Literature DB >> 32185706

Roles of PD-1/PD-L1 Pathway: Signaling, Cancer, and Beyond.

Luoyan Ai1, Antao Xu2, Jie Xu3.   

Abstract

Immunotherapies that target PD-1/PD-L1 axis have shown unprecedented success in a wide variety of human cancers. PD-1 is one of the key coinhibitory receptors expressed on T cells upon T cell activation. After engagement with its ligands, mainly PD-L1, PD-1 is activated and recruits the phosphatase SHP-2 in proximity to T cell receptor (TCR) and CD28 signaling. This event results in dephosphorylation and attenuation of key molecules in TCR and CD28 pathway, leading to inhibition of T cell proliferation, activation, cytokine production, altered metabolism and cytotoxic T lymphocytes (CTLs) killer functions, and eventual death of activated T cells. Bodies evolve coinhibitory pathways controlling T cell response magnitude and duration to limit tissue damage and maintain self-tolerance. However, tumor cells hijack these inhibitory pathways to escape host immune surveillance by overexpression of PD-L1. This provides the scientific rationale for clinical application of immune checkpoint inhibitors in oncology. The aberrantly high expression of PD-L1 in tumor microenvironment (TME) can be attributable to the "primary" activation of multiple oncogenic signaling and the "secondary" induction by inflammatory factors such as IFN-γ. Clinically, antibodies targeting PD-1/PD-L1 reinvigorate the "exhausted" T cells in TME and show remarkable objective response and durable remission with acceptable toxicity profile in large numbers of tumors such as melanoma, lymphoma, and mismatch-repair deficient tumors. Nevertheless, most patients are still refractory to anti-PD-1/PD-L1 therapy. Identifying the predictive biomarkers and design rational PD-1-based combination therapy become the priorities in cancer immunotherapy. PD-L1 expression, cytotoxic T lymphocytes infiltration, and tumor mutation burden (TMB) are generally considered as the most important factors affecting the effectiveness of PD-1/PD-L1 blockade. The revolution in cancer immunotherapy achieved by PD-1/PD-L1 blockade offers the paradigm for scientific translation from bench to bedside. The next decades will without doubt witness the renaissance of immunotherapy.

Entities:  

Keywords:  Cancer immune evasion; PD-1; PD-L1; Self-tolerance; T cell inhibition

Year:  2020        PMID: 32185706     DOI: 10.1007/978-981-15-3266-5_3

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  56 in total

1.  Genomic, Immunological, and Clinical Characterization of Pyroptosis in Ovarian Cancer.

Authors:  Min Zhou; Bingshu Li; Jianfeng Liu; Li Hong
Journal:  J Inflamm Res       Date:  2021-12-24

2.  A signature based on m6A pattern and tumor microenvironment infiltration in clear cell renal cell carcinoma.

Authors:  Chen Yang; Tian Yu; Qingwen Li; Fang Xie; Qin Lin
Journal:  Am J Transl Res       Date:  2022-07-15       Impact factor: 3.940

Review 3.  Dendrimers for cancer immunotherapy: Avidity-based drug delivery vehicles for effective anti-tumor immune response.

Authors:  Piper A Rawding; Jiyoon Bu; Jianxin Wang; Da Won Kim; Adam J Drelich; Youngsoo Kim; Seungpyo Hong
Journal:  Wiley Interdiscip Rev Nanomed Nanobiotechnol       Date:  2021-08-19

4.  Self-reactive, innate-like T cells enhance cytotoxicity and immunosurveillance.

Authors:  Blaire E Barton; Cindy H Chau; William D Figg
Journal:  Trends Cancer       Date:  2022-06-04

5.  IL4I1 enhances PD-L1 expression through JAK/STAT signaling pathway in lung adenocarcinoma.

Authors:  Jiefei Zhu; Yan Li; Xu Lv
Journal:  Immunogenetics       Date:  2022-09-03       Impact factor: 3.330

6.  Donor T cell DNMT3a regulates alloreactivity in mouse models of hematopoietic stem cell transplantation.

Authors:  Yiouli P Ktena; Michael A Koldobskiy; Michael I Barbato; Han-Hsuan Fu; Leo Luznik; Nicolas J Llosa; Azeb Haile; Orly R Klein; Chen Liu; Christopher J Gamper; Kenneth R Cooke
Journal:  J Clin Invest       Date:  2022-07-01       Impact factor: 19.456

7.  Clustering analysis and prognostic signature of lung adenocarcinoma based on the tumor microenvironment.

Authors:  Qingqing Shan; Yifan Zhang; Zongan Liang
Journal:  Sci Rep       Date:  2022-07-14       Impact factor: 4.996

8.  A Small Molecule Antagonist of PD-1/PD-L1 Interactions Acts as an Immune Checkpoint Inhibitor for NSCLC and Melanoma Immunotherapy.

Authors:  Yuanyuan Wang; Tingxuan Gu; Xueli Tian; Wenwen Li; Ran Zhao; Wenqian Yang; Quanli Gao; Tiepeng Li; Jung-Hyun Shim; Chengjuan Zhang; Kangdong Liu; Mee-Hyun Lee
Journal:  Front Immunol       Date:  2021-05-14       Impact factor: 7.561

9.  Programmed Death-Ligand 1 (PD-L1) Expression Is Induced by Insulin in Pancreatic Ductal Adenocarcinoma Cells Pointing to Its Role in Immune Checkpoint Control.

Authors:  Steffen M Heckl; Franziska Mau; Anke Senftleben; Tina Daunke; Silje Beckinger; Samir Abdullazade; Stefan Schreiber; Christoph Röcken; Susanne Sebens; Heiner Schäfer
Journal:  Med Sci (Basel)       Date:  2021-06-25

10.  Histone deacetylase 2 knockout suppresses immune escape of triple-negative breast cancer cells via downregulating PD-L1 expression.

Authors:  Pengfei Xu; Wei Xiong; Yun Lin; Liping Fan; Hongchao Pan; Yaochen Li
Journal:  Cell Death Dis       Date:  2021-08-07       Impact factor: 8.469

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