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

被引:61
作者
Kang, EM
de Witte, M
Malech, H
Morgan, RA
Phang, S
Carter, C
Leitman, SF
Childs, R
Barrett, AJ
Little, R
Tisdale, JF
机构
[1] NIDDKD, Mol & Clin Hematol Branch, NIH, Bethesda, MD 20892 USA
[2] NIAID, NIH, Bethesda, MD 20892 USA
[3] NHGRI, NIH, Bethesda, MD 20892 USA
[4] NIH, Dept Nursing, Ctr Clin, Bethesda, MD 20892 USA
[5] NIH, Dept Transfus Med, Ctr Clin, Bethesda, MD 20892 USA
[6] NHLBI, NIH, Bethesda, MD 20892 USA
[7] NCI, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1182/blood.V99.2.698
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. (Blood. 2002;99:698-701) (C) 2002 by The American Society of Hematology.
引用
收藏
页码:698 / 701
页数:4
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