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用于抗 LILRB4 CAR-T 细胞的开关蛋白适配器

英文原题:A Switch Protein Adapter for Anti-LILRB4 CAR-T Cells.

查看英文原题

A Switch Protein Adapter for Anti-LILRB4 CAR-T Cells.

PubMed 2024/12/11(内容时间) Eur J Immunol Q2 · IF 4.1(JCR 2025)

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中文摘要

CAR-T 免疫疗法治疗某些血液系统恶性肿瘤已显示出显著疗效。利用具有临床应用前景的CAR-T 细胞并联合适配蛋白进行重定向,可能成为靶向其他血液系统和实体瘤的有效策略。我们建立了一种基于融合抗体的灵活策略,可联合新型抗白细胞免疫球蛋白样受体B4(LILRB4)CAR-T 细胞靶向多种肿瘤类型。具体而言,我们工程化设计了转换蛋白(SwP)适配器,将LILRB4胞外结构域分别与抗CD19或抗CD20单链可变片段(scFv)融合。这些SwP可在体外和体内充分刺激抗LILRB4 CAR-T 细胞,靶向表达SwP标签的LILRB4-CD19+及LILRB4-CD20+癌症。该策略有望使CAR-T 细胞重定向至多种肿瘤抗原和癌症类型,成为扩大细胞免疫治疗影响范围的有价值方法。

展开英文摘要原文

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.

论文信息

作者
Huang R、Chen H、Xie J、Lou Q、Tan L、Zhang N、An Z、John S
单位
Department of Physiology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.United States
期刊
European journal of immunology2025 Feb
原文标识
PubMed 39663681 · DOI 10.1002/eji.202451172