Roopenian D C, Anderson P S
Jackson Laboratory, Bar Harbor, ME 04609.
J Immunol. 1988 Jul 15;141(2):391-7.
The role of L3T4+ (CD4+) Th cells in generation of CTL specific for discrete minor histocompatibility Ag was investigated. Suppression of the function of Th cells in vivo by chronic treatment with anti-L3T4 mAb prevented congenic strains of mice from being primed and from generating CTL specific for Ag encoded by the minor histocompatibility loci--H-3, H-1, and B2m. Analysis of proliferative responses and lymphokine secretion of cells from animals primed with one of these minor H Ag, beta 2-microglobulin, but not treated with anti-L3T4 antibodies, indicated that L3T4- class I MHC-restricted T cells were themselves responsible for the very great majority of the observed minor H Ag-specific proliferation and secretion of lymphokines associated with both T cell proliferation and activation of CTL. All together, the data indicate that in responses against discrete minor H Ag, L3T4+Th-independent CTL are generated through an L3T4+Th-dependent pathway.
研究了L3T4 +(CD4 +)Th细胞在产生针对离散次要组织相容性抗原的CTL中的作用。通过用抗L3T4单克隆抗体进行长期治疗在体内抑制Th细胞功能,可防止同基因小鼠品系被致敏,并防止产生针对由次要组织相容性位点-H-3、H-1和B2m编码的抗原的CTL。对用这些次要H抗原之一、β2-微球蛋白致敏但未用抗L3T4抗体处理的动物的细胞增殖反应和淋巴因子分泌进行分析,结果表明,L3T4 + I类MHC限制性T细胞本身对绝大多数观察到的次要H抗原特异性增殖以及与T细胞增殖和CTL激活相关的淋巴因子分泌负责。总之,数据表明在针对离散次要H抗原的反应中,独立于L3T4 + Th的CTL是通过依赖L3T4 + Th的途径产生的。