Chauhan V S, Chatterjee S, Johar P K
International Centre for Genetic Engineering & Biotechnology, New Delhi, India.
Parasite Immunol. 1993 Apr;15(4):239-42. doi: 10.1111/j.1365-3024.1993.tb00606.x.
Two synthetic polypeptides containing multiple B- and T-cell epitopes derived from the conserved regions of two vaccine candidate antigens namely MSA-1 and RESA of human malarial parasite P. falciparum were studied for immunogenicity and protectivity. Both constructs elicited strong antibody and lymphocyte proliferation responses in BALB/c mice immunized with the carrier-free peptides. In an ELISA, these peptides also bound antibodies present in the sera from the P. vivax infected humans as well as from the P. yoelii infected mice. Significantly, our data showed that immunization of mice with these P. falciparum peptide could impart partial protection against P. yoelii challenge infection. Our finding that synthetic peptides representing portions of P. falciparum antigens were capable of stimulating protective immune responses against rodent malaria suggests that murine malaria model P. yoelii may provide a suitable system for primary screening of potentially protective synthetic immunogens.
研究了两种合成多肽的免疫原性和保护作用,这两种多肽含有源自两种候选疫苗抗原(即恶性疟原虫的MSA-1和RESA)保守区域的多个B细胞和T细胞表位。在无载体肽免疫的BALB/c小鼠中,这两种构建体均引发了强烈的抗体和淋巴细胞增殖反应。在酶联免疫吸附测定(ELISA)中,这些肽还能结合间日疟原虫感染人类以及约氏疟原虫感染小鼠血清中的抗体。重要的是,我们的数据表明,用这些恶性疟原虫肽免疫小鼠可对约氏疟原虫攻击感染提供部分保护。我们发现代表恶性疟原虫抗原部分的合成肽能够刺激针对啮齿动物疟疾的保护性免疫反应,这表明约氏疟原虫鼠疟模型可能为潜在保护性合成免疫原的初步筛选提供一个合适的系统。