Deusch K, Moebius U, Meyer zum Büschenfelde K H, Meuer S C
Eur J Immunol. 1986 Nov;16(11):1433-8. doi: 10.1002/eji.1830161119.
To investigate cellular mechanisms controlling activated autoreactive T lymphocytes, a limiting dilution system was established employing cloned autoreactive major histocompatibility complex class II specific lymphocytes (a2/7) as stimulator cells for autologous peripheral blood mononuclear cells. At low responder/stimulator ratios, cytotoxic effector cells were generated capable of lysing clone a2/7. Importantly, within the population of cells mediating autocytotoxic effector function, differential specificities were found to exist. The generation of such autocytotoxic T lymphocytes appears to be inhibited by an additional population of cells circulating at lower frequency suggesting that autoreactivity is controlled at distinct levels by discrete functional cellular subsets.
为了研究控制活化的自身反应性T淋巴细胞的细胞机制,建立了一种有限稀释系统,该系统采用克隆的自身反应性主要组织相容性复合体II类特异性淋巴细胞(a2/7)作为自体外周血单个核细胞的刺激细胞。在低反应者/刺激细胞比例下,能够裂解克隆a2/7的细胞毒性效应细胞得以产生。重要的是,在介导自身细胞毒性效应功能的细胞群体中,发现存在不同的特异性。这种自身细胞毒性T淋巴细胞的产生似乎受到循环频率较低的另一细胞群体的抑制,这表明自身反应性在不同水平上由离散的功能性细胞亚群控制。