Herrera S, Escobar P, de Plata C, Avila G I, Corradin G, Herrera M A
Department of Microbiology, School of Health, Universidad del Valle, Cali, Colombia.
J Immunol. 1992 Jun 15;148(12):3986-90.
In order to identify T cell epitopes recognized by human in the Plasmodium vivax circumsporozoite protein, 28 overlapping synthetic peptides spanning the entire circumsporozoite protein were tested for their ability to stimulate proliferation of PBMC from 22 adults living in a malaria-endemic area of the Colombian Pacific Coast and from four individuals who never had a history of malaria infection. In addition, BALB/c mice were immunized with pools of peptides, and their lymph node cells were stimulated in vitro with individual peptides. Four epitopes were recognized by human lymphocytes but not all of them by mice. One of the epitopes was located inside the central repetitive B cell immunodominant domain. Several of the variants of the repeats were recognized by about one-third of the studied individuals. Another T cell epitope was located in the amino terminus and the other two in the carboxyl region. Peptides were recognized by both immune and nonimmune donors. Some of them were frequently recognized suggesting a lack of genetic restriction, whereas some others were recognized by only a few individuals but induced strong proliferation. These epitopes may be of potential value for a malaria subunit vaccine.
为了鉴定人类在间日疟原虫环子孢子蛋白中识别的T细胞表位,对覆盖整个环子孢子蛋白的28个重叠合成肽进行了测试,以检测它们刺激来自哥伦比亚太平洋沿岸疟疾流行地区的22名成年人以及4名无疟疾感染史个体的外周血单核细胞(PBMC)增殖的能力。此外,用肽池免疫BALB/c小鼠,并用单个肽在体外刺激它们的淋巴结细胞。人类淋巴细胞识别出4个表位,但小鼠并非全部识别。其中一个表位位于中央重复B细胞免疫显性结构域内。约三分之一的研究个体识别出了几种重复序列变体。另一个T细胞表位位于氨基末端,另外两个位于羧基区域。免疫和非免疫供体均可识别这些肽。其中一些肽经常被识别,表明缺乏基因限制,而另一些肽仅被少数个体识别,但能诱导强烈增殖。这些表位可能对疟疾亚单位疫苗具有潜在价值。