Laboratoire de Biochimie et Thérapies Moléculaires, Faculté de Pharmacie, Université Saint Joseph de Beyrouth, Beirut, Lebanon.
Université de Paris, CNRS, INSERM, UTCBS, Unité des technologies Chimiques et Biologiques pour la Santé, Paris, France.
Front Immunol. 2022 Feb 8;13:830292. doi: 10.3389/fimmu.2022.830292. eCollection 2022.
During this last decade, adoptive transfer of T lymphocytes genetically modified to express chimeric antigen receptors (CARs) emerged as a valuable therapeutic strategy in hematological cancers. However, this immunotherapy has demonstrated limited efficacy in solid tumors. The main obstacle encountered by CAR-T cells in solid malignancies is the immunosuppressive tumor microenvironment (TME). The TME impedes tumor trafficking and penetration of T lymphocytes and installs an immunosuppressive milieu by producing suppressive soluble factors and by overexpressing negative immune checkpoints. In order to overcome these hurdles, new CAR-T cells engineering strategies were designed, to potentiate tumor recognition and infiltration and anti-cancer activity in the hostile TME. In this review, we provide an overview of the major mechanisms used by tumor cells to evade immune defenses and we critically expose the most optimistic engineering strategies to make CAR-T cell therapy a solid option for solid tumors.
在过去的十年中,过继转导表达嵌合抗原受体(CAR)的 T 淋巴细胞已成为血液系统恶性肿瘤的一种有价值的治疗策略。然而,这种免疫疗法在实体瘤中的疗效有限。CAR-T 细胞在实体恶性肿瘤中遇到的主要障碍是免疫抑制性肿瘤微环境(TME)。TME 通过产生抑制性可溶性因子和过度表达负性免疫检查点来阻碍 T 淋巴细胞的肿瘤运输和浸润,并建立免疫抑制环境。为了克服这些障碍,设计了新的 CAR-T 细胞工程策略,以增强肿瘤识别和浸润以及在恶劣的 TME 中的抗癌活性。在这篇综述中,我们概述了肿瘤细胞逃避免疫防御的主要机制,并批判性地揭示了最有希望的工程策略,以使 CAR-T 细胞疗法成为实体瘤的一种可靠选择。