Lehner T, Avery J, Smith R
Immunology. 1985 Apr;54(4):701-11.
We have utilized the antigen-binding function of a subset of T8+ cells to remove these cells in vitro from human peripheral blood mononuclear cells. This was carried out by treating the cells with streptococcal antigen (SA), monoclonal anti-SA antibody and complement. The concentration of SA binding to T8+ cells differs with the HLA-DR type of the cells: 1 ng SA binds to DRw6+ cells and elicits T helper activity, whereas 1000 ng SA elicits T suppressor activity, in an assay for antibody-forming cells. After depletion of the antigen-binding cells by the SA-specific complement-dependent killing technique, the helper function of the DRw6+ cells was lost but suppression was elicited not only by 1000 ng but also by 1 ng SA. Similarly, DRw6- cells which bind 1000 ng SA to elicit helper activity and 1 ng to elicit suppression, when depleted of the SA-binding cells, resulted in loss of helper activity but again, suppression could be elicited by both 1000 and 1 ng SA. We suggest that treatment of mononuclear cells with antigen, the specific antibody and complement removes the T8+ antigen-binding cells which present antigen to T helper cells and results in the loss of helper function. Suppressor function is however, not only retained with the original concentration of SA but also expressed with that required to elicit helper function in the untreated cells. These findings are consistent with our hypothesis that the antigen-binding and presenting T8+ cells also function as contrasuppressor cells. Thus, the T8+ subset of cells have a dual function, to present antigen and to activate T helper cell function, and to prevent suppressor cells from inhibiting the helper cells.
我们利用T8 +细胞亚群的抗原结合功能,在体外从人外周血单个核细胞中去除这些细胞。这是通过用链球菌抗原(SA)、抗SA单克隆抗体和补体处理细胞来实现的。与T8 +细胞结合的SA浓度因细胞的HLA - DR类型而异:在抗体形成细胞测定中,1 ng SA与DRw6 +细胞结合并引发T辅助活性,而1000 ng SA引发T抑制活性。通过SA特异性补体依赖性杀伤技术耗尽抗原结合细胞后,DRw6 +细胞的辅助功能丧失,但不仅1000 ng SA而且1 ng SA都能引发抑制作用。同样,结合1000 ng SA引发辅助活性和1 ng SA引发抑制作用的DRw6 -细胞,在耗尽SA结合细胞后,导致辅助活性丧失,但同样,1000 ng和1 ng SA都能引发抑制作用。我们认为,用抗原、特异性抗体和补体处理单个核细胞可去除将抗原呈递给T辅助细胞的T8 +抗原结合细胞,并导致辅助功能丧失。然而,抑制功能不仅在SA原始浓度下得以保留,而且在未处理细胞中引发辅助功能所需的浓度下也能表达。这些发现与我们的假设一致,即抗原结合和呈递的T8 +细胞也作为抗抑制细胞发挥作用。因此,T8 +细胞亚群具有双重功能,即呈递抗原并激活T辅助细胞功能,以及防止抑制细胞抑制辅助细胞。