4.7 Article

The effects of an anti-IL-13 mAb on cytokine levels and nasal symptoms following nasal allergen challenge

期刊

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
卷 128, 期 4, 页码 800-U490

出版社

MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2011.05.013

关键词

Allergic rhinitis; nasal allergen challenge; anti-IL-13; mAb

资金

  1. Novartis Pharmaceuticals
  2. Novartis
  3. GlaxoSmithKline
  4. AstraZeneca
  5. Boehringer Ingelheim
  6. TEVA
  7. Roche
  8. Medical Research Council [G1000758B, G1000758] Funding Source: researchfish
  9. National Institute for Health Research [NF-SI-0508-10212] Funding Source: researchfish

向作者/读者索取更多资源

Background: IL-13 is a key T(H)2 cytokine that is implicated in allergic responses. Objective: We evaluated the effects of an anti-IL-13-blocking antibody compared with placebo on repeated nasal allergen challenge responses in hay fever patients out of season. Methods: We performed a parallel group double-blind study of anti-IL-13 (single dose, 6 mg/kg intravenously, n = 16) and placebo (n = 15), with an additional open label group given a topical nasal corticosteroid (n = 5). Subjects received intranasal timothy grass pollen (Phleum pratense P5 allergen), and serial samples of nasal mucosal lining fluid were taken by using synthetic absorptive matrix and by nasal lavage. Results: Administration of anti-IL-13 on day 1 resulted in a significant decrease in IL-13 levels in synthetic absorptive matrix eluates compared with placebo (area under the curve 0-8 hours, change from baseline) during the late phase after nasal allergen challenge on day 5 (P < .05) and day 7 (P < .01). There were no apparent effects of anti-IL-13 treatment on nasal lavage eosinophil numbers or total nasal symptom scores versus placebo. However, in a subgroup with high late-phase IL-13 levels at screening, there was a trend for a decrease in total nasal symptom scores after nasal allergen challenge on day 5, when compared with subjects with low IL-13 levels (P < .10). Nasal fluticasone caused suppression of IL-13 (P < .05 on day 5) as well as IL-5 (P < .01 on day 5) levels in the late phase compared with placebo. Conclusions: Anti-IL-13 had specific pharmacodynamic action in this nasal allergen challenge model, causing profound inhibition of nasal lining fluid IL-13 responses. In addition, there was a possible effect of anti-IL-13 treatment on total nasal symptom scores in a subgroup with high late-phase nasal IL-13 levels at screening. (J Allergy Clin Immunol 2011;128:800-7.)

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