Suraiya Anisha B, Evtimov Vera J, Truong Vinh X, Boyd Richard L, Forsythe John S, Boyd Nicholas R
Department of Materials Science and Engineering, Monash Institute of Medical Engineering, Monash University, Clayton, Victoria 3800, Australia; Cartherics Pty, Ltd., Clayton, Victoria 3168, Australia.
Cartherics Pty, Ltd., Clayton, Victoria 3168, Australia.
Transl Oncol. 2022 Oct;24:101477. doi: 10.1016/j.tranon.2022.101477. Epub 2022 Jul 26.
Chimeric antigen receptor (CAR-) T cells are revolutionizing cancer treatment, as a direct result of their clinical impact on the treatment of hematological malignancies. However for solid tumors, CAR-T cell therapeutic efficacy remains limited, primarily due to the complex immunosuppressive tumor microenvironment, inefficient access to tumor cells and poor persistence of the killer cells. In this in vitro study, an injectable, gelatin-based micro-hydrogel system that can encapsulate and deliver effective CAR-T therapy is investigated. CAR-T cells targeting TAG-72, encapsulated in these microgels possessed high viability (> 87%) after 7 days, equivalent to those grown under normal expansion conditions, with retention of the T cell phenotype and functionality. Microgel recovered CAR-T cells demonstrated potent on-target cytotoxicity against human ovarian cancer in vitro and on three-dimensional tumor spheroids, by completely eliminating tumor cells. The gelatin-based micro-hydrogels have the potential to serve as carrier systems to augment CAR-T immunotherapeutic treatment of solid tumors.
嵌合抗原受体(CAR)-T细胞正在彻底改变癌症治疗,这是其对血液系统恶性肿瘤治疗产生临床影响的直接结果。然而,对于实体瘤,CAR-T细胞的治疗效果仍然有限,主要是由于复杂的免疫抑制肿瘤微环境、难以有效接触肿瘤细胞以及杀伤细胞的持久性较差。在这项体外研究中,研究了一种可注射的、基于明胶的微水凝胶系统,该系统能够封装并提供有效的CAR-T治疗。封装在这些微凝胶中的靶向TAG-72的CAR-T细胞在7天后具有较高的活力(>87%),与在正常扩增条件下生长的细胞相当,同时保留了T细胞表型和功能。微凝胶回收的CAR-T细胞在体外对人卵巢癌以及在三维肿瘤球体上表现出强大的靶向细胞毒性,能够完全消除肿瘤细胞。基于明胶的微水凝胶有潜力作为载体系统,增强对实体瘤的CAR-T免疫治疗。