将细胞疗法应用于肿瘤:最佳CAR粘合剂设计的考虑因素。

Q2 Medicine Antibody Therapeutics Pub Date : 2023-09-12 eCollection Date: 2023-10-01 DOI:10.1093/abt/tbad019
Richard Smith
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引用次数: 0

摘要

嵌合抗原受体(CAR)-T细胞已经彻底改变了B细胞恶性肿瘤的免疫疗法,并准备在广泛的肿瘤和非肿瘤适应症中扩大其影响范围。给定CAR成功的关键是结合结构域的选择,因为这是特异性的关键驱动因素,在决定细胞治疗的疗效、效力和持久性方面发挥着重要作用(与CAR结构的其余部分一起)。虽然抗体已被证明是CAR结合域的有效来源,但很明显,CAR结合结构域的所需属性与重组抗体的不同。这篇综述将讨论在为给定的CAR选择最佳结合域时需要考虑的关键因素,以及粘合剂性质如何影响CAR的其余部分。
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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Bringing cell therapy to tumors: considerations for optimal CAR binder design.

Chimeric antigen receptor (CAR)-T cells have revolutionized the immunotherapy of B-cell malignancies and are poised to expand the range of their impact across a broad range of oncology and non-oncology indications. Critical to the success of a given CAR is the choice of binding domain, as this is the key driver for specificity and plays an important role (along with the rest of the CAR structure) in determining efficacy, potency and durability of the cell therapy. While antibodies have proven to be effective sources of CAR binding domains, it has become apparent that the desired attributes for a CAR binding domain do differ from those of a recombinant antibody. This review will address key factors that need to be considered in choosing the optimal binding domain for a given CAR and how binder properties influence and are influenced by the rest of the CAR.

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来源期刊
Antibody Therapeutics
Antibody Therapeutics Medicine-Immunology and Allergy
CiteScore
8.70
自引率
0.00%
发文量
30
审稿时长
8 weeks
期刊最新文献
AI-based antibody discovery platform identifies novel, diverse, and pharmacologically active therapeutic antibodies against multiple SARS-CoV-2 strains. FcRider: a recombinant Fc nanoparticle with endogenous adjuvant activities for hybrid immunization. A pan-allelic human SIRPα-blocking antibody, ES004-B5, promotes tumor killing by enhancing macrophage phagocytosis and subsequently inducing an effective T-cell response. Correction to: A case study of a bispecific antibody manufacturability assessment and optimization during discovery stage and its implications. The process using a synthetic library that generates multiple diverse human single domain antibodies.
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