Fleischer B
Nature. 1984;308(5957):365-7. doi: 10.1038/308365a0.
Mature human T lymphocytes can be separated by monoclonal antibodies OKT4 and OKT8 according to their surface phenotypes into T4+T8- and T4-T8+ subsets. From short-term experiments using bulk cultures, the helper/inducer function has been assigned to the T4+T8- subset and the cytotoxic/suppressor function to the T4-T8+ subset. Thus if T lymphocytes are separated after stimulation in a mixed lymphocyte reaction (MLR), the entire cytotoxic activity is found in the T4-T8+ fraction whereas the T4+T8- fraction shows no detectable cytotoxicity. If, however, T lymphocytes are cloned after MLR and grown in long-term culture, a surprisingly large fraction of T4+ T lymphocyte clones (TLC) shows cytotoxic activity. Here we report that T4+ TLC can acquire specific cytotoxicity during in vitro cultivation.
成熟的人类T淋巴细胞可通过单克隆抗体OKT4和OKT8,根据其表面表型分为T4+T8-和T4-T8+亚群。通过使用大量培养物的短期实验,辅助/诱导功能已被确定为T4+T8-亚群,而细胞毒性/抑制功能则为T4-T8+亚群。因此,如果在混合淋巴细胞反应(MLR)中刺激后分离T淋巴细胞,全部细胞毒性活性存在于T4-T8+部分,而T4+T8-部分则未显示可检测到的细胞毒性。然而,如果在MLR后克隆T淋巴细胞并在长期培养中生长,相当大比例的T4+ T淋巴细胞克隆(TLC)显示出细胞毒性活性。在此我们报告,T4+ TLC在体外培养期间可获得特异性细胞毒性。