Brown K N, Jarra W, Newbold C I, Schryer M
Ann Inst Pasteur Immunol (1985). 1985 Jan-Feb;136C(1):11-23.
Cloned lines of the rodent malaria parasite Plasmodium chabaudi (denoted AS and CB) have been used to investigate the strain specificity of immunity to malaria. One defined difference between these lines is their expression of serologically and structurally distinct forms of an Mr 250Kd parasite-encoded antigen. This antigen is a member of a family of schizont/merozoite-associated polypeptides which have been implicated in the induction of protective immunity to rodent, simian and human malaria parasites. CBA/Ca mice were immunized by either (a) purified P. chabaudi AS-250Kd antigen, (b) chronic AS infection or (c) irradiated nonreplicating AS-parasitized erythrocytes. Post-immunization sera were examined by immunoprecipitation of 35S-methionine-labelled parasites, and the mice challenged with either AS or CB parasites. On challenge, mice developed a parasitaemia, the level of which was determined in part by isolate specificity, but only mice in groups (b) and (c) later developed a response which transcended AS/CB differences. The implications of these findings for the nature of exposed parasite antigens and the induction of protective immunity to malaria is discussed.
啮齿动物疟原虫恰氏疟原虫(分别标记为AS和CB)的克隆株已被用于研究疟疾免疫的菌株特异性。这些株系之间一个明确的差异在于它们表达的一种分子量为250Kd的寄生虫编码抗原,其在血清学和结构上有不同形式。该抗原是裂殖体/裂殖子相关多肽家族的一员,这些多肽与诱导针对啮齿动物、猿猴和人类疟原虫的保护性免疫有关。CBA/Ca小鼠通过以下方式免疫:(a)纯化的恰氏疟原虫AS-250Kd抗原,(b)慢性AS感染,或(c)经辐射的无繁殖能力的AS寄生红细胞。免疫后的血清通过对35S-甲硫氨酸标记的寄生虫进行免疫沉淀来检测,然后用AS或CB寄生虫对小鼠进行攻击。在攻击时,小鼠出现了寄生虫血症,其水平部分由分离株特异性决定,但只有(b)组和(c)组的小鼠后来产生了超越AS/CB差异的反应。本文讨论了这些发现对暴露的寄生虫抗原性质以及疟疾保护性免疫诱导的意义。