Evidence map›Paper›PMID 35122038›Full record

ArticleNature cancer2020

PD-L1 expression by dendritic cells is a key regulator of T-cell immunity in cancer.

Soyoung A Oh, Dai-Chen Wu, Jeanne Cheung, Armando Navarro, Huizhong Xiong, Rafael Cubas, Klara Totpal, Henry Chiu, Yan Wu, Laetitia Comps-Agrar and 8 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 305 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
305citing papers in PubMed, 2 pooled it
19.2field-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

305 citing papers in PubMed, 2 syntheses or guidelines pooled it, 449 citations in OpenAlex.

  1. Pooled it
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  11. Review
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  13. Dendritic cell PD-L2 restrains intratumoral CD8bioRxiv : the preprint server for biology · 2026
    Article
  14. Article
  15. Sequential Immune Activation of Effector T Cells as Biomarkers of Response to Durvalumab in Patients with Locally Advanced NSCLC.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Observational
  16. Article
  17. Article
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  19. Tumor-Infiltrating mregDCs Restrain Anti-Tumor Immunity in Early Relapse HCC.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  20. Article

245 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

18 authors at 4 institutions in 1 country.

Soyoung A OhGenentech, Inc., South San Francisco, CA, USA.
Dai-Chen WuGenentech, Inc., South San Francisco, CA, USA.ORCID http://orcid.org/0000-0003-3327-4887
Jeanne CheungGenentech, Inc., South San Francisco, CA, USA.
Armando NavarroGenentech, Inc., South San Francisco, CA, USA.
Huizhong XiongGenentech, Inc., South San Francisco, CA, USA.
Rafael CubasGenentech, Inc., South San Francisco, CA, USA.
Klara TotpalGenentech, Inc., South San Francisco, CA, USA.
Henry ChiuGenentech, Inc., South San Francisco, CA, USA.
Yan WuGenentech, Inc., South San Francisco, CA, USA.
Laetitia Comps-AgrarGenentech, Inc., South San Francisco, CA, USA.
Andrew M LeaderDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Miriam MeradDepartment of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Merone Roose-GermaGenentech, Inc., South San Francisco, CA, USA.
Soren WarmingGenentech, Inc., South San Francisco, CA, USA.
Minhong YanGenentech, Inc., South San Francisco, CA, USA.ORCID http://orcid.org/0000-0001-6126-9714
Jeong M KimGenentech, Inc., South San Francisco, CA, USA.
Sascha RutzGenentech, Inc., South San Francisco, CA, USA.
Ira MellmanGenentech, Inc., South San Francisco, CA, USA. mellman.ira@gene.com.ORCID http://orcid.org/0000-0002-6132-7299
Icahn School of Medicine at Mount Sinai · USGenesys (United States) · USNGM Biopharmaceuticals (United States) · USRedwood Scientific (United States) · US

Funding

TRAINING PROGRAM IN CANCER THERAPYT32CA078207 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI James J Manfredi · 1999 to 2026
$11.6M
Novel tools to maximize profiling of tissue and antigen specific immune dysregulation in allergy and inflammatory bowel disesaseU24AI118644 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BERIN, CECILIA, MERAD, MIRIAM · 2015 to 2020
$2.4M
Harnessing Csf-2 compartmentalized role on tissue resident phagocytes to uncouple anti-tumoral from pathological immunity induced by checkpoint inhibitorsR01CA190400 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MERAD, MIRIAM · 2015 to 2019
$1.9M
NCI NIH HHS R01 CA190400NCI NIH HHS T32 CA078207NIAID NIH HHS U24 AI118644
6 · The paper itself

Abstract

Inhibiting the programmed death-1 (PD-1) pathway is one of the most effective approaches to cancer immunotherapy, but its mechanistic basis remains incompletely understood. Binding of PD-1 to its ligand PD-L1 suppresses T-cell function in part by inhibiting CD28 signaling. Tumor cells and infiltrating myeloid cells can express PD-L1, with myeloid cells being of particular interest as they also express B7-1, a ligand for CD28 and PD-L1. Here we demonstrate that dendritic cells (DCs) represent a critical source of PD-L1, despite being vastly outnumbered by PD-L1

Indexed as

B7-H1 AntigenNeoplasmsCD28 AntigensDendritic CellsHumansLigandsProgrammed Cell Death 1 ReceptorB7-H1 AntigenCD28 AntigensLigandsProgrammed Cell Death 1 Receptor

Identifiers

PMID35122038
OpenAlexW3036599100

What OpenQuestion holds

Textmetadata
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.