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Preclinical Evaluation of CAR T Cell Function: In Vitro and In Vivo Models.
Si, Xiaohui; Xiao, Lu; Brown, Christine E; Wang, Dongrui.
Affiliation
  • Si X; Bone Marrow Transplantation Center of the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China.
  • Xiao L; Liangzhu Laboratory, Zhejiang University Medical Center, 1369 West Wenyi Road, Hangzhou 311121, China.
  • Brown CE; Institute of Hematology, Zhejiang University, Hangzhou 310030, China.
  • Wang D; Zhejiang Province Engineering Laboratory for Stem Cell and Immunity Therapy, Hangzhou 310030, China.
Int J Mol Sci ; 23(6)2022 Mar 15.
Article in En | MEDLINE | ID: mdl-35328572
ABSTRACT
Immunotherapy using chimeric antigen receptor (CAR) T cells is a rapidly emerging modality that engineers T cells to redirect tumor-specific cytotoxicity. CAR T cells have been well characterized for their efficacy against B cell malignancies, and rigorously studied in other types of tumors. Preclinical evaluation of CAR T cell function, including direct tumor killing, cytokine production, and memory responses, is crucial to the development and optimization of CAR T cell therapies. Such comprehensive examinations are usually performed in different types of models. Model establishment should focus on key challenges in the clinical setting and the capability to generate reliable data to indicate CAR T cell therapeutic potency in the clinic. Further, modeling the interaction between CAR T cells and tumor microenvironment provides additional insight for the future endeavors to enhance efficacy, especially against solid tumors. This review will summarize both in vitro and in vivo models for CAR T cell functional evaluation, including how they have evolved with the needs of CAR T cell research, the information they can provide for preclinical assessment of CAR T cell products, and recent technology advances to test CAR T cells in more clinically relevant models.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Chimeric Antigen / Neoplasms Limits: Humans Language: En Journal: Int J Mol Sci Year: 2022 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Chimeric Antigen / Neoplasms Limits: Humans Language: En Journal: Int J Mol Sci Year: 2022 Document type: Article Affiliation country: China