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Volume 122, Issue 3, Pages 481-487 (September 2008)


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Advances in upper airway diseases and allergen immunotherapy in 2007

Carol Saltoun, MD, Pedro C. Avila, MDCorresponding Author Informationemail address

Received 15 April 2008; received in revised form 22 June 2008; accepted 24 June 2008. published online 11 August 2008.

The purpose of this review is to highlight important articles on upper airway diseases and immunotherapy that appeared in 2007. Advances in rhinitis include the realization that allergic rhinitis might be caused by local nasal IgE sensitization to aeroallergens in the absence of systemic evidence of IgE sensitization. After inhalation, allergens might reach systemic circulation. Epidemiologic studies continue to show that allergic rhinitis impairs school performance and is a risk factor for future asthma. New pathways are being identified in chronic sinusitis, as well as in different types of allergic ocular diseases. New treatments for patients with allergic rhinitis include use of β-1,3-glucan, a mushroom product that can reduce allergic symptoms by inducing TH1 response, and olopatadine nasal spray. Studies on immunotherapy in 2007 suggest that sublingual immunotherapy induces similar immunologic alterations as those induced by subcutaneous immunotherapy, although to a lesser degree. Among allergists in the United States, there is a sizable variation in clinical practice, particularly related to concomitant administration of immunotherapy and β-blockers, to administration of angiotensin-converting enzyme inhibitors, and to patients with HIV or autoimmune diseases. The combination of omalizumab with allergen subcutaneous immunotherapy can enhance clinical efficacy. Recombinant technology can modify allergen structure to prevent binding to IgE (allergenicity) while enhancing immunogenicity (stimulation of T cells), which might improve the safety and efficacy of immunotherapy.

Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Ill

Corresponding Author InformationReprint requests: Pedro C. Avila, MD, Northwestern University Feinberg School of Medicine, Division of Allergy-Immunology, 676 North Saint Clair St, Room 14-018, Chicago, IL 60611.

 Supported by an Ernest S. Bazley Grant to Northwestern University.

 Disclosure of potential conflict of interest: P. C. Avila has received honoraria from Key Pharmaceuticals for lectures given and has received grants from Genentech and the Asthma and Allergy Foundation of America. C. Saltoun has reported that she has no conflict of interest.

PII: S0091-6749(08)01176-7

doi:10.1016/j.jaci.2008.06.027


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