1158–1163
- . Allergens in school dust: II. Major mite (Der p I, Der f I) allergens in dust from Swedish schools. J Allergy Clin Immunol. 1995;95:1049–1053
- . House dust mite allergen levels in German day-care centers. Int J Hyg Environ Health. 2002;205:453–457
- . Respiratory symptoms, asthma and allergen levels in schools—comparison between Korea and Sweden. Indoor Air. 2007;17:122–129
- . Endotoxin and indoor allergen levels in kindergartens and daycare centres in Wellington, New Zealand. N Z Med J. 2007;120:U2400
- . Cat allergen (Fel d 1) levels on school children's clothing and in primary school classrooms in Wellington, New Zealand. J Allergy Clin Immunol. 1997;100:755–759
- . Daycare centers and schools as sources of exposure to mites, cockroach, and endotoxin in the city of Sao Paulo, Brazil. J Allergy Clin Immunol. 2002;110:582–588
- Prevalence and distribution of indoor allergens in Singapore. Clin Exp Allergy. 1997;27:876–885
- . A comparative study of asthma, pollen, cat and dog allergy among pupils and allergen levels in schools in Taiyuan city, China, and Uppsala, Sweden. Indoor Air. 2006;16:404–413
- . House dust mite allergen levels in dust from schools with smooth and carpeted classroom floors. Clin Exp Allergy. 1995;25:549–553
- . Determinants of indoor allergens in tropical child care centers. Pediatr Allergy Immunol. 2008;19:746–755
- Allergens in school settings: results of environmental assessments in 3 city school systems. J Sch Health. 2006;76:246–249
- . School as a risk environment for children allergic to cats and a site for transfer of cat allergen to homes. J Allergy Clin Immunol. 1999;103:1012–1017
- Environmental allergens and asthma in urban elementary schools. Ann Allergy Asthma Immunol. 2003;90:34–40
- . Exposure to indoor allergens in day-care facilities: results from 2 North Carolina counties. J Allergy Clin Immunol. 2005;116:133–139
- . Mouse and cockroach allergens in the dust and air in northeastern United States inner-city public high schools. Indoor Air. 2005;15:228–234
- . Dust from carpeted and smooth floors. VI. Allergens in homes compared with those in schools in Norway. Allergy. 1994;49:210–216
- . House dust mite, cat, and cockroach allergen concentrations in daycare centers in Tampa, Florida. Ann Allergy Asthma Immunol. 2001;87:196–200
- . Comparison of biocontaminant levels associated with hard vs. carpet floors in nonproblem schools: results of a year long study. J Expo Anal Environ Epidemiol. 2004;14(suppl 1):S41–S48
- . Allergens and endotoxin in settled dust from day-care centers and schools in Oslo, Norway. Indoor Air. 2005;15:356–362
- . Current asthma and respiratory symptoms among pupils in relation to dietary factors and allergens in the school environment. Indoor Air. 2005;15:170–182
- . Mite (Der p I, Der f I), cat (Fel d I) and dog (Can f I) allergens in dust from Swedish day-care centres. Clin Exp Allergy. 1995;25:119–126
- . Allergens in school dust. I. The amount of the major cat (Fel d I) and dog (Can f I) allergens in dust from Swedish schools is high enough to probably cause perennial symptoms in most children with asthma who are sensitized to cat and dog. J Allergy Clin Immunol. 1993;91:1067–1074
- Classroom aeroallergen exposure in Arkansas head start centers. Ann Allergy Asthma Immunol. 2008;100:358–363
- . Relevance of allergens from cats and dogs to asthma in the northernmost province of Sweden: schools as a major site of exposure. J Allergy Clin Immunol. 1999;103:1018–1024
- Indoor air quality in two urban elementary schools–measurements of airborne fungi, carpet allergens, CO2, temperature, and relative humidity. J Occup Environ Hyg. 2005;2:553–566
- . Cockroach allergen (Bla g 1) in school dust. J Allergy Clin Immunol. 1997;99:486–492
- . Incidence of asthma diagnosis and self-reported allergy in relation to the school environment—a four-year follow-up study in schoolchildren. Int J Tuberc Lung Dis. 2001;5:1059–1066
- . Asthma among secondary schoolchildren in relation to the school environment. Clin Exp Allergy. 1997;27:1270–1278
- Environmental allergens and irritants in schools: a focus on asthma. J Sch Health. 2002;72:33–38
