Jung G, Honsik C J, Reisfeld R A, Müller-Eberhard H J
Proc Natl Acad Sci U S A. 1986 Jun;83(12):4479-83. doi: 10.1073/pnas.83.12.4479.
Cytotoxic T-cell clones have been shown to be capable of killing unrelated target cells in the presence of heteroconjugates consisting of OKT3 (monoclonal antibody against cell surface antigen T3) and targeting antibody. In contrast, human peripheral blood T cells were not known to have this ability, although these cells have been shown to undergo proliferation in response to OKT3 and accessory signals. Here we report that OKT3-stimulated human peripheral blood mononuclear cells effectively killed human melanoma or Raji cells coated with anti-target-cell--OKT3 conjugates. The extent of target-cell killing by stimulated effector cells was much greater than that observed with unstimulated cells, in spite of down-regulation of the T3 structure on the OKT3-treated cells. Target-cell lysis occurred at physiological concentrations of effector cells and was inhibited by monomeric OKT3, indicating that killing was T-cell-mediated.
细胞毒性T细胞克隆已被证明在由OKT3(抗细胞表面抗原T3的单克隆抗体)和靶向抗体组成的异源缀合物存在的情况下,能够杀死不相关的靶细胞。相比之下,尽管已证明人类外周血T细胞在响应OKT3和辅助信号时会发生增殖,但它们并不具有这种能力。在此我们报告,OKT3刺激的人类外周血单个核细胞能有效杀死包被有抗靶细胞-OKT3缀合物的人类黑色素瘤细胞或Raji细胞。尽管经OKT3处理的细胞上T3结构下调,但受刺激的效应细胞对靶细胞的杀伤程度远大于未受刺激的细胞。靶细胞裂解在效应细胞的生理浓度下发生,并被单体OKT3抑制,表明杀伤是由T细胞介导的。