Franks Simon, Baton Luke, Tetteh Kevin, Tongren Eric, Dewin David, Akanmori Bartholomew D, Koram Kojo A, Ranford-Cartwright Lisa, Riley Eleanor M
Institute of Cell, Animal and Population Biology, University of Edinburgh, United Kingdom.
Infect Immun. 2003 Jun;71(6):3485-95. doi: 10.1128/IAI.71.6.3485-3495.2003.
Diversity in the surface antigens of malaria parasites is generally assumed to be a mechanism for immune evasion, but there is little direct evidence that this leads to evasion of protective immunity. Here we show that alleles of the highly polymorphic merozoite surface protein 2 (MSP-2) can be grouped (within the known dimorphic families) into distinct serogroups; variants within a serogroup show extensive serological cross-reactivity. Cross-reactive epitopes are immunodominant, and responses to them may be boosted at the expense of responses to novel epitopes (original antigenic sin). The data imply that immune selection explains only some of the diversity in the msp-2 gene and that MSP-2 vaccines may need to include only a subset of the known variants in order to induce pan-reactive antibodies.
疟原虫表面抗原的多样性通常被认为是一种免疫逃避机制,但几乎没有直接证据表明这会导致逃避保护性免疫。在这里,我们表明,高度多态的裂殖子表面蛋白2(MSP-2)的等位基因可以(在已知的双态家族内)分为不同的血清群;一个血清群内的变体显示出广泛的血清学交叉反应性。交叉反应性表位具有免疫优势,对它们的反应可能会以牺牲对新表位的反应为代价而增强(原始抗原罪)。这些数据表明,免疫选择只能解释msp-2基因多样性的一部分,并且MSP-2疫苗可能只需要包含已知变体的一个子集,以诱导泛反应性抗体。