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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Experimental autoimmune encephalomyelitis can be prevented and cured by infection with Trypanosoma cruzi

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Autor(es):
Tadokoro, Carlos E. ; Vallochi, Adriana L. ; Rios, Lília S. ; Martins, Gislâine A. ; Schlesinger, David ; Mosca, Tainá ; Kuchroo, Vijay K. ; Rizzo, Luiz V. ; Abrahamsohn, Ises A. [9]
Número total de Autores: 9
Tipo de documento: Artigo Científico
Fonte: Journal of Autoimmunity; v. 23, n. 2, p. 103-115, Sept. 2004.
Área do conhecimento: Ciências Biológicas - Imunologia
Assunto(s):Toxoplasmose ocular   Citocinas   Trypanosoma cruzi
Resumo

Trypanosoma cruzi is an intracellular parasite that induces a strong Th1-type response and immunosuppression during the acute phase of infection. To study how the infection with T. cruzi would modulate the development of an autoimmune disease, we immunized C57BL/6 mice and IL-10 or iNOS knock-out mice of the same background with the encephalitogenic MOG 35-55 peptide and infected them with T. cruzi. Our results demonstrate that infection with T. cruzi completely prevents EAE development and furthermore induces complete and lasting remission in mice that were infected with this parasite after they had developed clinical EAE. Nitric oxide and IL-10 participate in triggering the mechanisms associated with EAE suppression by the infection. Decreased lymphoproliferation and increased frequencies of Annexin-positive cells and of T cells bearing CD95, CD95L or CTLA-4 were observed in the spleen from immunized/infected mice, as well as lower IL-2 and increased TGF-beta production in comparison with only immunized mice. Our results indicate that several effector and regulatory mechanisms of the immune response that arise during the acute phase of T. cruzi infection lastingly affect the expansion and/or effector functions of encephalitogenic cells, preventing the onset or inducing complete remission of EAE. (AU)

Processo FAPESP: 97/11949-7 - Imunossupressao: mecanismo de controle da autoreatividade na doenca de chagas?
Beneficiário:Carlos Eduardo Tadokoro
Linha de fomento: Bolsas no Brasil - Doutorado