造血细胞移植治疗HIV感染的进展。

IF 1.7 Q4 CELL BIOLOGY
Stem Cells and Cloning-Advances and Applications Pub Date : 2015-07-28 eCollection Date: 2015-01-01 DOI:10.2147/SCCAA.S56050
Lawrence D Petz, John C Burnett, Haitang Li, Shirley Li, Richard Tonai, Milena Bakalinskaya, Elizabeth J Shpall, Sue Armitage, Joanne Kurtzberg, Donna M Regan, Pamela Clark, Sergio Querol, Jonathan A Gutman, Stephen R Spellman, Loren Gragert, John J Rossi
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引用次数: 13

摘要

根据世界卫生组织2014年的估计,全球有超过3500万人感染了HIV-1。对于那些获得抗逆转录病毒治疗的人来说,这些药物可以有效地抑制,但不能治愈HIV-1感染。事实上,唯一记录在案的HIV/AIDS治愈病例是一名患有HIV-1和急性髓性白血病的患者,他接受了同种异体造血细胞移植(HCT),其移植物携带了抗HIV的CCR5-∆32/∆32突变。在艾滋病毒1型和恶性肿瘤患者中使用HCT治疗艾滋病毒/艾滋病的其他尝试取得了好坏参半的结果,因为在少数病例中,令人鼓舞的病毒根除证据被潜在癌症或其他并发症导致的不良临床结果所抵消。这种临床策略依赖于抗hiv的造血干细胞和祖细胞,这些细胞含有天然的CCR5-∆32/∆32突变,或经过基因改造以抵抗hiv。然而,抗艾滋病毒脐带血的HCT仍然是一个很有希望的选择,特别是含有CCR5-∆32/∆32单位的脐带血或基因修饰的人类白细胞抗原匹配脐带血。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Progress toward curing HIV infection with hematopoietic cell transplantation.

HIV-1 infection afflicts more than 35 million people worldwide, according to 2014 estimates from the World Health Organization. For those individuals who have access to antiretroviral therapy, these drugs can effectively suppress, but not cure, HIV-1 infection. Indeed, the only documented case for an HIV/AIDS cure was a patient with HIV-1 and acute myeloid leukemia who received allogeneic hematopoietic cell transplantation (HCT) from a graft that carried the HIV-resistant CCR5-∆32/∆32 mutation. Other attempts to establish a cure for HIV/AIDS using HCT in patients with HIV-1 and malignancy have yielded mixed results, as encouraging evidence for virus eradication in a few cases has been offset by poor clinical outcomes due to the underlying cancer or other complications. Such clinical strategies have relied on HIV-resistant hematopoietic stem and progenitor cells that harbor the natural CCR5-∆32/∆32 mutation or that have been genetically modified for HIV-resistance. Nevertheless, HCT with HIV-resistant cord blood remains a promising option, particularly with inventories of CCR5-∆32/∆32 units or with genetically modified, human leukocyte antigen-matched cord blood.

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来源期刊
CiteScore
6.50
自引率
0.00%
发文量
10
审稿时长
16 weeks
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