Evidence map›Paper›PMID 26322579›Full record

ArticleNature medicine2015

CD47 blockade triggers T cell-mediated destruction of immunogenic tumors.

Xiaojuan Liu, Yang Pu, Kyle Cron, Liufu Deng, Justin Kline, William A Frazier, Hairong Xu, Hua Peng, Yang-Xin Fu, Meng Michelle Xu

Open access · greenAbstract read
In one paragraph

Article in Nature medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 476 papers.

0numbers the graph read from it
0cells of the map it votes in
476citing papers in PubMed
21.0field-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

476 citing papers in PubMed, 745 citations in OpenAlex.

  1. Trial
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  11. Article
  12. CD47 and FOXP3Cancers · 2026
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Immune checkpoints in lung cancer.Breathe (Sheffield, England) · 2026
    Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 2 countries.

Xiaojuan LiuInstitute of Biophysics and the University of Chicago Joint Group for Immunotherapy, Chinese Academy of Science Key Laboratory for Infection and Immunity, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Yang PuDepartment of Pathology and Committee on Immunology, University of Chicago, Chicago, Illinois, USA.
Kyle CronDepartment of Pathology and Committee on Immunology, University of Chicago, Chicago, Illinois, USA.
Liufu DengDepartment of Pathology and Committee on Immunology, University of Chicago, Chicago, Illinois, USA.
Justin KlineDepartment of Medicine and Committee on Immunology, University of Chicago, Chicago, Illinois, USA.
William A FrazierDepartment of Biochemistry and Molecular Biophysics, Washington University, St. Louis, Missouri, USA.
Hairong XuInstitute of Biophysics and the University of Chicago Joint Group for Immunotherapy, Chinese Academy of Science Key Laboratory for Infection and Immunity, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Hua PengInstitute of Biophysics and the University of Chicago Joint Group for Immunotherapy, Chinese Academy of Science Key Laboratory for Infection and Immunity, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Yang-Xin FuInstitute of Biophysics and the University of Chicago Joint Group for Immunotherapy, Chinese Academy of Science Key Laboratory for Infection and Immunity, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Meng Michelle XuDepartment of Pathology and Committee on Immunology, University of Chicago, Chicago, Illinois, USA.
University of Chicago · USInstitute of Biophysics · CNChinese Academy of Sciences · CNUniversity of Chinese Academy of Sciences · CNWashington University in St. Louis · US

Funding

INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGYT32AI007090 · NIAID · UNIVERSITY OF CHICAGO · PI Peter Aidan Savage · 1985 to 2026
$11.7M
Synergy of Radiation and Immunotherapy: New ApproachesR01CA134563 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MALTER, JAMES S · 2010 to 2019
$3.4M
Characterization of a T cell dysfunctional state induced in mice with AMLR01CA166770 · NCI · UNIVERSITY OF CHICAGO · PI KLINE, JUSTIN P. · 2012 to 2016
$1.6M
TNF family members for lymph angiogenesis and lymph node hypertrophyR01CA141975 · NCI · UNIVERSITY OF CHICAGO · PI FU, YANG-XIN · 2010 to 2014
$1.6M
NCI NIH HHS CA134563NCI NIH HHS CA141975NCI NIH HHS R01 CA134563NCI NIH HHS R01 CA141975NCI NIH HHS R01 CA166770NIAID NIH HHS T32 AI007090
6 · The paper itself

Abstract

Macrophage phagocytosis of tumor cells mediated by CD47-specific blocking antibodies has been proposed to be the major effector mechanism in xenograft models. Here, using syngeneic immunocompetent mouse tumor models, we reveal that the therapeutic effects of CD47 blockade depend on dendritic cell but not macrophage cross-priming of T cell responses. The therapeutic effects of anti-CD47 antibody therapy were abrogated in T cell-deficient mice. In addition, the antitumor effects of CD47 blockade required expression of the cytosolic DNA sensor STING, but neither MyD88 nor TRIF, in CD11c+ cells, suggesting that cytosolic sensing of DNA from tumor cells is enhanced by anti-CD47 treatment, further bridging the innate and adaptive responses. Notably, the timing of administration of standard chemotherapy markedly impacted the induction of antitumor T cell responses by CD47 blockade. Together, our findings indicate that CD47 blockade drives T cell-mediated elimination of immunogenic tumors.

Indexed as

ImmunotherapyAnimalsAntineoplastic AgentsCD47 AntigenDNAHumansMiceMice, Inbred BALB CNeoplasmsT-LymphocytesXenograft Model Antitumor AssaysAntineoplastic AgentsCD47 AntigenCD47 protein, humanDNA

Identifiers

PMID26322579
PMCPMC4598283
OpenAlexW2133346943

What OpenQuestion holds

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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.