Leishmania (Leishmania) amazonensis Infection in Mice Treated With FTY720

Autor(es)

Lopes, C. T. ^[1] ; de Paula, D. M. B. ^[2] ; Cury, P. M. ^[3] ; Valero-Lapchik, V. B. ^[2] ; Bueno, V. ^[1]

Afiliação do(s) autor(es)

^[1] Univ Fed Sao Paulo, Dept Med, Div Nephrol, BR-04023900 Sao Paulo - Brazil

^[2] Univ Fed Sao Paulo, Inst Pharmacol, BR-04023900 Sao Paulo - Brazil

^[3] Med Sch Sao Jose do Rio Preto FAMERP, Dept Pathol, Sao Jose Do Rio Preto - Brazil

• Tipo de documento: Artigo Científico
• Fonte: Transplantation Proceedings; v. 42, n. 2, p. 578-581, MAR 2010.
• Citações Web of Science: 2

Resumo

In transplantation, parasite diseases are transmitted from the donor, or appear as de novo infections, or activate from a dormant insource as a consequence of immunosuppression. Clinical findings have shown that an intact immune system is crucial to prevent recurrence of Leishmania infection. We used BALB/c and C57BL/6 mice to evaluate the role of FTY720 in leishmaniasis. Mice inoculated with Leishmania (Leishmania) amazonensis were followed over 71/2 weeks for foot thickness measurements after initiation of FTY720 treatment. After 10 days of treatment, spleen, blood, and the foot were harvested for evaluation. BALB/c showed greater evident foot thickness than C57BL/6 mice. Oral treatment with FTY720 (1 mg/kg/d) over 10 days produced the same outcome. Increases in CD4(+) and CD8(+) T cells were observed after infection; FTY720 treatment was associated with a decrease in CD4(+) T cells only in BALB/c mice, whereas CD8(+) T cells were decreased in both mice strains. CD11b(+) expression decreased after infection with a discrete increase after FTY720 treatment. Lymphopenia was observed among all FTY720-treated mice. In conclusion, we observed that FTY720 produced no worse an outcome as monotherapy in established infections with L (L) amazonensis. (AU)

• Processo FAPESP: 07/56901-5 - Modelos experimentais em transplante
• Beneficiário: Camila Takáo Lopes
• Modalidade de apoio: Bolsas no Brasil - Mestrado
• Processo FAPESP: 04/14727-0 - Uso dos modelos de toxicidade renal e transplante cardíaco para a avaliação da nova droga FTY720
• Beneficiário: Valquiria Bueno
• Modalidade de apoio: Auxílio à Pesquisa - Jovens Pesquisadores