Petersen E, Høgh B, Jakobsen P H, Dziegiel M, Borre M, Jepsen S
Statens Seruminstitut, Parasitologisk Laboratorium, København.
Ugeskr Laeger. 1990 Jul 16;152(29):2092-5.
Traditional malaria control is in a crisis on account of chemo-resistance of Plasmodium falciparum and insecticide-resistance of the malaria mosquito. New ways to control malaria have been opened by the possibility of producing a vaccine. Several malaria proteins (e.g. CSP, gp195, Pf155/RESA, GLURP) have been sequenced and it has been shown that most of the proteins have repetitive units. Analyses of T- and B-cell epitopes show that T-cell epitopes are mainly localized to the non-conserved parts of the antigens. Repeated malaria infections, therefore, may be seen as a number of primary infections, which partly explains the very slow development of immunity to the parasite. The initial three vaccination experiments in humans did not succeed in inducing a complete protection of the individual but it showed that partial immunization is possible.
由于恶性疟原虫的化学抗性和疟蚊的杀虫剂抗性,传统的疟疾控制正处于危机之中。生产疫苗的可能性为控制疟疾开辟了新途径。几种疟疾蛋白质(如CSP、gp195、Pf155/RESA、GLURP)已被测序,结果表明大多数蛋白质都有重复单元。对T细胞和B细胞表位的分析表明,T细胞表位主要定位于抗原的非保守部分。因此,反复的疟疾感染可能被视为多次原发性感染,这部分解释了对该寄生虫的免疫力发展非常缓慢的原因。最初的三次人体疫苗接种实验未能成功诱导个体获得完全保护,但表明部分免疫是可能的。