Advancements and challenges in developing in vivo CAR T cell therapies for cancer treatment

被引:31
作者
Bui, Thuy Anh [1 ,2 ,5 ]
Mei, Haoqi [1 ]
Sang, Rui [3 ]
Ortega, David Gallego [1 ,4 ,5 ]
Deng, Wei [1 ,3 ]
机构
[1] Univ Technol Sydney, Sch Biomed Engn, Ultimo, NSW 2007, Australia
[2] Ingham Inst Appl Med Res, Whitlam Orthopaed Res Ctr, Liverpool, NSW 2170, Australia
[3] UNSW Sydney, Fac Engn, ARC Ctr Excellence Nanoscale Biophoton, Grad Sch Biomed Engn, Sydney, NSW 2052, Australia
[4] Kinghorn Canc Ctr, Garvan Inst Med Res, Darlinghurst, NSW 2010, Australia
[5] Univ New South Wales Sydney, Fac Med, Sch Clin Med, Kensington, NSW 2052, Australia
关键词
Cancer; In vivo CAR-T; Gene editing; Gene delivery; CHIMERIC-ANTIGEN-RECEPTOR; LIPID NANOPARTICLES; MESSENGER-RNA; GENE-TRANSFER; DELIVERY; LYMPHOCYTES; ACTIVATION; EXPRESSION; PATHWAYS; VECTORS;
D O I
10.1016/j.ebiom.2024.105266
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Chimeric Antigen Receptor (CAR) T cell therapy has emerged as a ground-breaking immunotherapeutic approach in cancer treatment. To overcome the complexity and high manufacturing cost associated with current ex vivo CAR T cell therapy products, alternative strategies to produce CAR T cells directly in the body have been developed in recent years. These strategies involve the direct infusion of CAR genes via engineered nanocarriers or viral vectors to generate CAR T cells in situ. . This review offers a comprehensive overview of recent advancements in the development of T cell-targeted CAR generation in situ. . Additionally, it identifies fi es the challenges associated with in vivo CAR T method and potential strategies to overcome these issues. Copyright (c) 2024 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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页数:14
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