- Mouse allergens in urban elementary schools and homes of children with asthma. Ann Allergy Asthma Immunol. 2009;102:125–130
- . Indoor allergens in settled school dust: a review of findings and significant factors. Clin Exp Allergy. 2005;35:126–136
- . Comparison of four allergen-sampling methods in conventional and allergy prevention classrooms. Clin Exp Allergy. 2002;32:1776–1781
- . Airborne cat allergen reduction in classrooms that use special school clothing or ban pet ownership. J Allergy Clin Immunol. 2004;113:1172–1177
- Domestic allergens in public places III: house dust mite, cat, dog and cockroach allergens in British hospitals. Clin Exp Allergy. 1998;28:53–59
- . Quantitative assessment of exposure to dog (Can f 1) and cat (Fel d 1) allergens: relation to sensitization and asthma among children living in Los Alamos, New Mexico. J Allergy Clin Immunol. 1995;96:449–456
- . Concentrations of cat (Fel d1), dog (Can f1) and mite (Der f1 and Der p1) allergens in the clothing and school environment of Swedish schoolchildren with and without pets at home. Pediatr Allergy Immunol. 1998;9:25–30
- . Exposure to mite and cat allergens on a range of clothing items at home and the transfer of cat allergen in the workplace. J Allergy Clin Immunol. 2000;106:874–879
- . Human hair is a potential source of cat allergen contamination of ambient air. Allergy. 2005;60:961–964
- . Indoor molds, bacteria, microbial volatile organic compounds and plasticizers in schools—associations with asthma and respiratory symptoms in pupils. Indoor Air. 2007;17:153–163
- Fel d 1 and Can f 1 in settled dust and airborne Fel d 1 in allergen avoidance day-care centres for atopic children in relation to number of pet-owners, ventilation and general cleaning. Clin Exp Allergy. 1999;29:626–632
- . Dust mite allergens: ecology and distribution. Curr Allergy Asthma Rep. 2002;2:401–411
- The house-dust mite: its biology and role in allergy. Proceedings of an international scientific workshop. Oslo, Norway, 4-7 September 1997. Allergy. 1998;53:1–135
- . Exposure to house-dust mite allergen (Der p I) and the development of asthma in childhood. A prospective study. N Engl J Med. 1990;323:502–507
- Dust mite allergens and asthma—a worldwide problem. J Allergy Clin Immunol. 1989;83:416–427
- The role of cockroach allergy and exposure to cockroach allergen in causing morbidity among inner-city children with asthma. N Engl J Med. 1997;336:1356–1363
- . Outdoor allergens. Environ Health Perspect. 2000;108(suppl 4):653–659
- . Allergen detection from 11 fungal species before and after germination. J Allergy Clin Immunol. 2003;111:285–289
- The condition of education. Jessup (MD): National Center for Education Statistics (NCES); 2007;Available at: http://nces.ed.gov/pubs2007/2007064_1.pdfAccessed February 14, 2009
- . Surveillance for asthma—United States, 1980-1999. MMWR Surveill Summ. 2002;51:1–13
- . The burden of allergic rhinitis. Allergy Asthma Proc. 2007;28:3–9
- . Asthma status and severity affects missed school days. J Sch Health. 2006;76:18–24
- Work-related asthma in the educational services industry: California, Massachusetts, Michigan, and New Jersey, 1993-2000. Am J Ind Med. 2008;51:47–59
- . It's about time: a comparison of Canadian and American time-activity patterns. J Expo Anal Environ Epidemiol. 2002;12:427–432
- Atopic characteristics of children with recurrent wheezing at high risk for the development of childhood asthma. J Allergy Clin Immunol. 2004;114:1282–1287
- Worsening of asthma in children allergic to cats, after indirect exposure to cat at school. Am J Respir Crit Care Med. 2001;163:694–698
- Markers of inflammation and bronchial reactivity in children with asthma, exposed to animal dander in school dust. Pediatr Allergy Immunol. 1999;10:45–52
- . Allergic sensitization owing to “second-hand” cat exposure in schools. Allergy. 2002;57:357–361
- . Effects of damp and mould in the home on respiratory health: a review of the literature. Allergy. 1998;53:120–128
- . Health risk assessment of fungi in home environments. Ann Allergy Asthma Immunol. 1997;78:544–556
