Taylor-Robinson A W, Phillips R S, Severn A, Moncada S, Liew F Y
Wellcome Laboratories for Experimental Parasitology, University of Glasgow, United Kingdom.
Science. 1993 Jun 25;260(5116):1931-4. doi: 10.1126/science.8100366.
CD4+ T cells play a major role in protective immunity against the blood stage of malaria, but the mechanism of protection is unclear. By adoptive transfer of cloned T cell lines, direct evidence is provided that both TH1 and TH2 subsets of CD4+ T cells can protect mice against Plasmodium chabaudi chabaudi infection. TH1 cells protect by a nitric oxide-dependent mechanism, whereas TH2 cells protect by the enhancement and accelerated production of specific immunoglobulin G1 antibody.
CD4+ T细胞在针对疟疾血液阶段的保护性免疫中发挥主要作用,但保护机制尚不清楚。通过克隆T细胞系的过继转移,提供了直接证据表明CD4+ T细胞的TH1和TH2亚群均可保护小鼠免受恰氏疟原虫感染。TH1细胞通过一氧化氮依赖性机制发挥保护作用,而TH2细胞则通过增强和加速特异性免疫球蛋白G1抗体的产生来发挥保护作用。