Defining a Link with Asthma in Mice Congenitally Deficient in Eosinophils

Author:

Lee James J.12345,Dimina Dawn12345,Macias MiMi P.12345,Ochkur Sergei I.12345,McGarry Michael P.12345,O'Neill Katie R.12345,Protheroe Cheryl12345,Pero Ralph12345,Nguyen Thanh12345,Cormier Stephania A.12345,Lenkiewicz Elizabeth12345,Colbert Dana12345,Rinaldi Lisa12345,Ackerman Steven J.12345,Irvin Charles G.12345,Lee Nancy A.12345

Affiliation:

1. Division of Pulmonary Medicine, Mayo Clinic Arizona, Scottsdale, AZ 85259, USA.

2. Department of Biochemistry and Molecular Biology, Mayo Clinic Arizona, Scottsdale, AZ 85259, USA.

3. Division of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, AZ 85259, USA.

4. Vermont Lung Center, Department of Medicine, University of Vermont, Burlington, VT 05405, USA.

5. Department of Biochemistry and Molecular Biology, University of Illinois, College of Medicine, Chicago, IL 60612, USA.

Abstract

Eosinophils are often dominant inflammatory cells present in the lungs of asthma patients. Nonetheless, the role of these leukocytes remains poorly understood. We have created a transgenic line of mice (PHIL) that are specifically devoid of eosinophils, but otherwise have a full complement of hematopoietically derived cells. Allergen challenge of PHIL mice demonstrated that eosinophils were required for pulmonary mucus accumulation and the airway hyperresponsiveness associated with asthma. The development of an eosinophil-less mouse now permits an unambiguous assessment of a number of human diseases that have been linked to this granulocyte, including allergic diseases, parasite infections, and tumorigenesis.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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