- . Indoor air quality, ventilation and health symptoms in schools: an analysis of existing information. Indoor Air. 2003;13:53–64
- An approach to management of critical indoor air problems in school buildings. Environ Health Perspect. 1999;107(suppl 3):509–514
- Indoor air microbes and respiratory symptoms of children in moisture damaged and reference schools. Indoor Air. 2002;12:175–183
- . Fungal contamination of elementary schools: a new environmental hazard. Ann Allergy Asthma Immunol. 2003;90:203–208
- Prevalence of allergic sensitization to indoor fungi in West Virginia. Allergy Asthma Proc. 2008;29:29–34
- . Health effects of indoor fungi. Ann Allergy Asthma Immunol. 2005;94:313–32290
- . Mould extracts increase the allergic response to ovalbumin in mice. Clin Exp Allergy. 2004;34:1634–1641
- . Allergen avoidance does not alter airborne cat allergen levels in classrooms. Allergy. 2004;59:661–667
- . Allergen avoidance in a day-care center. Allergy. 1996;51:36–41
- . Indoor environmental quality in a “low allergen” school and three standard primary schools in Western Australia. Indoor Air. 2006;16:74–80
- . Short-term effects of extermination and cleaning on cockroach allergen Bla g 2 in settled dust. Ann Allergy Asthma Immunol. 1996;76:257–260
- Effects of moisture damage and renovation on microbial conditions and pupils' health in two schools—a longitudinal analysis of five years. J Environ Monit. 2007;9:225–233
- . Effects of moisture-damage repairs on microbial exposure and symptoms in schoolchildren. Indoor Air. 2005;15(suppl 10):40–47
- The remediation of mold damaged school—a three-year follow-up study on teachers' health. Cent Eur J Public Health. 2004;12:36–42
- . Airborne (1→3)-beta-D-glucan and airway disease in a day-care center before and after renovation. Arch Environ Health. 1997;52:281–285
- . Respiratory morbidity among children following renovation of a water-damaged school. Arch Environ Health. 2000;55:405–410
- . New ventilation systems at select schools in Sweden—effects on asthma and exposure. Arch Environ Health. 2000;55:18–25
- . A pilot study to investigate the effects of combined dehumidification and HEPA filtration on dew point and airborne mold spore counts in day care centers. Indoor Air. 2005;15:402–407
- . Mold remediation in schools and commercial buildings. Washington (DC): Environmental Protection Agency; 2001;EPA publication no. 402-K-01-001
- IAQ tools for schools: managing asthma in the school environment. Available at: http://www.epa.gov/iaq. Accessed February 16, 2009.
- Asthma and allergies at school—a Swedish national position paper. Allergy. 2002;57:454–457
- . Introduction: learning from each other about managing asthma in schools. J Sch Health. 2006;76:202–204
References
- . Indoor allergens and asthma: report of the Third International Workshop. J Allergy Clin Immunol. 1997;100(suppl):S2–S24
- . Exposure and sensitization to indoor allergens: association with lung function, bronchial reactivity, and exhaled nitric oxide measures in asthma. J Allergy Clin Immunol. 2003;112:362–368
- . Clearing the air: asthma and indoor exposures. Washington (DC): National Academy Press; 2000;
- Domestic allergens in public places. II: Dog (Can f1) and cockroach (Bla g 2) allergens in dust and mite, cat, dog and cockroach allergens in the air in public buildings. Clin Exp Allergy. 1996;26:1246–1252
- . Indoor allergen levels in day nurseries. J Allergy Clin Immunol. 1995;95:1158–1163
- . Allergens in school dust: II. Major mite (Der p I, Der f I) allergens in dust from Swedish schools. J Allergy Clin Immunol. 1995;95:1049–1053
- . House dust mite allergen levels in German day-care centers. Int J Hyg Environ Health. 2002;205:453–457
- . Respiratory symptoms, asthma and allergen levels in schools—comparison between Korea and Sweden. Indoor Air. 2007;17:122–129
- . Endotoxin and indoor allergen levels in kindergartens and daycare centres in Wellington, New Zealand. N Z Med J. 2007;120:U2400
- . Cat allergen (Fel d 1) levels on school children's clothing and in primary school classrooms in Wellington, New Zealand. J Allergy Clin Immunol. 1997;100:755–759
