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嵌合抗原受体(CAR)与药物:增强 CAR-T 细胞疗法的药理学途径。

CARs and Drugs: Pharmacological Ways of Boosting CAR-T-Cell Therapy.

机构信息

Department of Hematology and Internal Oncology, University Hospital Regensburg, 93053 Regensburg, Germany.

Department of Dermatology, Friedrich-Alexander-Universität Erlangen-Nürnberg, Universitätsklinikum Erlangen, Hartmannstraße 14, 91052 Erlangen, Germany.

出版信息

Int J Mol Sci. 2023 Jan 25;24(3):2342. doi: 10.3390/ijms24032342.

Abstract

The development of chimeric antigen receptor T cells (CAR-T cells) has marked a new era in cancer immunotherapy. Based on a multitude of durable complete remissions in patients with hematological malignancies, FDA and EMA approval was issued to several CAR products targeting lymphoid leukemias and lymphomas. Nevertheless, about 50% of patients treated with these approved CAR products experience relapse or refractory disease necessitating salvage strategies. Moreover, in the vast majority of patients suffering from solid tumors, CAR-T-cell infusions could not induce durable complete remissions so far. Crucial obstacles to CAR-T-cell therapy resulting in a priori CAR-T-cell refractory disease or relapse after initially successful CAR-T-cell therapy encompass antigen shutdown and CAR-T-cell dysfunctionality. Antigen shutdown predominately rationalizes disease relapse in hematological malignancies, and CAR-T-cell dysfunctionality is characterized by insufficient CAR-T-cell proliferation and cytotoxicity frequently observed in patients with solid tumors. Thus, strategies to surmount those obstacles are being developed with high urgency. In this review, we want to highlight different approaches to combine CAR-T cells with drugs, such as small molecules and antibodies, to pharmacologically boost CAR-T-cell therapy. In particular, we discuss how certain drugs may help to counteract antigen shutdown and CAR-T-cell dysfunctionality in both hematological malignancies and solid tumors.

摘要

嵌合抗原受体 T 细胞(CAR-T 细胞)的发展标志着癌症免疫治疗的新时代。基于血液恶性肿瘤患者的许多持久完全缓解,FDA 和 EMA 批准了几种针对淋巴白血病和淋巴瘤的 CAR 产品。然而,约 50%接受这些批准的 CAR 产品治疗的患者出现复发或难治性疾病,需要挽救策略。此外,在绝大多数患有实体瘤的患者中,CAR-T 细胞输注迄今为止未能诱导持久的完全缓解。导致 CAR-T 细胞治疗的关键障碍,导致最初成功的 CAR-T 细胞治疗后出现预先 CAR-T 细胞难治性疾病或复发,包括抗原失活和 CAR-T 细胞功能障碍。抗原失活主要使血液恶性肿瘤中的疾病复发合理化,而 CAR-T 细胞功能障碍的特征是在实体瘤患者中经常观察到的 CAR-T 细胞增殖和细胞毒性不足。因此,正在以高度的紧迫感开发克服这些障碍的策略。在这篇综述中,我们想强调将 CAR-T 细胞与药物(如小分子和抗体)结合使用的不同方法,以药理学增强 CAR-T 细胞治疗。特别是,我们讨论了某些药物如何有助于对抗血液恶性肿瘤和实体肿瘤中的抗原失活和 CAR-T 细胞功能障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d05/9916546/3b78047d7289/ijms-24-02342-g001.jpg

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