Link H T, White K, Krzych U
Department of Biology, Catholic University of America, Washington, D.C.
Eur J Immunol. 1993 Sep;23(9):2263-9. doi: 10.1002/eji.1830230932.
The mechanism of malaria protective immunity induced by immunization with radiation-attenuated Plasmodium sporozoites (SPZ) is only partially understood. For example, B and T cell responses specific for the circumsporozoite (CS) protein, a 46 kDa SPZ surface protein, have been characterized; however, events leading to SPZ-specific T cell activation, i.e., processing and presentation of SPZ by antigen-presenting cells have not been investigated. In the present study we describe the in vitro analysis of requirements for accessory cell function in the presentation of SPZ to SPZ-immune T cells. The results establish that SPZ-induced proliferative T cells are reactive to non-processed SPZ presented by activated B cells and, thus, imply that the non-processed form of the SPZ-associated CS protein restricts the induction of the potential CS protein T cell repertoire.
用辐射减毒疟原虫子孢子(SPZ)免疫诱导疟疾保护性免疫的机制仅得到部分理解。例如,针对环子孢子(CS)蛋白(一种46 kDa的SPZ表面蛋白)的B细胞和T细胞应答已得到表征;然而,导致SPZ特异性T细胞活化的事件,即抗原呈递细胞对SPZ的加工和呈递尚未得到研究。在本研究中,我们描述了对辅助细胞功能在将SPZ呈递给SPZ免疫T细胞中的需求的体外分析。结果表明,SPZ诱导的增殖性T细胞对活化B细胞呈递的未加工SPZ有反应,因此,这意味着SPZ相关CS蛋白的未加工形式限制了潜在CS蛋白T细胞库的诱导。