Sinigaglia F, Guttinger M, Gillessen D, Doran D M, Takacs B, Matile H, Trzeciak A, Pink J R
Central Research Units, F. Hoffmann-La Roche & Co. Ltd., Basel, Switzerland.
Eur J Immunol. 1988 Apr;18(4):633-6. doi: 10.1002/eji.1830180422.
The circumsporozoite protein of the malaria parasite Plasmodium falciparum contains regions of nonrepetitive sequences which are predicted to be T cell recognition sites. We synthesized peptides corresponding to three of these regions, and tested their ability to stimulate proliferation of peripheral blood lymphocytes from donors living in a malaria-endemic area, or from nonimmune donors. Cells from 15 out of 22 donors (including 4 of 6 nonimmune individuals) were stimulated by one or more of the peptides. T cell clones specific for one of the peptides were obtained and shown to recognize the native protein purified from sporozoites. These data help to identify T cell epitopes which could be incorporated into a malaria vaccine.
恶性疟原虫的环子孢子蛋白含有非重复序列区域,这些区域被预测为T细胞识别位点。我们合成了与其中三个区域相对应的肽,并测试了它们刺激来自疟疾流行地区的供体或非免疫供体的外周血淋巴细胞增殖的能力。22名供体中有15名(包括6名非免疫个体中的4名)的细胞受到一种或多种肽的刺激。获得了对其中一种肽具有特异性的T细胞克隆,并证明它们能够识别从子孢子中纯化的天然蛋白。这些数据有助于识别可纳入疟疾疫苗的T细胞表位。