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Int Arch Allergy Immunol ; 114 Suppl 1: 45-50, 1997 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-9363925

RESUMO

Nippostrongylus brasiliensis infection is characterized by blood and tissue eosinophilia induced by interleukin (IL)-5 secreted from CD4+ T cells. However, it is still obscure whether eosinophils play an important role in the protection against N. brasiliensis infection. In this study we attempted to determine whether the in vivo environment of IL-5 transgenic mice, characterized by high eosinophil production, could affect the worm burden after N. brasiliensis infection. Kinetic studies on the infection demonstrated a significantly lower worm recovery from the intestine of IL-5 transgenic mice compared to age-matched background controls. This tendency was also observed at the lung stage of the infection. Furthermore, with respect to elevation of the serum IgE concentration, the peak level was observed at 2 weeks after infection in infected background control mice with four times higher concentrations than those of uninfected mice. In contrast, the increase of IgE concentration in IL-5 transgenic mice was very limited and low. The adoptive transfer of eosinophils from IL-5 transgenic mice into background control animals resulted in the reduction of worm recovery from the lungs, suggesting that eosinophils play a key role in the protection against migrating larvae of N. brasiliensis. These results indicate that the innate high level of eosinophils due to constitutive production of IL-5 augments immunity against N. brasiliensis infection.


Assuntos
Eosinófilos/imunologia , Interleucina-5/imunologia , Nippostrongylus/imunologia , Infecções por Strongylida/imunologia , Transferência Adotiva , Animais , Anticorpos Anti-Helmínticos/sangue , Movimento Celular , Eosinofilia/imunologia , Eosinófilos/citologia , Eosinófilos/transplante , Imunoglobulina E/sangue , Interleucina-5/genética , Larva/imunologia , Contagem de Leucócitos , Pulmão/parasitologia , Camundongos , Camundongos Endogâmicos C3H , Camundongos Endogâmicos C57BL , Camundongos Transgênicos , Células Th2/imunologia
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