Faculdade de Farmácia, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
Curr Opin Microbiol. 2012 Aug;15(4):476-85. doi: 10.1016/j.mib.2012.05.002. Epub 2012 Jun 13.
Visceral leishmaniasis is a major health problem in Latina America, as well as the Mediterranean region of Europe and Asia. We aimed to develop a vaccine against visceral leishmaniasis targeting the intracellular amastigotes, which is the parasite stage that persists throughout infections with Leishmania parasites. With this in mind, we identified an amastigote specific antigen (A2) that contains an immunogenic epitope for CD4+ T helper (Th) cells and multiple repetitive units encoding CD8+ cytotoxic T lymphocyte (CTL) epitopes. Vaccine formulations containing the recombinant A2 associated with saponin, alum and IL-12 or expressed by attenuated adenovirus were shown to be protective in mice, dogs and nonhuman-primates. We are currently identifying novel amastigote specific immunogenic proteins that could be aggregated to A2 to further improve the level of vaccine-induced cell-mediated immunity and protection against visceral leishmaniasis.
内脏利什曼病是拉丁美洲、欧洲地中海地区和亚洲的一个主要卫生问题。我们旨在针对内脏利什曼原虫的内阿米巴阶段(即寄生虫在利什曼原虫感染期间持续存在的阶段)开发一种针对内脏利什曼病的疫苗。考虑到这一点,我们鉴定了一种内阿米巴特异性抗原(A2),它包含针对 CD4+辅助性 T 细胞(Th)细胞的免疫原性表位和多个编码 CD8+细胞毒性 T 淋巴细胞(CTL)表位的重复单元。含有与皂苷、明矾和 IL-12 相关的重组 A2 的疫苗制剂或由减毒腺病毒表达的疫苗制剂在小鼠、狗和非人类灵长类动物中显示出保护作用。我们目前正在鉴定新的内阿米巴特异性免疫原性蛋白,这些蛋白可以与 A2 聚集,以进一步提高疫苗诱导的细胞介导免疫和预防内脏利什曼病的水平。