Abstract | OBJECTIVE: DESIGN: Quantitative reverse transcription-polymerase chain reaction (RT-PCR) analysis. SETTING: Academic research. PARTICIPANTS: Primary fibroblast lines were established from human nasal polyp biopsy tissue specimens (n = 5) removed at polypectomy. MAIN OUTCOME MEASURES: RESULTS: Combined stimulation with interleukin 4 (IL-4) and tumor necrosis factor alpha ( TNF-alpha) or with poly IC and IL-4 induced TARC production. Combined exposure of cells to poly IC, IL-4, and TNF-alpha resulted in substantial amounts of TARC release into the culture medium. Quantitative RT-PCR analysis revealed that simultaneous stimulation with those 3 compounds induced a tremendous increase in the amount of TARC mRNA in the nasal polyp fibroblasts. CONCLUSION:
Nasal polyp fibroblasts contribute to T(H)2 cell infiltration and RNA virus-induced exacerbation of T(H)2-type airway inflammatory conditions such as allergic chronic sinusitis.
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Authors | Manabu Nonaka, Nozomu Ogihara, Akira Fukumoto, Atsuko Sakanushi, Ruby Pawankar, Toshiaki Yagi |
Journal | Archives of otolaryngology--head & neck surgery
(Arch Otolaryngol Head Neck Surg)
Vol. 134
Issue 6
Pg. 630-5
(Jun 2008)
ISSN: 1538-361X [Electronic] United States |
PMID | 18559731
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Adjuvants, Immunologic
- CCL17 protein, human
- Chemokine CCL17
- Tumor Necrosis Factor-alpha
- Interleukin-4
- Poly I-C
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Topics |
- Adjuvants, Immunologic
(pharmacology)
- Cells, Cultured
- Chemokine CCL17
(biosynthesis)
- Fibroblasts
(drug effects, immunology)
- Humans
- Interleukin-4
(pharmacology)
- Nasal Polyps
(immunology)
- Poly I-C
(pharmacology)
- Tumor Necrosis Factor-alpha
(pharmacology)
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