Bispecific antibodies (bsAbs) directed against PD-1/PD-L1 and CTLA-4; a mini review.

Q3 Medicine
Amirhossein Mardi, Leili Aghebati-Maleki
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引用次数: 0

Abstract

Novel approaches to tumor immunotherapy include adoptive cell immunotherapy, immune checkpoint inhibitors (ICIs), and bispecific antibodies (bsABs). bsABs are members of the antibody family that have the ability to distinguish between two distinct antigens or epitopes on a single antigen. These antibodies show better clinical results than monoclonal antibodies, suggesting that they might be a useful choice for tumor immunotherapy. Additionally, dual blockade immunotherapy targeting PD-1/PD-L1 and CTLA-4 functions at various phases of T cell activation with synergistically increasing immune responses against cancer cells, in contrast to ICI monotherapy, which sometimes displays treatment resistance and limited effectiveness. It has been shown that immune response rates and anti-tumor effects may be increased in a synergistic manner by ICI-based combination therapy. We explore the safety and effectiveness of bsABs and ICIs (especially PD1/PDL1 and CTLA-4) combination treatments in tumor immunotherapy in this study with the goal of offering evidence-based methods for clinical research and tailored tumor identification and management.

针对PD-1/PD-L1和CTLA-4的双特异性抗体(bsAbs);一个小回顾。
肿瘤免疫治疗的新方法包括过继细胞免疫治疗、免疫检查点抑制剂(ICIs)和双特异性抗体(bsABs)。bsab是抗体家族的成员,具有区分单一抗原上的两种不同抗原或表位的能力。这些抗体比单克隆抗体表现出更好的临床效果,提示它们可能是肿瘤免疫治疗的有用选择。此外,靶向PD-1/PD-L1和CTLA-4的双重阻断免疫疗法在T细胞活化的各个阶段发挥作用,协同增加对癌细胞的免疫反应,与ICI单一疗法相比,后者有时表现出治疗耐药性和有限的有效性。已有研究表明,免疫应答率和抗肿瘤作用可能以协同方式增加基于ci的联合治疗。本研究探讨bsABs和ICIs(特别是PD1/PDL1和CTLA-4)联合治疗在肿瘤免疫治疗中的安全性和有效性,旨在为临床研究和量身定制的肿瘤识别和管理提供循证方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Human Antibodies
Human Antibodies Medicine-Immunology and Allergy
CiteScore
3.50
自引率
0.00%
发文量
27
期刊介绍: Human Antibodies is an international journal designed to bring together all aspects of human hybridomas and antibody technology under a single, cohesive theme. This includes fundamental research, applied science and clinical applications. Emphasis in the published articles is on antisera, monoclonal antibodies, fusion partners, EBV transformation, transfections, in vitro immunization, defined antigens, tissue reactivity, scale-up production, chimeric antibodies, autoimmunity, natural antibodies/immune response, anti-idiotypes, and hybridomas secreting interesting growth factors. Immunoregulatory molecules, including T cell hybridomas, will also be featured.
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