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Published ahead of print on October 5, 2006, doi:10.1165/rcmb.2006-0244OC
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American Journal of Respiratory Cell and Molecular Biology. Vol. 36, pp. 368-376, 2007
© 2007 American Thoracic Society
DOI: 10.1165/rcmb.2006-0244OC

Efficacy of IL-13 Neutralization in a Sheep Model of Experimental Asthma

Marion T. Kasaian, Debra D. Donaldson*, Lioudmila Tchistiakova, Kimberly Marquette, Xiang-Yang Tan, Ashfaq Ahmed, Bruce A. Jacobson, Angela Widom, Timothy A. Cook, Xin Xu, Anthony B. Barry, Samuel J. Goldman and William M. Abraham

Department of Inflammation, Wyeth Research, Cambridge, Massachusetts; and Department of Research, Mount Sinai Medical Center, Miami Beach, Florida

Correspondence and requests for reprints should be addressed to Marion T. Kasaian, Department of Inflammation, Wyeth Research, 200 CambridgePark Drive, Cambridge, MA 02140. E-mail: mkasaian{at}wyeth.com

IL-13 contributes to airway hyperresponsiveness, mucus secretion, inflammation, and fibrosis, suggesting that it plays a central role in asthma pathogenesis. Neutralization of IL-13 with sIL-13R{alpha}2-Fc (sIL-13R) reduces allergen-induced airway responses in rodent models of respiratory disease, but its efficacy in a large animal model has not been previously reported. In this study, we determined whether two different strategies for IL-13 neutralization modified experimental asthma in sheep. Sheep with natural airway hypersensitivity to Ascaris suum antigen were treated intravenously either with sIL-13R, a strong antagonist of sheep IL-13 bioactivity in vitro, or with IMA-638 (IgG1, {kappa}), a humanized antibody to human IL-13. Higher doses of IMA-638 were used because, although it is a potent antagonist of human IL-13, this antibody has 20 to 30 times lower binding and neutralization activity against sheep IL-13. Control animals received human IgG of irrelevant specificity. Sheep were treated 24 h before inhalation challenge with nebulized A. suum. The effects on antigen-induced early and late bronchial responses, and antigen-induced hyperresponsiveness, were assessed. Both sIL-13R and IMA-638 provided dose-dependent inhibition of the antigen-induced late responses and airway hyperresponsiveness. The highest dose of IMA-638 also reduced the early phase response. These findings suggest that IL-13 contributes to allergen-induced airway responses in this sheep model of asthma, and that neutralization of IL-13 is an effective strategy for blocking these A. suum–induced effects.

Key Words: sheep • Ascaris suum • airway hyperresponsiveness • late phase


CLINICAL RELEVANCE

The current study provides the first evidence that IL-13 blockade can be efficacious in a large animal model of respiratory disease. This is a critical milestone supporting the development of IL-13–neutralizing agents for treating human asthma.

 



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J. Pharmacol. Exp. Ther.Home page
M. T. Kasaian, X.-Y. Tan, M. Jin, L. Fitz, K. Marquette, N. Wood, T. A. Cook, J. Lee, A. Widom, R. Agostinelli, et al.
Interleukin-13 Neutralization by Two Distinct Receptor Blocking Mechanisms Reduces Immunoglobulin E Responses and Lung Inflammation in Cynomolgus Monkeys
J. Pharmacol. Exp. Ther., June 1, 2008; 325(3): 882 - 892.
[Abstract] [Full Text] [PDF]




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