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10.18632/oncotarget.13895

http://scihub22266oqcxt.onion/10.18632/oncotarget.13895
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C5356790!5356790!27974689
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suck abstract from ncbi


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pmid27974689      Oncotarget 2017 ; 8 (2): 2171-86
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  • PD-1 and its ligands are important immune checkpoints in cancer #MMPMID27974689
  • Dong Y; Sun Q; Zhang X
  • Oncotarget 2017[Jan]; 8 (2): 2171-86 PMID27974689show ga
  • Checkpoint programmed death-1 (PD-1)/programmed cell death ligands (PD-Ls) have been identified as negative immunoregulatory molecules that promote immune evasion of tumor cells. The interaction of PD-1 and PD-Ls inhibits the function of T cells and tumor-infiltrating lymphocytes (TIL) while increasing the function of immunosuppressive regulatory T cells (Tregs). This condition causes the tumor cells to evade immune response. Thus, the blockade of PD-1/PD-L1 enhances anti-tumor immunity by reducing the number and/or the suppressive activity of Tregs and by restoring the activity of effector T cells. Furthermore, some monoclonal antibodies blockading PD-1/PD-Ls axis have achieved good effect and received Food and Drug Administration approval. The role of PD-1/PD-Ls in tumors has been well studied, but little is known on the mechanism by which PD-1 blocks T-cell activation. In this study, we provide a brief overview on the discovery and regulatory mechanism of PD-1 and PD-L1 dysregulation in tumors, as well as the function and signaling pathway of PD-1 and its ligands; their roles in tumor evasion and clinical treatment were also studied.
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