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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Chemical Biology & D...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Chemical Biology & Drug Design
Article . 2020 . Peer-reviewed
License: Wiley Online Library User Agreement
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Programmed cell death ligand‐1: A dynamic immune checkpoint in cancer therapy

Authors: Muhammad Kalim; Muhammad Saleem Iqbal Khan; Jinbiao Zhan;

Programmed cell death ligand‐1: A dynamic immune checkpoint in cancer therapy

Abstract

AbstractAntibody‐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.

Related Organizations
Keywords

T-Lymphocytes, Programmed Cell Death 1 Receptor, Antibodies, Monoclonal, Antineoplastic Agents, Apoptosis, Ligands, Lymphocyte Activation, Gene Expression Regulation, Pharmaceutical Preparations, Animals, Cytokines, Humans, Immunotherapy, Immune Checkpoint Inhibitors, Cell Proliferation

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    20
    popularity
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    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
20
Top 10%
Average
Top 10%
Related to Research communities
Cancer Research
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