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工程化 T 细胞受体样抗体用于生物制剂和细胞治疗。

Engineering T-cell receptor-like antibodies for biologics and cell therapy.

机构信息

Nextera AS, Gaustadalléen 21, N-0349 Oslo, Norway.

Nextera AS, Gaustadalléen 21, N-0349 Oslo, Norway.

出版信息

Curr Opin Biotechnol. 2024 Dec;90:103224. doi: 10.1016/j.copbio.2024.103224. Epub 2024 Nov 4.

DOI:10.1016/j.copbio.2024.103224
PMID:39488859
Abstract

A major prevailing challenge limiting our ability to fully harness the potential of the latest-generation therapeutic antibodies is the scarcity of clinically established disease-specific targets. A major next step forward will therefore be to expand this target space. The recent clinical success of immunotherapies such as adoptive T-cell transfer, immune checkpoint inhibition, and chimeric antigen receptor (CAR) T-cell therapy strongly supports focusing on the immunopeptidome of peptides presented by human leukocyte antigen (pHLA) that are normally surveilled by T-cell receptors (TCRs). Directing novel antibody development toward pHLA targets has given rise to TCR-like antibodies, which reached the clinic in 2020, as both bispecific T-cell engaging antibodies and the CARs of CAR-T cell therapies. In this review, we highlight recent advances in TCR-like antibodies, including therapeutic modalities, engineering strategies, and benchmarks for success.

摘要

限制我们充分利用最新一代治疗性抗体潜力的主要挑战是临床确立的疾病特异性靶标的稀缺性。因此,下一步的主要目标将是扩大这一靶标范围。最近免疫疗法的临床成功,如过继性 T 细胞转移、免疫检查点抑制和嵌合抗原受体 (CAR) T 细胞疗法,强烈支持关注人类白细胞抗原 (pHLA) 呈递的免疫肽组,这些肽通常受到 T 细胞受体 (TCR) 的监测。将新型抗体的开发方向指向 pHLA 靶标产生了 TCR 样抗体,这些抗体在 2020 年作为双特异性 T 细胞结合抗体和 CAR-T 细胞疗法的 CAR 进入临床。在这篇综述中,我们强调了 TCR 样抗体的最新进展,包括治疗方式、工程策略和成功基准。

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