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10.1038/cddis.2015.162

http://scihub22266oqcxt.onion/10.1038/cddis.2015.162
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C4669840!4669840 !26086965
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suck abstract from ncbi


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pmid26086965
      Cell+Death+Dis 2015 ; 6 (6 ): e1792
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  • T-cell exhaustion in the tumor microenvironment #MMPMID26086965
  • Jiang Y ; Li Y ; Zhu B
  • Cell Death Dis 2015[Jun]; 6 (6 ): e1792 PMID26086965 show ga
  • T-cell exhaustion was originally identified during chronic infection in mice, and was subsequently observed in humans with cancer. The exhausted T cells in the tumor microenvironment show overexpressed inhibitory receptors, decreased effector cytokine production and cytolytic activity, leading to the failure of cancer elimination. Restoring exhausted T cells represents an inspiring strategy for cancer treatment, which has yielded promising results and become a significant breakthrough in the cancer immunotherapy. In this review, we overview the updated understanding on the exhausted T cells in cancer and their potential regulatory mechanisms and discuss current therapeutic interventions targeting exhausted T cells in clinical trials.
  • |Animals [MESH]
  • |Basic-Leucine Zipper Transcription Factors/metabolism [MESH]
  • |Cytokines/metabolism [MESH]
  • |Humans [MESH]
  • |Lymphocyte Activation/immunology [MESH]
  • |Mice [MESH]
  • |NFATC Transcription Factors/metabolism [MESH]
  • |Neoplasms/*immunology [MESH]
  • |Positive Regulatory Domain I-Binding Factor 1 [MESH]
  • |Programmed Cell Death 1 Receptor/genetics/metabolism [MESH]
  • |Repressor Proteins/metabolism [MESH]
  • |T-Box Domain Proteins/metabolism [MESH]
  • |T-Lymphocytes/*immunology [MESH]
  • |T-bet Transcription Factor [MESH]
  • |Tumor Escape/*immunology [MESH]


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