Folkard S G, Bianco A E
Liverpool School of Tropical Medicine, UK.
Parasite Immunol. 1995 Oct;17(10):541-53. doi: 10.1111/j.1365-3024.1995.tb00885.x.
Mice inoculated with microfilariae of the filarial nematode Onchocerca lienalis clear their parasites from the skin over a period of 3 to 4 months and are highly resistant to a challenge infection. The adoptive transfer of spleen cells at various time points following primary and secondary infections of mice shows that exposures of 50 days or greater are required for the generation of lymphocytes capable of transferring protection to naive recipients. This adoptive transfer of protection with spleen cells from infection-primed mice partitions with the T lymphocyte population. In contrast, the passive transfer of protection with spleen-derived B cells, or sera taken at various time points following infection was not achieved. Moreover, there was no detectable synergistic effect when B and T cells were co-administered to recipient animals. Depletion of CD4+ and CD8+ T cells with monoclonal antibodies shows that CD8+ T cells have some regulatory effect on parasite establishment early in primary infection, but this is later superseded by CD4+ T cell reactivity that is predominant both when primary infection microfilariae are cleared and also during resistance to reinfection. Measurement of cytokines in the sera of mice undergoing primary and secondary infections support a microfilariae-induced Th2 activity, with high levels of IL-5 that are sustained upon reinfection, and low levels of IFN-gamma that are negligible at the time when mice are most strongly immune.
接种丝状线虫盘尾丝虫微丝蚴的小鼠在3至4个月的时间内将寄生虫从皮肤中清除,并对再次感染具有高度抵抗力。在小鼠初次和二次感染后的不同时间点进行脾细胞的过继转移,结果表明,需要50天或更长时间的暴露才能产生能够将保护作用转移给未感染受体的淋巴细胞。这种来自感染致敏小鼠的脾细胞的保护过继转移与T淋巴细胞群体有关。相比之下,用脾源性B细胞或感染后不同时间点采集的血清进行保护的被动转移未成功。此外,当将B细胞和T细胞共同给予受体动物时,未检测到协同效应。用单克隆抗体清除CD4 +和CD8 + T细胞表明,CD8 + T细胞在初次感染早期对寄生虫的建立有一定的调节作用,但这一作用后来被CD4 + T细胞反应所取代,CD4 + T细胞反应在初次感染微丝蚴被清除时以及再次感染抵抗期间均占主导地位。对经历初次和二次感染的小鼠血清中的细胞因子进行测量,结果支持微丝蚴诱导的Th2活性,再次感染时IL-5水平较高且持续存在,而在小鼠免疫最强时IFN-γ水平较低,可忽略不计。