Evidence map›Paper›PMID 32294445›Full record

ArticleCell reports2020

Immunotherapeutic Blockade of CD47 Inhibitory Signaling Enhances Innate and Adaptive Immune Responses to Viral Infection.

Lamin B Cham, Laughing Bear Torrez Dulgeroff, Michal Caspi Tal, Tom Adomati, Fanghui Li, Hilal Bhat, Anfei Huang, Philipp A Lang, Mary E Moreno, Jose M Rivera and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Review
  3. CD47 monoclonal antibodies differ in their capacity to induce immune response.European journal of microbiology & immunology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Beyond resorption: osteoclasts as drivers of bone formation.Cell regeneration (London, England) · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Phagocytic cooperativity by tumour macrophages.Nature biomedical engineering · 2023
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review
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 5 institutions in 2 countries.

Lamin B ChamInstitute of Immunology, Medical Faculty, University of Duisburg-Essen, Hufelandstrasse 55, 45147 Essen, Germany.
Laughing Bear Torrez DulgeroffInstitute for Stem Cell Biology and Regenerative Medicine, and Ludwig Center for Cancer Stem Cell Research, Stanford University School of Medicine, Stanford, CA 94305, USA.
Michal Caspi TalInstitute for Stem Cell Biology and Regenerative Medicine, and Ludwig Center for Cancer Stem Cell Research, Stanford University School of Medicine, Stanford, CA 94305, USA.
Tom AdomatiInstitute of Immunology, Medical Faculty, University of Duisburg-Essen, Hufelandstrasse 55, 45147 Essen, Germany.
Fanghui LiInstitute of Immunology, Medical Faculty, University of Duisburg-Essen, Hufelandstrasse 55, 45147 Essen, Germany.
Hilal BhatInstitute of Immunology, Medical Faculty, University of Duisburg-Essen, Hufelandstrasse 55, 45147 Essen, Germany.
Anfei HuangDepartment of Molecular Medicine II, Medical Faculty, Heinrich Heine University, 40225 Dusseldorf, Germany.
Philipp A LangDepartment of Molecular Medicine II, Medical Faculty, Heinrich Heine University, 40225 Dusseldorf, Germany.
Mary E MorenoDepartment of Medicine, Division of Experimental Medicine, University of California, San Francisco, CA 94110, USA.
Jose M RiveraDepartment of Medicine, Division of Experimental Medicine, University of California, San Francisco, CA 94110, USA.
Sofiya A GalkinaDepartment of Medicine, Division of Experimental Medicine, University of California, San Francisco, CA 94110, USA.
Galina KosikovaDepartment of Medicine, Division of Experimental Medicine, University of California, San Francisco, CA 94110, USA.
Cheryl A StoddartDepartment of Medicine, Division of Experimental Medicine, University of California, San Francisco, CA 94110, USA.
Joseph M McCuneDepartment of Medicine, Division of Experimental Medicine, University of California, San Francisco, CA 94110, USA.
Lara M MyersLaboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, NIAID, NIH, Hamilton, MT 59840, USA.
Irving L WeissmanInstitute for Stem Cell Biology and Regenerative Medicine, and Ludwig Center for Cancer Stem Cell Research, Stanford University School of Medicine, Stanford, CA 94305, USA.
Karl S LangInstitute of Immunology, Medical Faculty, University of Duisburg-Essen, Hufelandstrasse 55, 45147 Essen, Germany. Electronic address: karlsebastian.lang@uk-essen.de.
Kim J HasenkrugLaboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, NIAID, NIH, Hamilton, MT 59840, USA. Electronic address: khasenkrug@nih.gov.
University of California, San Francisco · USUniversity of Duisburg-Essen · DECalifornia Institute for Regenerative Medicine · USHeinrich Heine University Düsseldorf · DERocky Mountain Research (United States) · US

Funding

MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
Immunology And Pathology Of Acute Murine Leukemia Virus InfectionsZIAAI000753 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI HASENKRUG, KIM · 2009 to 2022
$8.1M
SARS-CoV-2 Immunology and TherapeuticsZIAAI001277 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI HASENKRUG, KIM · 2020 to 2022
$109k
Immunotherapy targeting the CD47-SIRPα axis to promote immune clearance of chronic infectionF32AI124558 · NIAID · STANFORD UNIVERSITY · PI TAL, MICHAL CASPI · 2016 to 2017
$83k
Intramural NIH HHS ZIA AI000753NIAID NIH HHS F32 AI124558NIAID NIH HHS HHSN266200700005CNIAID NIH HHS N01 AI070002NIAID NIH HHS T32 AI007290
6 · The paper itself

Abstract

Paradoxically, early host responses to infection include the upregulation of the antiphagocytic molecule, CD47. This suggests that CD47 blockade could enhance antigen presentation and subsequent immune responses. Indeed, mice treated with anti-CD47 monoclonal antibody following lymphocytic choriomeningitis virus infections show increased activation of both macrophages and dendritic cells (DCs), enhancement of the kinetics and potency of CD8

Indexed as

Adaptive ImmunityAnimalsCD47 AntigenCD8-Positive T-LymphocytesCell LineFemaleHEK293 CellsHumansImmunity, InnateImmunotherapyLymphocytic ChoriomeningitisLymphocytic choriomeningitis virusMacrophagesMice, Inbred C57BLMice, KnockoutSignal TransductionCD47 AntigenCD47 protein, humanadaptive immunityCD47checkpoint inhibitorsdendritic cellsHIV-1innate immunityLCMV

Identifiers

PMID32294445
PMCPMC8369894
OpenAlexW3015969228

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.