Iwahashi M, Tanimura H, Yamaue H, Tsunoda T, Tani M, Noguchi K, Mizobata S, Hotta T, Tamai M
Department of Gastroenterological Surgery, Wakayama Medical College, Japan.
J Clin Lab Immunol. 1993;40(1):29-37.
Autoreactive T cell clones were established from a patient with early gastric carcinoma and a healthy control in order to investigate the mechanism of suppression of autologous mixed lymphocyte reaction (AMLR) and its significance in immune surveillance against tumor. Clone 3F6 from the gastric carcinoma patient responded to only autologous non-T cells with less reactivity than 4 clones from the control subject. The proliferative response of clone 3F6 to interleukin-2 and immobilized anti-CD3 antibody was also suppressed when compared with the control clones. Autoreactive T cells were able to kill tumor cells and autologous PHA-blasts. The cytotoxic activity of clone 3F6 was also markedly suppressed when compared with the control clones. This data suggests that autoreactive T cells may be impaired in cancer patients and that this immunological disorder might cause the defective immune surveillance against tumors.
为了研究自体混合淋巴细胞反应(AMLR)的抑制机制及其在肿瘤免疫监视中的意义,从一名早期胃癌患者和一名健康对照者中建立了自身反应性T细胞克隆。来自胃癌患者的克隆3F6仅对自体非T细胞有反应,其反应性低于来自对照受试者的4个克隆。与对照克隆相比,克隆3F6对白介素-2和固定化抗CD3抗体的增殖反应也受到抑制。自身反应性T细胞能够杀伤肿瘤细胞和自体PHA-母细胞。与对照克隆相比,克隆3F6的细胞毒性活性也明显受到抑制。该数据表明癌症患者的自身反应性T细胞可能受损,这种免疫紊乱可能导致对肿瘤的免疫监视缺陷。