Allogeneic transplantation (allo-HCT) has led to the cure of HIV in one individual, raising the question of whether transplantation can eradicate the HIV reservoir. To test this, we here present a model of allo-HCT in SHIV-infected, cART-suppressed nonhuman primates. We infect rhesus macaques with SHIV-1157ipd3N4, suppress them with cART, then transplant them using MHC-haploidentical allogeneic donors during continuous cART. Transplant results in ~100% myeloid donor chimerism, and up to 100% T-cell chimerism. Between 9 and 47 days post-transplant, terminal analysis shows that while cell-associated SHIV DNA levels are reduced in the blood and in lymphoid organs post-transplant, the SHIV reservoir persists in multiple organs, including the brain. Sorting of donor-vs.-recipient cells reveals that this reservoir resides in recipient cells. Moreover, tetramer analysis indicates a lack of virus-specific donor immunity post-transplant during continuous cART. These results suggest that early post-transplant, allo-HCT is insufficient for recipient reservoir eradication despite high-level donor chimerism and GVHD.
Allogeneic hematopoietic cell transplantation (allo-HCT) has led to the cure of HIV in one individual, but the underlying mechanisms are unclear. Here, the authors present a model of allo-HCT in SHIV-infected nonhuman primates and show that the SHIV reservoir persists in multiple tissues early after transplantation.
同种异体移植(allo - HCT)已使一名艾滋病病毒(HIV)感染者被治愈,这引发了移植是否能根除HIV储存库的问题。为了验证这一点,我们在此展示了一个在感染猴免疫缺陷病毒(SHIV)且接受抗逆转录病毒疗法(cART)抑制的非人灵长类动物中进行同种异体移植的模型。我们用SHIV - 1157ipd3N4感染恒河猴,用cART对其进行抑制,然后在持续cART治疗期间使用主要组织相容性复合体(MHC)半相合的同种异体供体对它们进行移植。移植导致约100%的髓系供体细胞嵌合,以及高达100%的T细胞嵌合。在移植后的9到47天之间,终末分析显示,虽然移植后血液和淋巴器官中细胞相关的SHIV DNA水平降低,但SHIV储存库在包括大脑在内的多个器官中持续存在。对供体细胞和受体细胞进行分选显示,该储存库存在于受体细胞中。此外,四聚体分析表明,在持续cART治疗期间,移植后缺乏病毒特异性的供体免疫。这些结果表明,在移植后的早期,尽管存在高水平的供体细胞嵌合和移植物抗宿主病(GVHD),同种异体移植仍不足以根除受体的储存库。
同种异体造血细胞移植(allo - HCT)已使一名HIV感染者被治愈,但其潜在机制尚不清楚。在此,作者展示了一个在感染SHIV的非人灵长类动物中进行同种异体移植的模型,并表明在移植后的早期,SHIV储存库在多个组织中持续存在。