Evidence map›Paper›PMID 30769926›Full record

ReviewInternational journal of molecular sciences2019

Innate Immune Modulation by GM-CSF and IL-3 in Health and Disease.

Francesco Borriello, Maria Rosaria Galdiero, Gilda Varricchi, Stefania Loffredo, Giuseppe Spadaro, Gianni Marone

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 80 citations in OpenAlex.

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  18. Basophils from allergy to cancer.Frontiers in immunology · 2022
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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

6 authors at 3 institutions in 2 countries.

Francesco BorrielloDivision of Gastroenterology, Boston Children's Hospital and Harvard Medical School, Boston, MA 02115, USA. francesco.borriello@childrens.harvard.edu.
Maria Rosaria GaldieroDepartment of Translational Medical Sciences and Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, 80131 Naples, Italy. mrgaldiero@libero.it.
Gilda VarricchiDepartment of Translational Medical Sciences and Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, 80131 Naples, Italy. gildanet@gmail.com.ORCID 0000-0002-9285-4657
Stefania LoffredoDepartment of Translational Medical Sciences and Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, 80131 Naples, Italy. stefanialoffredo@hotmail.com.
Giuseppe SpadaroDepartment of Translational Medical Sciences and Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, 80131 Naples, Italy. spadaro@unina.it.
Gianni MaroneDepartment of Translational Medical Sciences and Center for Basic and Clinical Immunology Research (CISI), University of Naples Federico II, 80131 Naples, Italy. marone@unina.it.ORCID 0000-0002-9849-4701
University of Naples Federico II · ITBoston Children's Hospital · USInstitute for Experimental Endocrinology and Oncology · IT

Funding

Regione Campania CISI-Lab ProjectRegione Campania TIMING Project
6 · The paper itself

Abstract

Granulocyte-macrophage colony-stimulating factor (GM-CSF) and inteleukin-3 (IL-3) have long been known as mediators of emergency myelopoiesis, but recent evidence has highlighted their critical role in modulating innate immune effector functions in mice and humans. This new wealth of knowledge has uncovered novel aspects of the pathogenesis of a range of disorders, including infectious, neoplastic, autoimmune, allergic and cardiovascular diseases. Consequently, GM-CSF and IL-3 are now being investigated as therapeutic targets for some of these disorders, and some phase I/II clinical trials are already showing promising results. There is also pre-clinical and clinical evidence that GM-CSF can be an effective immunostimulatory agent when being combined with anti-cytotoxic T lymphocyte-associated protein 4 (anti-CTLA-4) in patients with metastatic melanoma as well as in novel cancer immunotherapy approaches. Finally, GM-CSF and to a lesser extent IL-3 play a critical role in experimental models of trained immunity by acting not only on bone marrow precursors but also directly on mature myeloid cells. Altogether, characterizing GM-CSF and IL-3 as central mediators of innate immune activation is poised to open new therapeutic avenues for several immune-mediated disorders and define their potential in the context of immunotherapies.

Indexed as

AnimalsCTLA-4 AntigenGranulocyte-Macrophage Colony-Stimulating FactorHumansImmunity, InnateImmunotherapyInterleukin-3MelanomaMiceCTLA-4 AntigenGranulocyte-Macrophage Colony-Stimulating FactorInterleukin-3allergyatherosclerosiscancer immunotherapyexperimental autoimmune encephalomyelitisGM-CSFIL-3inflammatory bowel diseasesinnate immunityrheumatoid arthritissepsistrained immunity

Identifiers

PMID30769926
PMCPMC6412223
OpenAlexW2914822143

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.