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非清髓性预处理后,移植经基因改造的 HLA 匹配外周血祖细胞用于获得性免疫缺陷综合征患者的血液系统恶性肿瘤治疗。

Nonmyeloablative conditioning followed by transplantation of genetically modified HLA-matched peripheral blood progenitor cells for hematologic malignancies in patients with acquired immunodeficiency syndrome.

作者信息

Kang Elizabeth M, de Witte Moniek, Malech Harry, Morgan Richard A, Phang Sheila, Carter Charles, Leitman Susan F, Childs Richard, Barrett A John, Little Richard, Tisdale John F

机构信息

Molecular and Clinical Hematology Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Blood. 2002 Jan 15;99(2):698-701. doi: 10.1182/blood.v99.2.698.

Abstract

To assess the safety and efficacy of nonmyeloablative allogeneic transplantation in patients with HIV infection, a clinical protocol was initiated in patients with refractory hematologic malignancies and concomitant HIV infection. The results from the first 2 patients are reported. The indications for transplantation were treatment-related acute myelogenous leukemia and primary refractory Hodgkin disease in patients 1 and 2, respectively. Only patient 1 received genetically modified cells. Both patients tolerated the procedure well with minimal toxicity, and complete remissions were achieved in both patients, but patient 2 died of relapsed Hodgkin disease 12 months after transplantation. Patient 1 continues in complete remission with undetectable HIV levels and rising CD4 counts, and with both the therapeutic and control gene transfer vectors remaining detectable at low levels more than 2 years after transplantation. These results suggest that nonmyeloablative allogeneic transplantation in the context of highly active antiretroviral therapy is feasible in patients with treatment-sensitive HIV infection.

摘要

为评估非清髓性异基因移植治疗HIV感染患者的安全性和有效性,针对难治性血液系统恶性肿瘤合并HIV感染患者启动了一项临床方案。报告了前2例患者的结果。患者1和患者2的移植指征分别为治疗相关急性髓性白血病和原发性难治性霍奇金病。仅患者1接受了基因改造细胞。两名患者对该程序耐受性良好,毒性极小,均实现完全缓解,但患者2在移植后12个月死于复发性霍奇金病。患者1持续完全缓解,HIV水平检测不到,CD4计数上升,移植后2年多治疗性和对照基因转移载体均仍可在低水平检测到。这些结果表明,在高效抗逆转录病毒治疗背景下,非清髓性异基因移植对于治疗敏感的HIV感染患者是可行的。

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