Adoptive immunotherapy for acute non-lymphocytic leukaemia: a long-term follow up.

J F Denegri, J W Thomas
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引用次数: 3

Abstract

Immune cells cultured in vitro against autologous blast cells were infused twice in 8 patients with ANLL after achieving complete remission. 3 of the 8 patients remained in first remission for 74-94 months and they appeared to be cured of their leukaemia. These 3 patients received significantly higher numbers of in vitro sensitized immune cells as well as having a better recovery of the in vitro cultured cells. The other 5 patients relapsed within a year of diagnosis; 3 of them had had organomegaly and a preceding myeloproliferative disorder at diagnosis. None of 20 ANLL patients in complete remission treated simultaneously with similar chemotherapy at our institution remained in first complete remission, nor were long-term survivors. Adoptive immunotherapy with in vitro sensitized immune cells may be effective treatment in acute leukaemia. The therapeutic potential of infusion of in vitro stimulated autologous immune cells requires further investigation.

急性非淋巴细胞白血病的过继免疫治疗:长期随访。
8例ANLL患者在完全缓解后,用体外培养的抗自体母细胞的免疫细胞输注两次。8例患者中有3例在首次缓解期保持了74-94个月,他们的白血病似乎已经治愈。这3例患者的体外致敏免疫细胞数量明显增加,体外培养细胞的恢复也较好。其余5例在确诊后1年内复发;其中3例在诊断时有器官肿大和先前的骨髓增生性疾病。在我们机构同时接受类似化疗的20例完全缓解的ANLL患者中,没有一个保持首次完全缓解,也没有长期幸存者。体外致敏免疫细胞过继免疫治疗可能是急性白血病的有效治疗方法。输注体外刺激的自体免疫细胞的治疗潜力有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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