Weiss W R
Infectious Disease Department, Naval Medical Research Institute, Bethesda, MD.
Immunol Lett. 1990 Aug;25(1-3):39-42. doi: 10.1016/0165-2478(90)90088-8.
We compare and contrast the results of immunizing mice with irradiated sporozoites of Plasmodium berghei and Plasmodium yoelii. Host genetic control of protective immunity is different in the two rodent malarias. Few mouse strains are strongly protected by P. yoelii sporozoites, while all are protected by P. berghei sporozoite immunization. The role of CD8+ T cells in the protective immune response to each of these malarias varies with the strain of mouse. Moreover, a single strain will use a CD8+ T cell-dependent mechanism against one malaria, and a CD8+ independent mechanism against the other. Thus, each host-parasite pairing in these rodent malarias engenders a unique set of immune responses. Such variety should be expected in the immune response to the human malarias, and may complicate the development of universally applicable vaccines.
我们比较并对比了用伯氏疟原虫和约氏疟原虫的辐照子孢子免疫小鼠的结果。在这两种啮齿动物疟疾中,保护性免疫的宿主基因控制有所不同。很少有小鼠品系能被约氏疟原虫子孢子强烈保护,而所有品系都能通过伯氏疟原虫子孢子免疫得到保护。CD8 + T细胞在针对每种疟疾的保护性免疫反应中的作用因小鼠品系而异。此外,单一品系对一种疟疾会采用依赖CD8 + T细胞的机制,而对另一种疟疾则采用不依赖CD8 + T细胞的机制。因此,这些啮齿动物疟疾中的每一种宿主 - 寄生虫配对都会引发一组独特的免疫反应。在对人类疟疾的免疫反应中也应预期会有这种多样性,这可能会使通用疫苗的研发变得复杂。