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The Journal of Allergy and Clinical Immunology
Volume 122, Issue 6
, Pages
1145-1153.e3
, December 2008
Cigarette smoke combined with Toll-like receptor 3 signaling triggers exaggerated epithelial regulated upon activation, normal T-cell expressed and secreted/CCL5 expression in chronic rhinosinusitis
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Baseline gene expression in PNECs from HCs and subjects with CRS. Symbols (HC, open symbols; CRS, solid symbols) indicate level of expression relative to the housekeeping gene GAPDH. Subjects with CRS
Baseline gene expression in PNECs from HCs and subjects with CRS. Symbols (HC, open symbols; CRS, solid symbols) indicate level of expression relative to the housekeeping gene GAPDH. Subjects with CRS showed increased expression of TNF-α (4-fold increase; P = .02) and GRO-α (16-fold increase; P = .004) relative to HCs.
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Representative epithelial immunostaining for TNF-α, GRO-α, and RANTES in HCs and subjects with CRS. A, Subject with CRS showing predominantly epithelial staining for TNF-α. B, Subject with CRS showingRepresentative epithelial immunostaining for TNF-α, GRO-α, and RANTES in HCs and subjects with CRS. A, Subject with CRS showing predominantly epithelial staining for TNF-α. B, Subject with CRS showing epithelial and glandular immunostaining for GRO-α. C, Subject with CRS showing epithelial immunostaining for RANTES. Inserts in A and C show the same tissues immunostained with the secondary antibody alone. Similar patterns of immunostaining were found in HCs. Magnification ×200.
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Intensity of PNEC immunostaining in HCs versus subjects with CRS (N = 9 per group) for TNF-α (A), GRO-α (B), and RANTES (C). No statistically significant differences in immunostaining were found in HCIntensity of PNEC immunostaining in HCs versus subjects with CRS (N = 9 per group) for TNF-α (A), GRO-α (B), and RANTES (C). No statistically significant differences in immunostaining were found in HCs versus subjects with CRS.
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Inflammatory gene induction in HCs and subjects with CRS by CSE, TNF-α, LTA, LPS, CSE+TNF-α, CSE+LTA, and CSE+LPS. The ordinate shows fold increase in gene expression relative to GAPDH housekeeping geInflammatory gene induction in HCs and subjects with CRS by CSE, TNF-α, LTA, LPS, CSE+TNF-α, CSE+LTA, and CSE+LPS. The ordinate shows fold increase in gene expression relative to GAPDH housekeeping gene. No statistically significant differences were found between HCs and subjects with CRS except increased GRO-α, which patterned the increased baseline GRO-α in subjects with CRS.
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Inflammatory gene induction in HCs and subjects with CRS by CSE, dsRNA, and CSE+dsRNA. The ordinate shows fold increase in gene expression relative to GAPDH housekeeping gene. Statistically significanInflammatory gene induction in HCs and subjects with CRS by CSE, dsRNA, and CSE+dsRNA. The ordinate shows fold increase in gene expression relative to GAPDH housekeeping gene. Statistically significant differences between HCs and subjects with CRS were confined to greater induction of HBD2 and RANTES by CSE+dsRNA, as shown.
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Induction of IFN-β, IFN-λ1, IFN-λ2/3, TLR-3, and IL-17R by CSE, dsRNA, and CSE+dsRNA in HCs and subjects with CRS. The ordinate shows fold increase in gene expression relative to GAPDH housekeeping geInduction of IFN-β, IFN-λ1, IFN-λ2/3, TLR-3, and IL-17R by CSE, dsRNA, and CSE+dsRNA in HCs and subjects with CRS. The ordinate shows fold increase in gene expression relative to GAPDH housekeeping gene. CSE alone suppressed induction of IFN-β in subjects with CRS; however, CSE+dsRNA induced equivalent expression of IFN-β and the other gene studied.
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Viability of primary nasal epithelial cells after 1-hour pulse exposure to CSE assessed at 6 hours and 24 hours by Trypan blue dye exclusion. Viability after exposure to 5% CSE was 81% at 24 hours inViability of primary nasal epithelial cells after 1-hour pulse exposure to CSE assessed at 6 hours and 24 hours by Trypan blue dye exclusion. Viability after exposure to 5% CSE was 81% at 24 hours in both normal controls and patients with CRS.
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RANTES protein levels and correlation with RANTES mRNA expression in new set of PNEC culture supernatants. A, RANTES protein in PNEC culture supernatant measured by ELISA in 3 healthy controls and 3 sRANTES protein levels and correlation with RANTES mRNA expression in new set of PNEC culture supernatants. A, RANTES protein in PNEC culture supernatant measured by ELISA in 3 healthy controls and 3 subjects with CRS. B, Dot-plot of RANTES protein in PNEC culture supernatant versus RANTES mRNA relative expression in the same PNEC cultures (N = 8). Con, Control, unstimulated condition.
Supported by a grant from the Flight Attendants Medical Research Institute.
Disclosure of potential conflict of interest: D. L. Hamilos has received honoraria from Merck, Critical Therapeutics, Genentech, and Novartis; has consulting arrangements with GlaxoSmithKline, Novartis, Accentia, Schering-Plough, and Sinexus; has received research support from the Flight Attendants Medical Research Institute and Merck; and has received gifts from the GG Monks Foundation to purchase equipment. E. H. Holbrook has received research support from the National Institutes of Health-National Institutes of Deafness and Other Communication Disorders. S. T. Gray has served as a member of the American Academy of Otolaryngology and the American Rhinologic Society. N. Busaba is on the speakers' bureau for Sanofi-Aventis and Schering-Plough. The rest of the authors have declared that they have no conflict of interest.
PII: S0091-6749(08)01728-4
doi: 10.1016/j.jaci.2008.09.033
© 2008 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
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The Journal of Allergy and Clinical Immunology
Volume 122, Issue 6
, Pages
1145-1153.e3
, December 2008
