Abstract |
Chimeric antigen receptor T (CAR-T) cell therapy achieved extraordinary achievements results in antitumor treatments, especially against hematological malignancies, where it leads to remarkable, long-term antineoplastic effects with higher target specificity. Nevertheless, some limitations persist in autologous CAR-T cell therapy, such as high costs, long manufacturing periods, and restricted cell sources. The development of a universal CAR-T (UCAR-T) cell therapy is an attractive breakthrough point that may overcome most of these drawbacks. Here, we review the progress and challenges in CAR-T cell therapy, especially focusing on comprehensive comparison in UCAR-T cell therapy to original CAR-T cell therapy. Furthermore, we summarize the developments and concerns about the safety and efficiency of UCAR-T cell therapy. Finally, we address other immune cells, which might be promising candidates as a complement for UCAR-T cells. Through a detailed overview, we describe the current landscape and explore the prospect of UCAR-T cell therapy.
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Authors | Haolong Lin, Jiali Cheng, Wei Mu, Jianfeng Zhou, Li Zhu |
Journal | Frontiers in immunology
(Front Immunol)
Vol. 12
Pg. 744823
( 2021)
ISSN: 1664-3224 [Electronic] Switzerland |
PMID | 34691052
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
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Copyright | Copyright © 2021 Lin, Cheng, Mu, Zhou and Zhu. |
Chemical References |
- Receptors, Chimeric Antigen
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Topics |
- Humans
- Immunotherapy, Adoptive
(methods, trends)
- Receptors, Chimeric Antigen
(therapeutic use)
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