Moura Anna Paula V, Santos Luiza C B, Brito Carlos Ramon Nascimento, Valencia Edward, Junqueira Caroline, Filho Adalberto A P, Sant'Anna Mauricio R V, Gontijo Nelder F, Bartholomeu Daniella C, Fujiwara Ricardo T, Gazzinelli Ricardo T, McKay Craig S, Sanhueza Carlos A, Finn M G, Marques Alexandre Ferreira
Instituto de Ciencias Biologicas, Departamento de Parasitologia, Universidade Federal de Minas Gerais, Pampulha, Belo Horizonte, Minas Gerais, Brazil.
Instituto de Pesquisas René Rachou, Fundação Oswaldo Cruz, Belo Horizonte, Minas Gerais, Brazil.
ACS Cent Sci. 2017 Sep 27;3(9):1026-1031. doi: 10.1021/acscentsci.7b00311. Epub 2017 Sep 13.
Secreted and surface-displayed carbohydrates are essential for virulence and viability of many parasites, including for immune system evasion. We have identified the α-Gal trisaccharide epitope on the surface of the protozoan parasites and , the etiological agents of visceral and cutaneous leishmaniasis, respectively, with the latter bearing larger amounts of α-Gal than the former. A polyvalent α-Gal conjugate on the immunogenic Qβ virus-like particle was tested as a vaccine against infection in a C57BL/6 α-galactosyltransferase knockout mouse model, which mimics human hosts in producing high titers of anti-α-Gal antibodies. As expected, α-Gal-T knockout mice infected with promastigotes of both species showed significantly lower parasite load in the liver and slightly decreased levels in the spleen, compared with wild-type mice. Vaccination with Qβ-α-Gal nanoparticles protected the knockout mice against challenge, eliminating the infection and proliferation of parasites in the liver and spleen as probed by qPCR. The α-Gal epitope may therefore be considered as a vaccine candidate to block human cutaneous and visceral leishmaniasis.
分泌型和表面展示型碳水化合物对于许多寄生虫的毒力和生存能力至关重要,包括逃避免疫系统。我们已经在原生动物寄生虫表面鉴定出α-Gal三糖表位,这两种寄生虫分别是内脏利什曼病和皮肤利什曼病的病原体,后者携带的α-Gal比前者更多。在免疫原性Qβ病毒样颗粒上的一种多价α-Gal缀合物,在C57BL/6α-半乳糖基转移酶敲除小鼠模型中作为抗感染疫苗进行了测试,该模型在产生高滴度抗α-Gal抗体方面模拟人类宿主。正如预期的那样,与野生型小鼠相比,感染这两种物种前鞭毛体的α-Gal-T敲除小鼠在肝脏中的寄生虫载量显著降低,脾脏中的水平略有下降。用Qβ-α-Gal纳米颗粒进行疫苗接种可保护敲除小鼠免受攻击,通过qPCR检测发现,这消除了肝脏和脾脏中寄生虫的感染和增殖。因此,α-Gal表位可被视为一种阻断人类皮肤和内脏利什曼病的候选疫苗。