Title: Proceedings 31st Symposium ESVN-ECVN Document date: 2019_12_21
ID: 4526ne4l_110
Snippet: Human gliomas appear to exploit immune inhibitory mechanisms to maintain an immunosuppressive microenvironment and evade immune eradication. Binding of programmed cell death protein 1 (PDâ€1) to its ligand (PDâ€L1) promotes activated Tâ€cell exhaustion and apoptosis. Tumour cells (TCs) evade host's immune attack by expressing PDâ€L1 and stimulating PDâ€1 expression on tumourâ€infiltrating lymphocytes (TILs). Highâ€grade and astrocytic glio.....
Document: Human gliomas appear to exploit immune inhibitory mechanisms to maintain an immunosuppressive microenvironment and evade immune eradication. Binding of programmed cell death protein 1 (PDâ€1) to its ligand (PDâ€L1) promotes activated Tâ€cell exhaustion and apoptosis. Tumour cells (TCs) evade host's immune attack by expressing PDâ€L1 and stimulating PDâ€1 expression on tumourâ€infiltrating lymphocytes (TILs). Highâ€grade and astrocytic gliomas express higher levels of PDâ€L1 and immunotherapeutic targeting of the PDâ€1â€PDâ€L1 pathway is intensely studied; however, clinical evidence supporting these strategies’ efficacy is lacking.
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