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Published ahead of print on February 25, 2003, doi:10.1164/rccm.200209-1002OC

Am. J. Respir. Crit. Care Med., Volume 167, Number 10, May 2003, 1393-1399

A more recent version of this article appeared on May 15, 2003
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Submitted on September 6, 2002
Accepted on February 19, 2003

Characterisation of a mouse model of allergy to a major occupational latex glove allergen Hev b 5

Charles L Hardy1*, Linda Kenins1, Alexander C Drew1, Jennifer M Rolland1, and Robyn E O'Hehir2

1 Cooperative Research Centre for Asthma, NSW, Australia; Pathology and Immunology, Monash University, Melbourne, VIC, Australia, 2 Cooperative Research Centre for Asthma, NSW, Australia; Allergy, Asthma and Clinical Immunology, The Alfred Hospital, Melbourne, VIC, Australia

* To whom correspondence should be addressed. E-mail: charles.hardy{at}med.monash.edu.au.

Allergen-specific immunotherapy is a clinically proven effective treatment for many allergic diseases including asthma, however, it is not currently available for latex allergy due to the high risk of anaphylaxis. There is therefore a crucial need for an animal model of latex allergy in which to develop effective immunotherapy. Previous mouse models of latex allergy either did not characterise the allergic pulmonary immune response, or used crude latex extracts, making it difficult to quantify the contribution of individual proteins and limiting their usefulness for developing specific immunotherapy. We immunised mice with recombinant Hev b 5, a defined major latex allergen, or latex glove protein extract, representing the range of occupationally-encountered processed latex allergens. The immune response was compared to that seen in ovalbumin-immunised mice. Immunisation with Hev b 5 or glove extract elicits hallmarks of allergic pulmonary Th2-type immune responses, comparable to those for ovalbumin, including: (1) serum antigen-specific IgE, (2) an eosinophilic inflammatory infiltrate in the lung, (3) increased IL-5 in lung bronchoalveolar lavage fluid, and (4) mucus hypersecretion by epithelial cells in the lung airways. This mouse model will aid the development of potentially curative treatments for latex-sensitised individuals including those with occupational asthma.


Key words: eosinophil, inflammation, interleukins, cytokines




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