Jones W C, Barnard A L, Slade A, Mills K H
National Institute for Biological Standards and Control, South Mimms, Potters Bar, Herts, UK.
J Immunol. 1992 Nov 1;149(9):3120-6.
CD4+ T cell recognition of the simian immunodeficiency virus (SIV) surface envelope (env) glycoprotein was examined by using a panel of 10 T cell lines and 4 T cell clones derived from 10 individual macaques immunized with inactivated SIV or recombinant SIV env proteins. The results demonstrated that CD4+ T cells from each animal recognized between 1 and 7 peptides in 4 distinct regions of the protein including both variable and conserved domains. MLR of PBMC from selected macaques together with RFLP analysis by using the HLA DR beta probes suggested that animals of distinct MHC class II haplotypes can recognize identical peptides. These T cell epitopes within conserved regions of the envelope protein, together with identified linear B cell epitopes recognized by neutralizing antibodies, may be relevant in vaccine design.
利用一组10个T细胞系和4个T细胞克隆,对来自10只经灭活的猴免疫缺陷病毒(SIV)或重组SIV包膜(env)蛋白免疫的猕猴的CD4 + T细胞对SIV表面env糖蛋白的识别情况进行了检测。结果表明,每只动物的CD4 + T细胞在该蛋白的4个不同区域(包括可变区和保守区)识别1至7个肽段。选用猕猴的外周血单核细胞进行混合淋巴细胞反应(MLR),并使用HLA DRβ探针进行限制性片段长度多态性(RFLP)分析,结果表明不同MHC II类单倍型动物可识别相同的肽段。包膜蛋白保守区内的这些T细胞表位,连同已确定的可被中和抗体识别的线性B细胞表位,可能与疫苗设计相关。