Department of Medicine, Division of Hematology and Oncology, David Geffen School of Medicine at University of California, Los Angeles, Los Angeles, California, United States of America.
Stem Cell and Gene Therapy Program, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
PLoS Pathog. 2017 Dec 28;13(12):e1006753. doi: 10.1371/journal.ppat.1006753. eCollection 2017 Dec.
Chimeric Antigen Receptor (CAR) T-cells have emerged as a powerful immunotherapy for various forms of cancer and show promise in treating HIV-1 infection. However, significant limitations are persistence and whether peripheral T cell-based products can respond to malignant or infected cells that may reappear months or years after treatment remains unclear. Hematopoietic Stem/Progenitor Cells (HSPCs) are capable of long-term engraftment and have the potential to overcome these limitations. Here, we report the use of a protective CD4 chimeric antigen receptor (C46CD4CAR) to redirect HSPC-derived T-cells against simian/human immunodeficiency virus (SHIV) infection in pigtail macaques. CAR-containing cells persisted for more than 2 years without any measurable toxicity and were capable of multilineage engraftment. Combination antiretroviral therapy (cART) treatment followed by cART withdrawal resulted in lower viral rebound in CAR animals relative to controls, and demonstrated an immune memory-like response. We found CAR-expressing cells in multiple lymphoid tissues, decreased tissue-associated SHIV RNA levels, and substantially higher CD4/CD8 ratios in the gut as compared to controls. These results show that HSPC-derived CAR T-cells are capable of long-term engraftment and immune surveillance. This study demonstrates for the first time the safety and feasibility of HSPC-based CAR therapy in a large animal preclinical model.
嵌合抗原受体 (CAR) T 细胞已成为治疗各种癌症的一种强大的免疫疗法,并在治疗 HIV-1 感染方面显示出前景。然而,其存在持久性的显著限制,并且外周 T 细胞为基础的产品是否能够对恶性或感染细胞做出反应,这些细胞可能在治疗后数月或数年后再次出现,目前尚不清楚。造血干细胞/祖细胞 (HSPCs) 能够长期植入,并有可能克服这些限制。在这里,我们报告了使用保护性 CD4 嵌合抗原受体 (C46CD4CAR) 来重新定向 HSPC 衍生的 T 细胞以抵抗恒河猴/人免疫缺陷病毒 (SHIV) 感染。携带 CAR 的细胞持续存在超过 2 年,没有任何可测量的毒性,并且能够进行多谱系植入。联合抗逆转录病毒治疗 (cART) 治疗后再停药,与对照组相比,CAR 动物的病毒反弹较低,并表现出免疫记忆样反应。我们在多个淋巴组织中发现了表达 CAR 的细胞,与对照组相比,组织相关的 SHIV RNA 水平降低,并且肠道中的 CD4/CD8 比值显著升高。这些结果表明,HSPC 衍生的 CAR T 细胞能够长期植入和免疫监视。这项研究首次证明了基于 HSPC 的 CAR 疗法在大型动物临床前模型中的安全性和可行性。