We report the first synthetic peptide vaccine eliciting strong CD8(+) and CD4(+) T lymphocyte responses in humans. The vaccine, representing the C-terminal region of the circumsporozoite protein of Plasmodium falciparum (amino acids 282-383) was well tolerated and strong sporozoite-specific antibodies were elicited. In addition, robust lymphocyte proliferation responses were equally elicited with concomitant in vitro production of IFN-gamma, crucial in the elimination of the parasite. Most importantly, we also observed the development of CD8(+) T lymphocyte responses decisive in the immunity to malaria. The latter finding opens new, possibly safer, avenues for vaccination strategies when a CD8(+) T cell response is needed.

译文

我们报告了第一个合成肽疫苗,在人类中引起强烈的CD8 () 和CD4 () T淋巴细胞反应。代表恶性疟原虫环子孢子蛋白 (氨基酸282-383) 的C末端区域的疫苗具有良好的耐受性,并产生了强的子孢子特异性抗体。此外,伴随IFN-γ 的体外产生同样引起了强大的淋巴细胞增殖反应,这对于消除寄生虫至关重要。最重要的是,我们还观察到CD8 () T淋巴细胞反应的发展对疟疾的免疫力起决定性作用。当需要CD8(+) T细胞应答时,后者的发现为疫苗接种策略开辟了新的,可能更安全的途径。

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