1. Programmed cell death ligand-1: A dynamic immune checkpoint in cancer therapy.
- Author
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Kalim M, Iqbal Khan MS, and Zhan J
- Subjects
- Animals, Antibodies, Monoclonal pharmacology, Antineoplastic Agents metabolism, Antineoplastic Agents pharmacology, Apoptosis drug effects, Cell Proliferation drug effects, Cytokines metabolism, Gene Expression Regulation drug effects, Humans, Immune Checkpoint Inhibitors metabolism, Immune Checkpoint Inhibitors pharmacology, Immunotherapy methods, Ligands, Lymphocyte Activation drug effects, Programmed Cell Death 1 Receptor genetics, T-Lymphocytes drug effects, T-Lymphocytes immunology, Antibodies, Monoclonal chemistry, Antineoplastic Agents chemistry, Immune Checkpoint Inhibitors chemistry, Pharmaceutical Preparations chemistry, Programmed Cell Death 1 Receptor antagonists & inhibitors
- Abstract
Antibody-based immunotherapies play a pivotal role in cancer research with efficient achievements in tumor suppression. Tumor survival is assisted by modulation of immune checkpoints to create imbalances between immune cells and cancer cell's environment. The modulation results in T-cell signal inhibition ultimately inert its proliferation and activation against various tumor cells. PD-L1, a 40 kDa transmembrane protein of B7 family, binds with PD-1 on the membrane of T cells which results in inhibition of T-cell proliferation and activation. PD-L1/PD-1 pathway has generated novel target sites for antibodies that can block PD-L1/PD-1 interactions. The blockage results in T-cell proliferation and tumor cell suppression. The PD-L1 immune checkpoint strategies' development, expression and regulations, signal inhibitions, and developmental stages of PD-L1/PD-1 antibodies are briefly discussed here in this review. All this information will provide a base for new therapeutic development against PD-L1 and PD-1 immune checkpoint interactions and will make available promising treatment options., (© 2020 John Wiley & Sons A/S.)
- Published
- 2020
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