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(Journal of Leukocyte Biology. 2001;69:353-360.)
© 2001 by Society for Leukocyte Biology

Eosinophil recruitment into sites of delayed-type hypersensitivity reactions in mice

Mauro M. Teixeira*, André Talvani*, Wagner L. Tafuri{dagger}, Nicholas W. Lukacs{ddagger} and Paul G. Hellewell§


* Immunopharmacology Laboratory, Department of Biochemistry and Immunology, and
{dagger} Department of Pathology, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil;
{ddagger} Department of Pathology, University of Michigan, Ann Arbor, Michigan; and
§ Cardiovascular Research Group, University of Sheffield, United Kingdom

Correspondence: Mauro Martins Teixeira, M.D., Ph.D., Immunopharmacology, Departamento de Bioquímica e Imunologia, Instituto de Ciencias Biologicas, Universidade Federal de Minas Gerais, Av. Antonio Carlos, 6627—Pampulha, 31270-901 Belo Horizonte MG Brasil. E-mail: mmtex{at}icb.ufmg.br

The selective accumulation of eosinophils in tissue is a characteristic feature of allergic diseases where there is a predominance of lymphocytes expressing a Th2 phenotype. In an attempt to define factors determining specific eosinophil accumulation in vivo, we have used a radiolabeled technique to assess the occurrence and the mechanisms underlying 111In-eosinophil recruitment into Th1- and Th2-predominant, delayed-type hypersensitivity (DTH) reactions. Eosinophils were purified from the blood of IL-5 transgenic mice, labeled with 111In and injected into nontransgenic CBA/Ca mice. Th1- and Th2-predominant, DTH reactions were induced in mice by immunization with methylated bovine serum albumin (MBSA) in Freund’s complete adjuvant or with Schistosoma mansoni eggs, respectively. In these animals, 111In-eosinophils were recruited in skin sites in an antigen-, time-, and concentration-dependent manner. Depletion of CD4+ lymphocytes abrogated 111In-eosinophil recruitment in both reactions. Pretreatment of animals with anti-IFN-{gamma} mAb abrogated 111In-eosinophil recruitment in MBSA-immunized and -challenged animals, whereas anti-IL-4 inhibited 111In-eosinophil recruitment in both models. Local pretreatment with an anti-eotaxin polyclonal antibody inhibited the MBSA and SEA reactions by 51% and 39%, respectively. These results demonstrate that, although eosinophilia is not a feature of Th1-predominant, DTH reactions, these reactions produce the necessary chemoattractants and express the necessary cell adhesion molecules for eosinophil migration. The control of the circulating levels of eosinophils appears to be a most important strategy in determining tissue eosinophilia.

Key Words: chemokines • bone marrow • interleukin-4 • lymphocytes




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