| Literature DB >> 26674251 |
Madhusudhanan Sukumar1, Jie Liu2, Gautam U Mehta3, Shashank J Patel4, Rahul Roychoudhuri3, Joseph G Crompton3, Christopher A Klebanoff5, Yun Ji6, Peng Li7, Zhiya Yu3, Greg D Whitehill8, David Clever9, Robert L Eil3, Douglas C Palmer3, Suman Mitra7, Mahadev Rao10, Keyvan Keyvanfar8, David S Schrump10, Ena Wang11, Francesco M Marincola11, Luca Gattinoni6, Warren J Leonard7, Pawel Muranski8, Toren Finkel2, Nicholas P Restifo12.
Abstract
Long-term survival and antitumor immunity of adoptively transferred CD8(+) T cells is dependent on their metabolic fitness, but approaches to isolate therapeutic T cells based on metabolic features are not well established. Here we utilized a lipophilic cationic dye tetramethylrhodamine methyl ester (TMRM) to identify and isolate metabolically robust T cells based on their mitochondrial membrane potential (ΔΨm). Comprehensive metabolomic and gene expression profiling demonstrated global features of improved metabolic fitness in low-ΔΨm-sorted CD8(+) T cells. Transfer of these low-ΔΨm T cells was associated with superior long-term in vivo persistence and an enhanced capacity to eradicate established tumors compared with high-ΔΨm cells. Use of ΔΨm-based sorting to enrich for cells with superior metabolic features was observed in CD8(+), CD4(+) T cell subsets, and long-term hematopoietic stem cells. This metabolism-based approach to cell selection may be broadly applicable to therapies involving the transfer of HSC or lymphocytes for the treatment of viral-associated illnesses and cancer.Entities:
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Year: 2015 PMID: 26674251 PMCID: PMC4747432 DOI: 10.1016/j.cmet.2015.11.002
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287