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工程化增强型嵌合抗原受体T细胞疗法治疗实体瘤。

Engineering enhanced chimeric antigen receptor-T cell therapy for solid tumors.

作者信息

Neeser A, Ramasubramanian R, Wang C, Ma L

机构信息

Department of Bioengineering, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia.

The Raymond G. Perelman Center for Cellular and Molecular Therapeutics, Children's Hospital of Philadelphia, Philadelphia.

出版信息

Immunooncol Technol. 2023 May 24;19:100385. doi: 10.1016/j.iotech.2023.100385. eCollection 2023 Sep.

Abstract

The early clinical success and subsequent US Food and Drug Administration approval of chimeric antigen receptor (CAR)-T cell therapy for leukemia and lymphoma affirm that engineered T cells can be a powerful treatment for hematologic malignancies. Yet this success has not been replicated in solid tumors. Numerous challenges emerged from clinical experience and well-controlled preclinical animal models must be met to enable safe and efficacious CAR-T cell therapy in solid tumors. Here, we review recent advances in bioengineering strategies developed to enhance CAR-T cell therapy in solid tumors, focusing on targeted single-gene perturbation, genetic circuits design, cytokine engineering, and interactive biomaterials. These bioengineering approaches present a unique set of tools that synergize with CAR-T cells to overcome obstacles in solid tumors and achieve robust and long-lasting therapeutic efficacy.

摘要

嵌合抗原受体(CAR)-T细胞疗法在白血病和淋巴瘤治疗中取得的早期临床成功以及随后获得美国食品药品监督管理局的批准,证实了工程化T细胞可以成为治疗血液系统恶性肿瘤的有力手段。然而,这种成功尚未在实体瘤中得到复制。临床经验带来了诸多挑战,必须克服精心控制的临床前动物模型中的问题,才能在实体瘤中实现安全有效的CAR-T细胞疗法。在此,我们回顾了为增强实体瘤中CAR-T细胞疗法而开发的生物工程策略的最新进展,重点关注靶向单基因扰动、基因回路设计、细胞因子工程和交互式生物材料。这些生物工程方法提供了一套独特的工具,可与CAR-T细胞协同作用,克服实体瘤中的障碍,实现强大而持久的治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20fc/10362352/bfa94036d9d4/gr1.jpg

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