Evidence map›Paper›PMID 37945822›Full record

ArticleNature immunology2023

CD47 masks pro-phagocytic ligands in cis on tumor cells to suppress antitumor immunity.

Zhenghai Tang, Ming-Chao Zhong, Jin Qian, Cristian Camilo Galindo, Dominique Davidson, Jiaxin Li, Yunlong Zhao, Enfu Hui, André Veillette

Open access · greenAbstract read
In one paragraph

Article in Nature immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
8.4field-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

33 citing papers in PubMed, 51 citations in OpenAlex.

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  17. SLAMF7 promotes TCRαβJournal of experimental & clinical cancer research : CR · 2025
    Article
  18. Article
  19. mCancer cell international · 2025
    Article
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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

9 authors at 2 institutions in 2 countries.

Zhenghai TangLaboratory of Molecular Oncology, Institut de recherches cliniques de Montréal (IRCM), Montréal, Québec, Canada.
Ming-Chao ZhongLaboratory of Molecular Oncology, Institut de recherches cliniques de Montréal (IRCM), Montréal, Québec, Canada.
Jin QianLaboratory of Molecular Oncology, Institut de recherches cliniques de Montréal (IRCM), Montréal, Québec, Canada.
Cristian Camilo GalindoLaboratory of Molecular Oncology, Institut de recherches cliniques de Montréal (IRCM), Montréal, Québec, Canada.ORCID 0000-0003-2344-7756
Dominique DavidsonLaboratory of Molecular Oncology, Institut de recherches cliniques de Montréal (IRCM), Montréal, Québec, Canada.
Jiaxin LiLaboratory of Molecular Oncology, Institut de recherches cliniques de Montréal (IRCM), Montréal, Québec, Canada.
Yunlong ZhaoDepartment of Cell and Developmental Biology, School of Biological Sciences, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0002-7392-4824
Enfu HuiDepartment of Cell and Developmental Biology, School of Biological Sciences, University of California San Diego, La Jolla, CA, USA.
André VeilletteLaboratory of Molecular Oncology, Institut de recherches cliniques de Montréal (IRCM), Montréal, Québec, Canada. andre.veillette@ircm.qc.ca.ORCID 0000-0003-1159-4345
Montreal Clinical Research Institute · CAUniversity of California San Diego · US

Funding

Regulation of PD-L1/PD-1 immune checkpoints by cis-interactionsR37CA239072 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HUI, ENFU · 2019 to 2025
$2.5M
NCI NIH HHS R37 CA239072
6 · The paper itself

Abstract

Cancer cells often overexpress CD47, which triggers the inhibitory receptor SIRPα expressed on macrophages, to elude phagocytosis and antitumor immunity. Pharmacological blockade of CD47 or SIRPα is showing promise as anticancer therapy, although CD47 blockade has been associated with hematological toxicities that may reflect its broad expression pattern on normal cells. Here we found that, in addition to triggering SIRPα, CD47 suppressed phagocytosis by a SIRPα-independent mechanism. This mechanism prevented phagocytosis initiated by the pro-phagocytic ligand, SLAMF7, on tumor cells, due to a cis interaction between CD47 and SLAMF7. The CD47-SLAMF7 interaction was disrupted by CD47 blockade and by a first-in-class agonist SLAMF7 antibody, but not by SIRPα blockade, thereby promoting antitumor immunity. Hence, CD47 suppresses phagocytosis not only by engaging SIRPα, but also by masking cell-intrinsic pro-phagocytic ligands on tumor cells and knowledge of this mechanism may influence the decision between CD47 blockade or SIRPα blockade for therapeutic purposes.

Indexed as

CD47 AntigenNeoplasmsTumor EscapeAnimalsAntigens, DifferentiationHumansLigandsMacrophagesMicePhagocytosisAntigens, DifferentiationCD47 AntigenCD47 protein, humanLigands

Identifiers

PMID37945822
PMCPMC11750626
OpenAlexW4388515908

What OpenQuestion holds

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LicenceTDM
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.