Boonchalermvichian Chaiyaporn, Yan Hao, Gupta Biki, Rubin Anabel, Baker Jeanette, Negrin Robert S
Division of Blood and Marrow Transplantation and Cellular Therapy, Department of Medicine, Stanford University, Stanford, CA, United States.
Front Transplant. 2024 May 6;3:1353803. doi: 10.3389/frtra.2024.1353803. eCollection 2024.
Invariant Natural Killer T cell therapy is an emerging platform of immunotherapy for cancer treatment. This unique cell population is a promising candidate for cell therapy for cancer treatment because of its inherent cytotoxicity against CD1d positive cancers as well as its ability to induce host CD8 T cell cross priming. Substantial evidence supports that iNKT cells can modulate myelomonocytic populations in the tumor microenvironment to ameliorate immune dysregulation to antagonize tumor progression. iNKT cells can also protect from graft-versus-host disease (GVHD) through several mechanisms, including the expansion of regulatory T cells (Treg). Ultimately, iNKT cell-based therapy can retain antitumor activity while providing protection against GVHD simultaneously. Therefore, these biological properties render iNKT cells as a promising "off-the-shelf" therapy for diverse hematological malignancies and possible solid tumors. Further the introduction of a chimeric antigen recetor (CAR) can further target iNKT cells and enhance function. We foresee that improved vector design and other strategies such as combinatorial treatments with small molecules or immune checkpoint inhibitors could improve CAR iNKT persistence, functionality and leverage anti-tumor activity along with the abatement of iNKT cell dysfunction or exhaustion.
不变自然杀伤T细胞疗法是一种新兴的癌症免疫治疗平台。这种独特的细胞群体因其对CD1d阳性癌症具有内在的细胞毒性以及诱导宿主CD8 T细胞交叉启动的能力,而成为癌症细胞治疗的一个有前景的候选者。大量证据支持,不变自然杀伤T细胞可以调节肿瘤微环境中的骨髓单核细胞群体,以改善免疫失调,对抗肿瘤进展。不变自然杀伤T细胞还可以通过多种机制预防移植物抗宿主病(GVHD),包括调节性T细胞(Treg)的扩增。最终,基于不变自然杀伤T细胞的疗法可以在保留抗肿瘤活性的同时,提供对移植物抗宿主病的保护。因此,这些生物学特性使不变自然杀伤T细胞成为治疗多种血液系统恶性肿瘤和可能的实体瘤的一种有前景的“现成”疗法。此外,嵌合抗原受体(CAR)的引入可以进一步靶向不变自然杀伤T细胞并增强其功能。我们预计,改进的载体设计以及其他策略,如与小分子或免疫检查点抑制剂的联合治疗,可以提高嵌合抗原受体不变自然杀伤T细胞的持久性、功能性,并在减轻不变自然杀伤T细胞功能障碍或耗竭的同时增强抗肿瘤活性。