抗lilrb4 CAR-T细胞的开关蛋白适配器

IF 4.5 3区 医学 Q2 IMMUNOLOGY
Ryan Huang, Heyu Chen, Jingjing Xie, Qi Lou, Lingxiao Tan, Ningyan Zhang, Zhiqiang An, Samuel John, Cheng Cheng Zhang
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引用次数: 0

摘要

嵌合抗原受体- t细胞(CAR-T)免疫疗法在治疗某些血液系统恶性肿瘤方面显示出显著的效果。利用临床相关CAR-T细胞与适配蛋白结合的重定向策略可能是针对其他血液学和实体癌症的有效策略。我们建立了一种基于融合抗体的策略,可以灵活地靶向多种肿瘤类型,并结合一种新的抗白细胞免疫球蛋白样受体- b4 (LILRB4) CAR-T细胞。具体来说,我们设计了包含LILRB4细胞外结构域的开关蛋白(SwP)适配器,该适配器与抗cd19或抗cd20单链可变片段(scFv)融合。这些SwPs足以刺激抗lilrb4 CAR-T细胞在体外和体内对抗swp标记的LILRB4-CD19+和LILRB4-CD20+癌症。这一策略可能允许CAR-T细胞被重定向对抗多种肿瘤抗原和癌症类型,并成为扩大细胞免疫治疗影响的一种有价值的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Switch Protein Adapter for Anti-LILRB4 CAR-T Cells.

Chimeric antigen receptor-T cell (CAR-T) immunotherapy has shown remarkable results for the treatment of certain hematologic malignancies. A redirection strategy that utilizes clinically relevant CAR-T cells in combination with adapter proteins may be an effective strategy to target other hematologic and solid cancers. We established a fusion antibody-based strategy with flexibility to target multiple tumor types in combination with a novel anti-leukocyte immunoglobulin-like receptor-B 4 (LILRB4) CAR-T cell. Specifically, we engineered switch protein (SwP) adapters containing the LILRB4 extracellular domain fused to either an anti-CD19 or anti-CD20 single-chain variable fragment (scFv). These SwPs were sufficient to stimulate anti-LILRB4 CAR-T cells against SwP-tagged LILRB4-CD19+ and LILRB4-CD20+ cancers in vitro and in vivo. This strategy may allow CAR-T cells to be redirected against a variety of tumor antigens and cancer types and become a valuable approach to expand the impact of cellular immunotherapy.

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来源期刊
CiteScore
8.30
自引率
3.70%
发文量
224
审稿时长
2 months
期刊介绍: The European Journal of Immunology (EJI) is an official journal of EFIS. Established in 1971, EJI continues to serve the needs of the global immunology community covering basic, translational and clinical research, ranging from adaptive and innate immunity through to vaccines and immunotherapy, cancer, autoimmunity, allergy and more. Mechanistic insights and thought-provoking immunological findings are of interest, as are studies using the latest omics technologies. We offer fast track review for competitive situations, including recently scooped papers, format free submission, transparent and fair peer review and more as detailed in our policies.
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