Kaplan J H, Lee L S, Lockwood S H
Immunol Lett. 1982 May;4(5):269-73. doi: 10.1016/0165-2478(82)90050-5.
Two major T-cell subpopulations obtained from human peripheral blood were studied their capacity to be activated by the tumor promoting agent, 12-O-tetradecanoylphorbol-13-acetate (TPA). The subpopulations were identified and separated from each other by their reactivity either to the monoclonal antibody, OKT4 or OKT8, followed by complement-dependent lysis. The fraction enriched in T8+ cells showed approximately a 1.2-2.0-fold greater proliferative response to TPA (20 ng/ml) than did the T4+ cell subset. Optimal activation required the presence of monocytes. Comparison of the mitotic activity showed that the sum of each T-cell subset was less than a mixture of the two. This indicates either a unilateral or cooperative interaction of mitogenesis in the presence of TPA.
对从人外周血中获得的两个主要T细胞亚群进行了研究,观察它们被肿瘤促进剂12-O-十四烷酰佛波醇-13-乙酸酯(TPA)激活的能力。通过它们对单克隆抗体OKT4或OKT8的反应性,随后进行补体依赖性裂解,对这些亚群进行鉴定并彼此分离。富含T8+细胞的部分对TPA(20 ng/ml)的增殖反应比T4+细胞亚群大约高1.2至2.0倍。最佳激活需要单核细胞的存在。有丝分裂活性的比较表明,每个T细胞亚群的总和小于两者的混合物。这表明在TPA存在下有丝分裂的单向或协同相互作用。