Evidence map›Paper›PMID 33193345›Full record

ReviewFrontiers in immunology2020

The Extrinsic and Intrinsic Roles of PD-L1 and Its Receptor PD-1: Implications for Immunotherapy Treatment.

Katie Hudson, Neil Cross, Nicola Jordan-Mahy, Rebecca Leyland

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 154 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
154citing papers in PubMed, 8 pooled it
10.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

154 citing papers in PubMed, 8 syntheses or guidelines pooled it, 238 citations in OpenAlex.

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94 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Katie HudsonBiomolecular Sciences Research Centre, Sheffield Hallam University, Sheffield, United Kingdom.
Neil CrossBiomolecular Sciences Research Centre, Sheffield Hallam University, Sheffield, United Kingdom.
Nicola Jordan-MahyBiomolecular Sciences Research Centre, Sheffield Hallam University, Sheffield, United Kingdom.
Rebecca LeylandBiomolecular Sciences Research Centre, Sheffield Hallam University, Sheffield, United Kingdom.
Sheffield Hallam University · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Programmed death-ligand 1 (PD-L1) is an immune checkpoint inhibitor that binds to its receptor PD-1 expressed by T cells and other immune cells to regulate immune responses; ultimately preventing exacerbated activation and autoimmunity. Many tumors exploit this mechanism by overexpressing PD-L1 which often correlates with poor prognosis. Some tumors have also recently been shown to express PD-1. On tumors, PD-L1 binding to PD-1 on immune cells promotes immune evasion and tumor progression, primarily by inhibition of cytotoxic T lymphocyte effector function. PD-1/PD-L1-targeted therapy has revolutionized the cancer therapy landscape and has become the first-line treatment for some cancers, due to their ability to promote durable anti-tumor immune responses in select patients with advanced cancers. Despite this clinical success, some patients have shown to be unresponsive, hyperprogressive or develop resistance to PD-1/PD-L1-targeted therapy. The exact mechanisms for this are still unclear. This review will discuss the current status of PD-1/PD-L1-targeted therapy, oncogenic expression of PD-L1, the new and emerging tumor-intrinisic roles of PD-L1 and its receptor PD-1 and how they may contribute to tumor progression and immunotherapy responses as shown in different oncology models.

Indexed as

Immune Checkpoint ProteinsAnimalsAntineoplastic AgentsB7-H1 AntigenBiomarkers, TumorEnergy MetabolismEpigenesis, GeneticGene Expression Regulation, NeoplasticHumansImmune Checkpoint InhibitorsImmunomodulationMolecular Targeted TherapyNeoplasm MetastasisNeoplasmsProgrammed Cell Death 1 ReceptorSignal TransductionAntineoplastic AgentsB7-H1 AntigenBiomarkers, TumorCD274 protein, humanImmune Checkpoint InhibitorsImmune Checkpoint ProteinsProgrammed Cell Death 1 Receptorbiomarkersimmunotherapynovel therapeutic strategiesoncology modelsPD-1PD-1/PD-L1-targeted therapyprogrammed death-ligand 1tumor-intrinsic role

Identifiers

PMID33193345
PMCPMC7609400
OpenAlexW3093533116

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.