| Literature DB >> 33374128 |
Marsha Pellegrino1, Francesca Del Bufalo1, Biagio De Angelis1, Concetta Quintarelli1,2, Ignazio Caruana1,3, Emmanuel de Billy1.
Abstract
The adoptive transfer of the chimeric antigen receptor (CAR) expressing T-cells has produced unprecedented successful results in the treatment of B-cell malignancies. However, the use of this technology in other malignancies remains less effective. In the setting of solid neoplasms, CAR T-cell metabolic fitness needs to be optimal to reach the tumor and execute their cytolytic function in an environment often hostile. It is now well established that both tumor and T cell metabolisms play critical roles in controlling the immune response by conditioning the tumor microenvironment and the fate and activity of the T cells. In this review, after a brief description of the tumoral and T cell metabolic reprogramming, we summarize the latest advances and new strategies that have been developed to improve the metabolic fitness and efficacy of CAR T-cell products.Entities:
Keywords: Chimeric Antigen Receptor T cells; cancer; combined therapy; immunotherapy; metabolic reprogramming
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Year: 2020 PMID: 33374128 PMCID: PMC7824126 DOI: 10.3390/cells10010014
Source DB: PubMed Journal: Cells ISSN: 2073-4409 Impact factor: 6.600