Noble A, Pestano G A, Cantor H
Department of Cancer Immunology and AIDS, Dana Farber Cancer Institute, Boston, MA 02115, USA.
J Immunol. 1998 Jan 15;160(2):559-65.
Stimulation of mature CD4 cells through the TCR induces cellular activation and expansion that are often followed by clonal elimination by a form of apoptosis termed activation-induced cell death. This process of CD4 cell apoptosis is generally thought to reflect clonal suicide and to be independent of other cell types. Here we show that during the response to the superantigen Staphylococcal enterotoxin A, activated CD8 cells, but not activated CD4 cells, suppress the CD4 proliferative response. Suppression by CD8 cells reflects their ability to induce CD4 cell apoptosis via ligation of Fas. Moreover, although activated CD8 cells that express Fas ligand and Fas eliminate CD4 cells through a Fas-dependent mechanism, they are themselves resistant to Fas-dependent apoptosis. These findings indicate a fundamental difference between the two major T cell subsets with regard to sensitivity to Fas-dependent apoptosis, expression of Fas ligand, and mediation of suppressive activity following immunization with superantigen.
通过TCR刺激成熟的CD4细胞会诱导细胞活化和扩增,随后通常会通过一种称为活化诱导细胞死亡的凋亡形式进行克隆清除。一般认为,CD4细胞凋亡的这一过程反映了克隆自杀,且独立于其他细胞类型。在此我们表明,在对超抗原葡萄球菌肠毒素A的应答过程中,活化的CD8细胞而非活化的CD4细胞会抑制CD4细胞的增殖反应。CD8细胞的抑制作用反映了它们通过Fas连接诱导CD4细胞凋亡的能力。此外,虽然表达Fas配体和Fas的活化CD8细胞通过Fas依赖机制清除CD4细胞,但它们自身对Fas依赖的凋亡具有抗性。这些发现表明,在对超抗原免疫后,两个主要T细胞亚群在对Fas依赖凋亡的敏感性、Fas配体的表达以及抑制活性的介导方面存在根本差异。