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Tumor Biology
Erschienen in: Tumor Biology 4/2016

16.01.2016 | Review

Potential biomarker for checkpoint blockade immunotherapy and treatment strategy

verfasst von: Zhong-Yi Dong, Si-Pei Wu, Ri-Qiang Liao, Shu-Mei Huang, Yi-Long Wu

Erschienen in: Tumor Biology | Ausgabe 4/2016

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Abstract

Programmed cell death protein-1 (PD-1) and ligand (PD-L1) provide an important escape mechanism from immune attack, and blockade therapy of these proteins show promising clinical benefits in many types of cancer. PD-L1 can be induced by interferon-gamma (IFN-γ), hypoxia, or toll-like receptor (TLR)-mediated pathways that confer adaptive immune resistance, or upregulated by oncogenic signals leading to constitutive expression and resulting in intrinsic immune resistance. The PD-1/PD-L1 checkpoint blockade, which targets regulatory pathways in T cells to overcome immune resistance, is correlated to PD-L1 expression pattern and the presence of tumor-infiltrating lymphocytes (TILs). Meanwhile, immunogenic mutation loads show significant response to checkpoint blockade, which is probably due to PD-1/L1 status and TIL content. Finally, the clinical strategies to design effective checkpoint-targeting immunotherapies are based on the classification of inducible/constitutive expression of PD-L1 and the presence of TILs.
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Metadaten
Titel
Potential biomarker for checkpoint blockade immunotherapy and treatment strategy
verfasst von
Zhong-Yi Dong
Si-Pei Wu
Ri-Qiang Liao
Shu-Mei Huang
Yi-Long Wu
Publikationsdatum
16.01.2016
Verlag
Springer Netherlands
Erschienen in
Tumor Biology / Ausgabe 4/2016
Print ISSN: 1010-4283
Elektronische ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-016-4812-9

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