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Synthetic Cells and Molecules in Cellular Immunotherapy.

Authors :
Lin H
Li C
Zhang W
Wu B
Wang Y
Wang S
Wang D
Li X
Huang H
Source :
International journal of biological sciences [Int J Biol Sci] 2024 May 11; Vol. 20 (8), pp. 2833-2859. Date of Electronic Publication: 2024 May 11 (Print Publication: 2024).
Publication Year :
2024

Abstract

Cellular immunotherapy has emerged as an exciting strategy for cancer treatment, as it aims to enhance the body's immune response to tumor cells by engineering immune cells and designing synthetic molecules from scratch. Because of the cytotoxic nature, abundance in peripheral blood, and maturation of genetic engineering techniques, T cells have become the most commonly engineered immune cells to date. Represented by chimeric antigen receptor (CAR)-T therapy, T cell-based immunotherapy has revolutionized the clinical treatment of hematological malignancies. However, serious side effects and limited efficacy in solid tumors have hindered the clinical application of cellular immunotherapy. To address these limitations, various innovative strategies regarding synthetic cells and molecules have been developed. On one hand, some cytotoxic immune cells other than T cells have been engineered to explore the potential of targeted elimination of tumor cells, while some adjuvant cells have also been engineered to enhance the therapeutic effect. On the other hand, diverse synthetic cellular components and molecules are added to engineered immune cells to regulate their functions, promoting cytotoxic activity and restricting side effects. Moreover, novel bioactive materials such as hydrogels facilitating the delivery of therapeutic immune cells have also been applied to improve the efficacy of cellular immunotherapy. This review summarizes the innovative strategies of synthetic cells and molecules currently available in cellular immunotherapies, discusses the limitations, and provides insights into the next generation of cellular immunotherapies.<br />Competing Interests: Competing Interests: The authors have declared that no competing interest exists.<br /> (© The author(s).)

Details

Language :
English
ISSN :
1449-2288
Volume :
20
Issue :
8
Database :
MEDLINE
Journal :
International journal of biological sciences
Publication Type :
Academic Journal
Accession number :
38904025
Full Text :
https://doi.org/10.7150/ijbs.94346