Mitsuya H, Matis L A, Megson M, Cohen O J, Mann D L, Gallo R C, Broder S
Lancet. 1984 Mar 24;1(8378):649-52. doi: 10.1016/s0140-6736(84)92169-x.
Six patients with malignant disorders associated with human T-cell leukaemia/lymphoma virus (HTLV) were studied to see whether long-term cultures of immune T cells reactive against HTLV-infected tumour cells could be achieved. Immune T-cell lines could not be developed from the cells of five patients who died or eventually had a relapse of disease, but in one patient who had an unusually long remission of his disease after therapy, immune T-cell lines were propagated that could produce their own T-cell growth factor and proliferate upon stimulation with autologous tumour cells and also specifically lyse HTLV-infected target cells. These immune T cells recognised the presence of circulating HTLV-bearing neoplastic cells in another patient with HTLV-associated T-cell leukaemia, who had been in clinical remission after chemotherapy when this study started, thereby providing early evidence of relapse.
对6例与人类T细胞白血病/淋巴瘤病毒(HTLV)相关的恶性疾病患者进行了研究,以观察是否能够实现针对HTLV感染肿瘤细胞的免疫T细胞的长期培养。从5例死亡或最终疾病复发的患者细胞中未能培养出免疫T细胞系,但在1例经治疗后疾病缓解期异常长的患者中,培养出了能够产生自身T细胞生长因子并在自体肿瘤细胞刺激下增殖、还能特异性裂解HTLV感染靶细胞的免疫T细胞系。这些免疫T细胞识别出另一例HTLV相关T细胞白血病患者循环中携带HTLV的肿瘤细胞的存在,该患者在本研究开始时化疗后处于临床缓解期,从而为复发提供了早期证据。