首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Protective Plasmodium knowlesi Mr 74000 antigen in membranes of schizont-infected rhesus erythrocytes
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Protective Plasmodium knowlesi Mr 74000 antigen in membranes of schizont-infected rhesus erythrocytes

机译:裂殖体感染的恒河猴红细胞膜中的保护性知识性疟原虫Mr 74000抗原

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摘要

The immunogenic Plasmodium knowlesi (H strain) Mr 74,000 protein in membranes of schizont-infected rhesus erythrocytes was purified on a large scale, free of other polypeptides as monitored by dodecyl sulfate polyacrylamide gel electrophoresis and isoelectric focusing. In a limited vaccination trial, four rhesus monkeys were immunized four consecutive times with the Mr 74,000 protein and Freund's complete and incomplete adjuvants. Two monkeys were injected with adjuvant only. Upon challenge with 10(4) viable P. knowlesi schizonts of the heterologous W strain, the control monkeys developed fatal parasitemias after 7 d. In contrast, the vaccinated monkeys exhibited a delayed onset of patent parasitemias and underwent self-cure on days 14 to 16 after peak parasitemias of between 7 and 11%. The protective immunity that was induced crossed different strains of P. knowlesi. Blood smears at the time of cure demonstrated limited reinfection, as indicated by the presence of normally appearing ring and trophozoite stages. The absence of schizont stages in the peripheral blood suggested a specific interruption of the erythrocytic schizogony at that stage. Immunochemical analyses of the rhesus sera revealed antibody only against the Mr 74,000 protein after the first two immunizations. Upon repeated antigen injection, antibodies reacted with components of Mr of approximately 102,000, 140,000, and 230,000 in addition to the Mr 74,000 protein. Besides immunological cross-reactivity, relatedness between all four immune-precipitated proteins was indicated by a greater than 50% tryptic peptide homology, suggesting that the Mr 230,000 component represents a precursor protein that is cleaved within the infected erythrocyte into proteins with Mr of approximately 140,000, 102,000, and 74,000.
机译:通过十二烷基硫酸盐聚丙烯酰胺凝胶电泳和等电聚焦监测,大规模纯化了裂殖体感染的恒河猴红细胞膜上的免疫原性疟原虫(H株)Mr 74,000蛋白。在有限的疫苗接种试验中,使用74,000先生蛋白和弗氏完全佐剂和不完全佐剂连续免疫了四只恒河猴四次。两只猴子仅注射了佐剂。在用异源W株的10(4)个活的知识性枯萎病菌挑战后,对照猴子在7天后出现了致命的寄生虫病。相反,接种疫苗的猴子表现出延迟的寄生性寄生虫病发作,并且在寄生率达到7%至11%的峰值后的第14天到第16天进行自治愈。诱导的保护性免疫与诺氏假单胞菌的不同菌株交叉。治愈时的血液涂片显示出有限的再感染,如正常出现的环状和滋养体阶段所示。外周血中无裂殖体阶段,提示该阶段红细胞分裂症的特定中断。恒河猴血清的免疫化学分析显示,在前两次免疫后,仅针对74,000先生蛋白的抗体。反复注射抗原后,抗体与74,000先生蛋白以外的大约102,000、140,000和230,000先生的成分发生反应。除免疫学交叉反应性外,所有四种免疫沉淀蛋白之间的相关性均通过大于50%的胰蛋白酶肽同源性表明,这表明Mr 230,000组分代表一种前体蛋白,该蛋白在被感染的红血球中裂解为Mr约为140,000的蛋白。 ,102,000和74,000。

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