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靶向 TRBC1 的抗体药物偶联物用于治疗 T 细胞肿瘤

英文原题:TRBC1-targeting antibody-drug conjugates for the treatment of T cell cancers.

查看英文原题

TRBC1-targeting antibody-drug conjugates for the treatment of T cell cancers.

PubMed 2024/03/27(内容时间) Nature Q1 · IF 56.1(JCR 2025)

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中文摘要

抗体和嵌合抗原受体(CAR)T细胞介导的靶向治疗改善了实体瘤和血液系统恶性肿瘤患者的生存1-9。患有T细胞白血病和淋巴瘤(统称为T细胞癌症)的成人存活期短10,11,且缺乏此类靶向治疗。

因此,T细胞癌症尤其需要开发CAR-T 细胞和抗体以改善患者预后。临床前研究表明,靶向T细胞受体β链恒定区1(TRBC1)可杀死癌性T细胞,同时保留足够的健康T细胞以维持免疫12,使TRBC1成为治疗T细胞癌症的有吸引力的靶点。

然而,抗TRBC1 CAR-T 细胞的首次人体临床试验报告了低缓解率和抗TRBC1 CAR-T 细胞的不明原因丢失13,14。

在此,我们证明CAR-T 细胞因被患者正常T细胞杀死而丢失,从而降低其疗效。为规避这一问题,我们开发了一种抗体-药物偶联物,可在体外杀死TRBC1+癌细胞,并在小鼠模型中治愈人类T细胞癌症。抗TRBC1抗体-药物偶联物可能为TRBC1靶向提供最佳形式,并在T细胞癌症患者中产生优越的缓解。

展开英文摘要原文

Antibody and chimeric antigen receptor (CAR) T cell-mediated targeted therapies have improved survival in patients with solid and haematologic malignancies 1-9 . Adults with T cell leukaemias and lymphomas, collectively called T cell cancers, have short survival 10,11 and lack such targeted therapies.

Thus, T cell cancers particularly warrant the development of CAR T cells and antibodies to improve patient outcomes. Preclinical studies showed that targeting T cell receptor -chain constant region 1 (TRBC1) can kill cancerous T cells while preserving sufficient healthy T cells to maintain immunity 12 , making TRBC1 an attractive target to treat T cell cancers.

However, the first-in-human clinical trial of anti-TRBC1 CAR T cells reported a low response rate and unexplained loss of anti-TRBC1 CAR T cells 13,14 .

Here we demonstrate that CAR T cells are lost due to killing by the patient's normal T cells, reducing their efficacy. To circumvent this issue, we developed an antibody-drug conjugate that could kill TRBC1 + cancer cells in vitro and cure human T cell cancers in mouse models. The anti-TRBC1 antibody-drug conjugate may provide an optimal format for TRBC1 targeting and produce superior responses in patients with T cell cancers.

论文信息

作者
Nichakawade TD、Ge J、Mog BJ、Lee BS、Pearlman AH、Hwang MS、DiNapoli SR、Wyhs N
第一作者单位
Ludwig Center and Lustgarten Laboratory, Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.United States
通讯作者单位
Ludwig Center and Lustgarten Laboratory, Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Baltimore, MD, USA. spaul19@jhmi.edu.United States
文献类型
美国 NIH 资助研究
期刊
Nature2024 Apr
原文标识
PubMed 38538786 · DOI 10.1038/s41586-024-07233-2