用光增强 CAR T 细胞功能。

IF 8.1 1区 医学 Q1 IMMUNOLOGY
Winson Cai, Kento Tanaka, Xiaoli Mi, Vinagolu K Rajasekhar, Jonathan F Khan, Sarah Yoo, Elisa de Stanchina, Jahan Rahman, Serena Mathew, Parwiz Abrahimi, Sydney Souness, Terence J Purdon, James R McDowell, Jeremy Meyerberg, Takeshi Fujino, John H Healey, Omar Abdel-Wahab, David A Scheinberg, Renier J Brentjens, Anthony F Daniyan
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引用次数: 0

摘要

嵌合抗原受体(CAR)T 细胞疗法在治疗 B 细胞恶性肿瘤方面取得了显著的临床成功。然而,它在实体瘤中的临床疗效却受到限制,主要原因是靶抗原异质性。为了克服抗原异质性,我们开发了过度表达LIGHT的CAR T细胞,LIGHT是癌细胞LTβR和免疫细胞HVEM的配体。表达LIGHT的CAR T细胞既表现出由CAR介导的抗原导向细胞毒性,也表现出通过LIGHT与癌细胞上的LTβR相互作用介导的抗原无关杀伤性。此外,表达LIGHT的CAR T细胞具有免疫刺激特性,能改善细胞的增殖和细胞溶解特性。这些数据表明,表达LIGHT的CAR T细胞可能是消除抗原阴性肿瘤细胞以防止抗原阴性疾病复发的一种方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Augmenting CAR T Cell Functions with LIGHT.

Chimeric antigen receptor (CAR) T-cell therapy has resulted in remarkable clinical success in the treatment of B-cell malignancies. However, its clinical efficacy in solid tumors is limited, primarily by target antigen heterogeneity. To overcome antigen heterogeneity, we developed CAR T cells that overexpress LIGHT, a ligand of both LTβR on cancer cells and HVEM on immune cells. LIGHT-expressing CAR T cells displayed both antigen-directed cytotoxicity mediated by the CAR and antigen-independent killing mediated through the interaction of LIGHT with LTβR on cancer cells. Moreover, CAR T cells expressing LIGHT had immunostimulatory properties that improved the cells' proliferation and cytolytic profile. These data indicate that LIGHT-expressing CAR T cells may provide a way to eliminate antigen-negative tumor cells to prevent antigen-negative disease relapse.

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来源期刊
Cancer immunology research
Cancer immunology research ONCOLOGY-IMMUNOLOGY
CiteScore
15.60
自引率
1.00%
发文量
260
期刊介绍: Cancer Immunology Research publishes exceptional original articles showcasing significant breakthroughs across the spectrum of cancer immunology. From fundamental inquiries into host-tumor interactions to developmental therapeutics, early translational studies, and comprehensive analyses of late-stage clinical trials, the journal provides a comprehensive view of the discipline. In addition to original research, the journal features reviews and opinion pieces of broad significance, fostering cross-disciplinary collaboration within the cancer research community. Serving as a premier resource for immunology knowledge in cancer research, the journal drives deeper insights into the host-tumor relationship, potent cancer treatments, and enhanced clinical outcomes. Key areas of interest include endogenous antitumor immunity, tumor-promoting inflammation, cancer antigens, vaccines, antibodies, cellular therapy, cytokines, immune regulation, immune suppression, immunomodulatory effects of cancer treatment, emerging technologies, and insightful clinical investigations with immunological implications.
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