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拓宽视野:CAR-T 细胞在当前适应证之外的潜在应用

英文原题:Broadening the horizon: potential applications of CAR-T cells beyond current indications.

PubMed 2023/11/27(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

研究概要

自 CAR-T 细胞疗法在 B-ALL 中首次取得巨大成功以来,通过工程化改造免疫细胞来治疗血液系统恶性肿瘤一直是研究的重点。

中文摘要

自B-ALL中CAR-T细胞疗法首次取得显著成功以来,工程化免疫细胞治疗血液系统恶性肿瘤一直是研究重点。如今,多种疾病即使处于高度治疗耐药或复发状态也可接受治疗。目前,若干CD19或BCMA特异性CAR-T细胞疗法已获批用于急性淋巴细胞白血病(ALL)、弥漫大B细胞淋巴瘤(DLBCL)、套细胞淋巴瘤(MCL)、多发性骨髓瘤(MM)和滤泡性淋巴瘤(FL)。即使在既往预后极差的病例中,这些疗法的实施也显著改善了患者结局和生存。本综述全面介绍一组选定血液系统恶性肿瘤中CAR-T细胞疗法的研究现状、近期创新和应用,聚焦B细胞及T细胞恶性肿瘤,包括皮肤T细胞淋巴瘤和外周T细胞淋巴瘤(T-ALL、PTCL、CTCL)、急性髓系白血病(AML)、慢性髓系白血病(CML)、慢性淋巴细胞白血病(CLL)、经典型霍奇金淋巴瘤(HL)、伯基特淋巴瘤(BL)、毛细胞白血病(HCL)和华氏巨球蛋白血症(WM)。这些疾病高度异质;我们重点介绍若干反复采用的方法(与现有疗法联合、清除健康细胞上的靶点)、多种疾病共用的靶点(CD30、CD38、TRBC1/2),以及需要个体化方案的独特特征。此外,我们关注各类疾病和亚型中CAR-T疗法当前的局限,例如免疫抑制性肿瘤微环境(TME)、靶向肿瘤外组织风险及不良事件发生情况的差异。最后,我们展望CAR-T工程领域的新创新,如人工智能的应用,以及CAR-T细胞在日常临床治疗方案中的未来作用。

展开英文摘要原文

Engineering immune cells to treat hematological malignancies has been a major focus of research since the first resounding successes of CAR-T-cell therapies in B-ALL. Several diseases can now be treated in highly therapy-refractory or relapsed conditions. Currently, a number of CD19- or BCMA-specific CAR-T-cell therapies are approved for acute lymphoblastic leukemia (ALL), diffuse large B-cell lymphoma (DLBCL), mantle cell lymphoma (MCL), multiple myeloma (MM), and follicular lymphoma (FL). The implementation of these therapies has significantly improved patient outcome and survival even in cases with previously very poor prognosis. In this comprehensive review, we present the current state of research, recent innovations, and the applications of CAR-T-cell therapy in a selected group of hematologic malignancies. We focus on B- and T-cell malignancies, including the entities of cutaneous and peripheral T-cell lymphoma (T-ALL, PTCL, CTCL), acute myeloid leukemia (AML), chronic myeloid leukemia (CML), chronic lymphocytic leukemia (CLL), classical Hodgkin-Lymphoma (HL), Burkitt-Lymphoma (BL), hairy cell leukemia (HCL), and Waldenstr m's macroglobulinemia (WM). While these diseases are highly heterogenous, we highlight several similarly used approaches (combination with established therapeutics, target depletion on healthy cells), targets used in multiple diseases (CD30, CD38, TRBC1/2), and unique features that require individualized approaches. Furthermore, we focus on current limitations of CAR-T-cell therapy in individual diseases and entities such as immunocompromising tumor microenvironment (TME), risk of on-target-off-tumor effects, and differences in the occurrence of adverse events. Finally, we present an outlook into novel innovations in CAR-T-cell engineering like the use of artificial intelligence and the future role of CAR-T cells in therapy regimens in everyday clinical practice.

论文信息

作者
Karsten H、Matrisch L、Cichutek S、Fiedler W、Alsdorf W、Block A
第一作者单位
Faculty of Medicine, University of Hamburg, Hamburg, Germany.Germany
通讯作者单位
Department of Oncology, Hematology and Bone Marrow Transplantation with Division of Pneumology, University Medical Center Eppendorf, Hamburg, Germany.Germany
文献类型
综述 · 非美国政府资助研究
期刊
Frontiers in immunology2023
原文标识
PubMed 38090582 · DOI 10.3389/fimmu.2023.1285406