Evidence map›Paper›PMID 25803788›Full record

ReviewJournal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research2015

Dual Role of GM-CSF as a Pro-Inflammatory and a Regulatory Cytokine: Implications for Immune Therapy.

Palash Bhattacharya, Isadore Budnick, Medha Singh, Muthusamy Thiruppathi, Khaled Alharshawi, Hatem Elshabrawy, Mark J Holterman, Bellur S Prabhakar

Abstract readReview
In one paragraph

Review in Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 175 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
175citing papers in PubMed, 1 pooled it
8.6field-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

175 citing papers in PubMed, 1 synthesis or guideline pooled it, 253 citations in OpenAlex.

  1. Pooled it
  2. mBio · 2026
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  13. Frontiers in immunology · 2026
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  19. Observational
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115 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

8 authors at 2 institutions in 1 country.

Palash Bhattacharya1 Department of Microbiology and Immunology, College of Medicine, University of Illinois , Chicago, Illinois.
Isadore Budnick1 Department of Microbiology and Immunology, College of Medicine, University of Illinois , Chicago, Illinois.
Medha Singh1 Department of Microbiology and Immunology, College of Medicine, University of Illinois , Chicago, Illinois.
Muthusamy Thiruppathi1 Department of Microbiology and Immunology, College of Medicine, University of Illinois , Chicago, Illinois.
Khaled Alharshawi1 Department of Microbiology and Immunology, College of Medicine, University of Illinois , Chicago, Illinois.
Hatem Elshabrawy1 Department of Microbiology and Immunology, College of Medicine, University of Illinois , Chicago, Illinois.
Mark J Holterman2 Department of Surgery, College of Medicine, University of Illinois , Chicago, Illinois.
Bellur S Prabhakar1 Department of Microbiology and Immunology, College of Medicine, University of Illinois , Chicago, Illinois.
University of Illinois Chicago · USUniversity of Illinois Urbana-Champaign · US

Funding

G-BMDC-induced Treg mediated suppression of Type 1 Diabetes in NOD miceR01AI107516 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PRABHAKAR, BELLUR S · 2014 to 2017
$1.6M
Use of Bispecific Antibody for Treating Non-obese DiabetesR41AI085677 · NIAID · TOLEROGENICS, INC. · PI PRABHAKAR, BELLUR S · 2011 to 2011
$193k
NIAID NIH HHS 1R41AI085677-01NIAID NIH HHS R01 AI107516NIAID NIH HHS R01 AI107516-01A1
6 · The paper itself

Abstract

Granulocyte macrophage colony stimulating factor (GM-CSF) is generally recognized as an inflammatory cytokine. Its inflammatory activity is primarily due its role as a growth and differentiation factor for granulocyte and macrophage populations. In this capacity, among other clinical applications, it has been used to bolster anti-tumor immune responses. GM-CSF-mediated inflammation has also been implicated in certain types of autoimmune diseases, including rheumatoid arthritis and multiple sclerosis. Thus, agents that can block GM-CSF or its receptor have been used as anti-inflammatory therapies. However, a review of literature reveals that in many situations GM-CSF can act as an anti-inflammatory/regulatory cytokine. We and others have shown that GM-CSF can modulate dendritic cell differentiation to render them "tolerogenic," which, in turn, can increase regulatory T-cell numbers and function. Therefore, the pro-inflammatory and regulatory effects of GM-CSF appear to depend on the dose and the presence of other relevant cytokines in the context of an immune response. A thorough understanding of the various immunomodulatory effects of GM-CSF will facilitate more appropriate use and thus further enhance its clinical utility.

Indexed as

AnimalsAnti-Inflammatory AgentsAutoimmune DiseasesAutoimmunityCytokinesDrug Evaluation, PreclinicalGranulocyte-Macrophage Colony-Stimulating FactorHumansImmune ToleranceImmunosuppressive AgentsImmunotherapyInflammationInflammation MediatorsAnti-Inflammatory AgentsCytokinesGranulocyte-Macrophage Colony-Stimulating FactorImmunosuppressive AgentsInflammation Mediators

Identifiers

PMID25803788
PMCPMC4529096
OpenAlexW2322706669

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.