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桥接癌症和感染性疾病中多特异性免疫细胞衔接器的差距

英文原题:Bridging the gap with multispecific immune cell engagers in cancer and infectious diseases.

查看英文原题

Bridging the gap with multispecific immune cell engagers in cancer and infectious diseases.

PubMed 2024/05/24(内容时间) Cell Mol Immunol Q1 · IF 23.9(JCR 2025)

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中文摘要

通过同时结合多个抗原,多特异性抗体有望显著提高基于抗体的免疫疗法的活性和长期疗效。免疫细胞衔接器是抗体类构建体的一个亚类,由工程化结构组成,旨在将免疫效应细胞桥接至其靶标,从而将免疫应答重定向至肿瘤细胞或感染细胞。近期评估免疫细胞衔接器的临床试验数量不断增加,反映了这些分子在癌症和感染新型治疗策略中的重要作用。在这篇综述中,我们讨论了在癌症和感染性疾病的免疫治疗中,不同免疫细胞类型(T淋巴细胞和自然杀伤淋巴细胞,以及髓系细胞)如何被免疫细胞衔接器结合。此外,我们探讨了这些构建体的临床前和临床进展,并讨论了将当前来自癌症领域的知识转化至病毒学领域所面临的挑战。最后,我们推测了免疫细胞衔接器在癌症治疗和抗病毒治疗中可能采取的有前景的未来方向。

展开英文摘要原文

By binding to multiple antigens simultaneously, multispecific antibodies are expected to substantially improve both the activity and long-term efficacy of antibody-based immunotherapy. Immune cell engagers, a subclass of antibody-based constructs, consist of engineered structures designed to bridge immune effector cells to their target, thereby redirecting the immune response toward the tumor cells or infected cells.

The increasing number of recent clinical trials evaluating immune cell engagers reflects the important role of these molecules in new therapeutic approaches for cancer and infections. In this review, we discuss how different immune cell types (T and natural killer lymphocytes, as well as myeloid cells) can be bound by immune cell engagers in immunotherapy for cancer and infectious diseases.

Furthermore, we explore the preclinical and clinical advancements of these constructs, and we discuss the challenges in translating the current knowledge from cancer to the virology field.

Finally, we speculate on the promising future directions that immune cell engagers may take in cancer treatment and antiviral therapy.

论文信息

作者
Rolin C、Zimmer J、Seguin-Devaux C
单位
Department of Infection and Immunity, Luxembourg Institute of Health, 29 Rue Henri Koch, L-4354, Esch-Sur-Alzette, Luxembourg. camille.rolin@lih.lu.Luxembourg
文献类型
综述
期刊
Cellular & molecular immunology2024 Jul
原文标识
PubMed 38789528 · DOI 10.1038/s41423-024-01176-4