Simons J, Kutubuddin M, Chow M
Department of Applied Biological Sciences, Massachusetts Institute of Technology, Cambridge 02139-4307.
J Virol. 1993 Mar;67(3):1262-8. doi: 10.1128/JVI.67.3.1262-1268.1993.
Poliovirus-specific cellular immune responses were identified in the peripheral blood mononucleocytes of Sabin-immunized human donors by using a proliferation assay. Complement depletion and monoclonal antibody inhibition studies suggest that the effector population is the major histocompatibility complex (MHC) class II-restricted CD4+ T-helper cell. Immune lymphocytes proliferated to polyacrylamide gel purified-capsid proteins VP1, VP2, and VP3 and, in some individuals, to synthetic VP4, indicating the presence of T-cell epitopes in each of these proteins. Using synthetic peptides, T-cell epitopes have been mapped to specific regions in VP1 which lie near previously identified neutralizing antibody recognition sites. Human leukocyte antigen (HLA) typing of the donor individuals indicated that no MHC class II molecule was held in common between all four donor individuals. Thus, the positive responses observed with peptides p182-201 and p244-261 in three of four and four of four donors suggest that these peptides contain epitopes presented by at least two different MHC molecules. Antibody-blocking experiments suggest that an epitope within VP1 residues 244 to 264 is presented by HLA DQ3.
通过增殖试验在接受萨宾疫苗免疫的人类供体的外周血单核细胞中鉴定出脊髓灰质炎病毒特异性细胞免疫反应。补体耗竭和单克隆抗体抑制研究表明,效应细胞群体是主要组织相容性复合体(MHC)II类限制性CD4 + T辅助细胞。免疫淋巴细胞对聚丙烯酰胺凝胶纯化的衣壳蛋白VP1、VP2和VP3增殖,在一些个体中对合成的VP4增殖,表明这些蛋白中均存在T细胞表位。使用合成肽,已将T细胞表位定位到VP1中靠近先前确定的中和抗体识别位点的特定区域。供体个体的人类白细胞抗原(HLA)分型表明,所有四个供体个体之间没有共同的MHC II类分子。因此,在四个供体中的三个和四个供体中的四个中观察到的肽p182 - 201和p244 - 261的阳性反应表明,这些肽包含由至少两种不同MHC分子呈递的表位。抗体阻断实验表明,VP1残基244至264内的一个表位由HLA DQ3呈递。