Pink J R, Rijnbeek A M, Reber-Liske R, Sinigaglia F
Eur J Immunol. 1987 Feb;17(2):193-6. doi: 10.1002/eji.1830170207.
T lymphocyte clones specific for malarial (Plasmodium falciparum) blood stage antigens were obtained from acutely infected patients or from donors living in a malaria-endemic area of West Africa. Thirty-four clones carrying the CD4 antigen, and one CD8+ clone, were tested in a proliferation assay for their capacity to recognize P. falciparum isolates of different geographical origins. Only one clone distinguished between different parasite isolates (it failed to react with a parasite isolate originating from East Africa, but did recognize West African and Asian isolates). All of the clones responded well to intact erythrocytes containing viable parasites, but some responded poorly to extracts of parasitized cells. Eight of 19 clones studied (all CD4+) recognized parasite antigens which had characteristic mobilities in sodium dodecyl sulfate-containing polyacrylamide gels. The antigens had apparent molecular weights of about 20,000, 35,000, 40,000, 120,000, 150,000-200,000 and 200,000. These results (together with a previous report of two clones recognizing an antigen of molecular weight about 50,000, Sinigaglia and Pink, EMBO J. 1985. 4:3819) show that T cells in infected individuals react with at least 6 different parasite proteins.
从急性感染患者或居住在西非疟疾流行地区的供体中获得了针对疟疾(恶性疟原虫)血液阶段抗原的T淋巴细胞克隆。对34个携带CD4抗原的克隆和1个CD8 +克隆进行了增殖试验,以检测它们识别不同地理来源的恶性疟原虫分离株的能力。只有一个克隆能够区分不同的寄生虫分离株(它不与源自东非的寄生虫分离株反应,但能识别西非和亚洲的分离株)。所有克隆对含有活寄生虫的完整红细胞反应良好,但有些对寄生细胞提取物反应不佳。在研究的19个克隆中(均为CD4 +),有8个克隆识别在含十二烷基硫酸钠的聚丙烯酰胺凝胶中具有特征迁移率的寄生虫抗原。这些抗原的表观分子量约为20,000、35,000、40,000、120,000、150,000 - 200,000和200,000。这些结果(连同之前关于两个克隆识别分子量约为50,000的抗原的报告,Sinigaglia和Pink,《欧洲分子生物学组织杂志》。1985年。4:3819)表明,感染个体中的T细胞与至少6种不同的寄生虫蛋白发生反应。