T Cell Exhaustion and CAR-T Immunotherapy in Hematological Malignancies
- PMID: 33728333
- PMCID: PMC7936901
- DOI: 10.1155/2021/6616391
T Cell Exhaustion and CAR-T Immunotherapy in Hematological Malignancies
Abstract
T cell exhaustion has been recognized to play an immunosuppressive role in malignant diseases. Persistent tumor antigen stimulation, the presence of inhibitory immune cells and cytokines in tumor microenvironment (TME), upregulated expression of inhibitory receptors, changes in T cell-related transcription factors, and metabolic factors can all result in T cell exhaustion. Strategies dedicated to preventing or reversing T cell exhaustion are required to reduce the morbidity from cancer and enhance the effectiveness of adoptive cellular immunotherapy. Here, we summarize the current findings of T cell exhaustion in hematological malignancies and chimeric antigen receptor T (CAR-T) immunotherapy, as well as the value of novel technologies, to inverse such dysfunction. Our emerging understanding of T cell exhaustion may be utilized to develop personalized strategies to restore antitumor immunity.
Copyright © 2021 Lu Tang et al.
Conflict of interest statement
The authors declare that they have no conflict of interest.
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- Gallimore A., Glithero A., Godkin A., et al. Induction and exhaustion of lymphocytic choriomeningitis virus-specific cytotoxic T lymphocytes visualized using soluble tetrameric major histocompatibility complex class I-peptide complexes. The Journal of Experimental Medicine. 1998;187(9):1383–1393. doi: 10.1084/jem.187.9.1383. - DOI - PMC - PubMed
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