Lehner T, Jones T
Immunology. 1984 Oct;53(2):215-25.
Binding of streptococcal antigen was compared between T8+ cells and monocytes (Mo) from DRw6+ and DRw6- subjects. Both T8+ cells and Mo from DRw6- subjects bind streptococcal antigen (SA) specifically and almost entirely at a concentration of 1000 ng per 0.1 ml. However, the DRw6+, T8+ cells bind SA at a concentration of 1 ng but the DRw6+ Mo bind SA at both 1 and 1000 ng of SA per 0.1 ml. The HLA-DR-dependent shift in the binding concentration of SA applied to Mo as well as T8+ cells, except that the DRw6+ Mo showed a biphasic response (1 and 1000 ng) of SA binding. Comparative inhibition studies revealed that the antigen binding T8+ cells, unlike Mo, are inhibited with monoclonal anti-T8 and -T5 antibodies and anti-suppressor factor antiserum. Neither cell was inhibited by anti- T4, M1, F(ab), IgG, IgM, VH null cell or helper factor antibodies, and anti-T3 antibodies showed variable inhibition of SA binding to T8+ cells but no inhibition to Mo. A functional comparison was carried out between the antigen binding cells and helper and suppressor activities in unseparated mononuclear cells. T4-depleted and T8-depleted populations of cells. The concentration of SA binding to the T8+ cells was the same as that required to elicit helper activity but reciprocal to the broad range of SA concentrations necessary to induce suppressor cell activity. The results are interpreted on the basis of the hypothesis that the antigen binding T8+ cell functions as a contrasuppressor cell which prevents the major subset of the T8+ cells inhibiting the T4+ cells.
比较了DRw6阳性和DRw6阴性受试者的T8 +细胞与单核细胞(Mo)之间链球菌抗原的结合情况。DRw6阴性受试者的T8 +细胞和Mo在每0.1 ml 1000 ng的浓度下都能特异性且几乎完全地结合链球菌抗原(SA)。然而,DRw6阳性的T8 +细胞在1 ng的浓度下就能结合SA,而DRw6阳性的Mo在每0.1 ml 1 ng和1000 ng的SA浓度下都能结合SA。应用于Mo以及T8 +细胞的SA结合浓度存在HLA - DR依赖性变化,只是DRw6阳性的Mo对SA结合表现出双相反应(1 ng和1000 ng)。比较抑制研究表明,与Mo不同,抗原结合性T8 +细胞可被单克隆抗T8和抗T5抗体以及抗抑制因子抗血清所抑制。两种细胞均未被抗T4抗体M1、F(ab)、IgG、IgM、VH阴性细胞或辅助因子抗体所抑制,抗T3抗体对SA与T8 +细胞的结合表现出可变的抑制作用,但对Mo无抑制作用。对未分离的单核细胞、T4缺失和T8缺失细胞群体中的抗原结合细胞与辅助和抑制活性进行了功能比较。与T8 +细胞结合的SA浓度与引发辅助活性所需的浓度相同,但与诱导抑制细胞活性所需的广泛SA浓度范围呈反比。基于抗原结合性T8 +细胞作为反抑制细胞发挥作用的假设对结果进行了解释,该反抑制细胞可防止T8 +细胞的主要亚群抑制T4 +细胞。