- . Daycare centers and schools as sources of exposure to mites, cockroach, and endotoxin in the city of Sao Paulo, Brazil. J Allergy Clin Immunol. 2002;110:582–588
- Prevalence and distribution of indoor allergens in Singapore. Clin Exp Allergy. 1997;27:876–885
- . A comparative study of asthma, pollen, cat and dog allergy among pupils and allergen levels in schools in Taiyuan city, China, and Uppsala, Sweden. Indoor Air. 2006;16:404–413
- . House dust mite allergen levels in dust from schools with smooth and carpeted classroom floors. Clin Exp Allergy. 1995;25:549–553
- . Determinants of indoor allergens in tropical child care centers. Pediatr Allergy Immunol. 2008;19:746–755
- Allergens in school settings: results of environmental assessments in 3 city school systems. J Sch Health. 2006;76:246–249
- . School as a risk environment for children allergic to cats and a site for transfer of cat allergen to homes. J Allergy Clin Immunol. 1999;103:1012–1017
- Environmental allergens and asthma in urban elementary schools. Ann Allergy Asthma Immunol. 2003;90:34–40
- . Exposure to indoor allergens in day-care facilities: results from 2 North Carolina counties. J Allergy Clin Immunol. 2005;116:133–139
- . Mouse and cockroach allergens in the dust and air in northeastern United States inner-city public high schools. Indoor Air. 2005;15:228–234
- . Dust from carpeted and smooth floors. VI. Allergens in homes compared with those in schools in Norway. Allergy. 1994;49:210–216
- . House dust mite, cat, and cockroach allergen concentrations in daycare centers in Tampa, Florida. Ann Allergy Asthma Immunol. 2001;87:196–200
- . Comparison of biocontaminant levels associated with hard vs. carpet floors in nonproblem schools: results of a year long study. J Expo Anal Environ Epidemiol. 2004;14(suppl 1):S41–S48
- . Allergens and endotoxin in settled dust from day-care centers and schools in Oslo, Norway. Indoor Air. 2005;15:356–362
- . Current asthma and respiratory symptoms among pupils in relation to dietary factors and allergens in the school environment. Indoor Air. 2005;15:170–182
- . Mite (Der p I, Der f I), cat (Fel d I) and dog (Can f I) allergens in dust from Swedish day-care centres. Clin Exp Allergy. 1995;25:119–126
- . Allergens in school dust. I. The amount of the major cat (Fel d I) and dog (Can f I) allergens in dust from Swedish schools is high enough to probably cause perennial symptoms in most children with asthma who are sensitized to cat and dog. J Allergy Clin Immunol. 1993;91:1067–1074
- Classroom aeroallergen exposure in Arkansas head start centers. Ann Allergy Asthma Immunol. 2008;100:358–363
- . Relevance of allergens from cats and dogs to asthma in the northernmost province of Sweden: schools as a major site of exposure. J Allergy Clin Immunol. 1999;103:1018–1024
- Indoor air quality in two urban elementary schools–measurements of airborne fungi, carpet allergens, CO2, temperature, and relative humidity. J Occup Environ Hyg. 2005;2:553–566
- . Cockroach allergen (Bla g 1) in school dust. J Allergy Clin Immunol. 1997;99:486–492
- . Incidence of asthma diagnosis and self-reported allergy in relation to the school environment—a four-year follow-up study in schoolchildren. Int J Tuberc Lung Dis. 2001;5:1059–1066
- . Asthma among secondary schoolchildren in relation to the school environment. Clin Exp Allergy. 1997;27:1270–1278
- Environmental allergens and irritants in schools: a focus on asthma. J Sch Health. 2002;72:33–38
- Mouse allergens in urban elementary schools and homes of children with asthma. Ann Allergy Asthma Immunol. 2009;102:125–130
(Supported by an educational grant from Merck & Co., Inc.)
Series editors: Joshua A. Boyce, MD, Fred Finkelman, MD, William T. Shearer, MD, PhD, and Donata Vercelli, MD
Supported by the Intramural Research Program of the National Institutes of Health, National Institute of Environmental Health Sciences (Z01 ES025041).
Terms in boldface and italics are defined in the glossary on page 186.
PII: S0091-6749(09)00803-3
doi:10.1016/j.jaci.2009.05.012
© 2009 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
Volume 124, Issue 2 , Pages 185-192.e9, August 2009
