Next-generation in vivo CAR-T expansion strategies: Unlocking durable anti-tumor responses in solid tumors

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Authors: Zefeng Sun, Lihang Wei, Xinyi Pan, Wenyue Yan, Tingting Wang, Xinyue Wang
Cited by: 1
References: 86

Abstract

The efficacy of chimeric antigen receptor T (CAR-T) cell therapy is directly associated with the abundance of functionally active anti-tumor CAR-T cells. However, the complexity of CAR-T manufacturing limits clinical accessibility and increases the risk of disease progression during treatment preparation. To improve CAR-T production, multiple strategies have been developed to expand CAR-T cells either in vitro or in vivo, including genetic engineering, vaccine platforms, cytokine stimulation, and the application of nanoparticles, engineered bacteria, and their outer membrane vesicles (OMVs). With the advancement of in vivo CAR-T approaches, the development of biocompatible materials that enable safe and effective in vivo expansion has become increasingly important. This review systematically examines the challenges associated with in vivo CAR-T cell expansion in solid tumors, comprehensively summarizes the mechanisms, advantages, and limitations of current expansion platforms, and discusses their translational potential, providing practical insights to guide the development of in vivo CAR-T therapies.

Fields of Study & Subjects

CAR-T cell therapy research Virus-based gene therapy research Monoclonal and Polyclonal Antibodies Research

Publication details

Journal / source
Critical Reviews in Oncology/Hematology
Publisher
Elsevier BV
Volume
223
Pages
105342–105342
Publication date
19 April 2026
Language
EN