Evidence map›Paper›PMID 37036990›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

Blockade of trans PD-L1 interaction with CD80 augments antitumor immunity.

Yuankun Zhang, Qingxiao Song, Kaniel Cassady, Michael Lee, Haidong Tang, Moqian Zheng, Bixin Wang, Dustin E Schones, Yang-Xin Fu, Arthur D Riggs and 3 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
7.8field-weighted citation impact, top 2% 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

26 citing papers in PubMed, 34 citations in OpenAlex.

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  11. Emerging new immune checkpoint inhibitors in solid tumor immunotherapy.Naunyn-Schmiedeberg's archives of pharmacology · 2025
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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

13 authors at 5 institutions in 2 countries.

Yuankun ZhangDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.ORCID 0000-0003-2585-5657
Qingxiao SongArthur Riggs Diabetes & Metabolism Research Institute, City of Hope Medical Center, Duarte, CA 91010.
Kaniel CassadyArthur Riggs Diabetes & Metabolism Research Institute, City of Hope Medical Center, Duarte, CA 91010.
Michael LeeArthur Riggs Diabetes & Metabolism Research Institute, City of Hope Medical Center, Duarte, CA 91010.
Haidong TangDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX 75390.ORCID 0000-0002-1512-2655
Moqian ZhengArthur Riggs Diabetes & Metabolism Research Institute, City of Hope Medical Center, Duarte, CA 91010.
Bixin WangArthur Riggs Diabetes & Metabolism Research Institute, City of Hope Medical Center, Duarte, CA 91010.
Dustin E SchonesArthur Riggs Diabetes & Metabolism Research Institute, City of Hope Medical Center, Duarte, CA 91010.ORCID 0000-0001-7692-8583
Yang-Xin FuDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX 75390.ORCID 0000-0001-8441-6617
Arthur D RiggsArthur Riggs Diabetes & Metabolism Research Institute, City of Hope Medical Center, Duarte, CA 91010.
Paul J MartinFred Hutchinson Cancer Center, Seattle, WA 98109.ORCID 0000-0001-9051-1215
Ru FengDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Defu ZengArthur Riggs Diabetes & Metabolism Research Institute, City of Hope Medical Center, Duarte, CA 91010.
City Of Hope National Medical Center · USFujian Medical University · CNThe University of Texas Southwestern Medical Center · USFred Hutch Cancer Center · USNanfang Hospital · CN

Funding

PD-L1 interacts with CD80 and PD-1 to regulate GVHD and GVL activityR01CA228465 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI ZENG, DEFU · 2018 to 2022
$2.0M
NCI NIH HHS R01 CA228465
6 · The paper itself

Abstract

PD-L1 has two receptors: PD-1 and CD80. Previous reports assumed that PD-L1 and CD80 interacted in trans, but recent reports showed that only cis PD-L1/CD80 interactions existed, and prevention of cis PD-L1/CD80 interactions on antigen-presenting cells (APCs) reduced antitumor immunity via augmenting PD-L1/PD-1 and CD80/CTLA4 interactions between T and APCs. Here, using tumor-bearing mice capable of cis and trans or trans only PD-L1/CD80 interactions, we show that trans PD-L1/CD80 interactions do exist between tumor and T cells, and the effects of trans PD-L1/CD80 interactions require tumor cell expression of MHC-I and T cell expression of CD28. The blockade of PD-L1/CD80 interactions in mice with both cis and trans interactions or with only trans interactions augments antitumor immunity by expanding IFN-γ-producing CD8

Indexed as

B7-H1 AntigenCD8-Positive T-LymphocytesAnimalsB7-1 AntigenCell Adhesion MoleculesLymphocyte ActivationMiceProgrammed Cell Death 1 ReceptorB7-1 AntigenB7-H1 AntigenCell Adhesion MoleculesProgrammed Cell Death 1 ReceptorCD80CD8+ T cellsPD-L1PD-L1 interaction with CD80tumor immunity

Identifiers

PMID37036990
PMCPMC10120074
OpenAlexW4363673745

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.