Evidence map›Paper›PMID 35366105›Full record

ReviewCellular and molecular life sciences : CMLS2022

Inhibition of colony stimulating factor-1 receptor (CSF-1R) as a potential therapeutic strategy for neurodegenerative diseases: opportunities and challenges.

Jinming Han, Violeta Chitu, E Richard Stanley, Zbigniew K Wszolek, Virginija Danylaité Karrenbauer, Robert A Harris

Open access · hybridAbstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 1 pooled it
11.6field-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

60 citing papers in PubMed, 1 synthesis or guideline pooled it, 147 citations in OpenAlex.

  1. Pooled it
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  16. Modulation of macrophage survival duringFrontiers in cellular and infection microbiology · 2026
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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 4 institutions in 3 countries.

Jinming HanDepartment of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Violeta ChituDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
E Richard StanleyDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Zbigniew K WszolekDepartment of Neurology, Mayo Clinic, Jacksonville, USA.
Virginija Danylaité Karrenbauer *Department of Clinical Neuroscience, Center for Molecular Medicine L8:04, Karolinska Institutet, Karolinska University Hospital, 171 76, Stockholm, Sweden. virginija.karrenbauer@ki.se.ORCID http://orcid.org/0000-0002-7166-8951
Robert A Harris *Applied Immunology and Immunotherapy, Department of Clinical Neuroscience, Center for Molecular Medicine, Karolinska Institutet, Karolinska University Hospital, Solna, Sweden. robert.harris@ki.se.
Albert Einstein College of Medicine · USKarolinska University Hospital · SECapital Medical University · CNWinnMed · US

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI Ulrich Steidl · 1985 to 2026
$111.2M
Support for the Rose F. Kennedy IDDRCU54HD090260 · NICHD · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI SCHWARTZ, GARY J · 2016 to 2020
$6.0M
Analysis of a mouse model of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia.R01NS091519 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI STANLEY, E. RICHARD · 2015 to 2019
$2.5M
Foundation for the National Institutes of Health Grant R01NS091519Intellectual and Developmental Disabilities Research Center U54 HD090260 support for the Rose F. KennedyNCI NIH HHS P30 CA013330NCI NIH HHS P30CA013330NCI NIH HHS P30CA013330 NCI Cancer Center GrantNICHD NIH HHS U54 HD090260NINDS NIH HHS R01 NS091519
6 · The paper itself

Abstract

Microglia are specialized dynamic immune cells in the central nervous system (CNS) that plays a crucial role in brain homeostasis and in disease states. Persistent neuroinflammation is considered a hallmark of many neurodegenerative diseases, including Alzheimer's disease (AD), Parkinson's disease (PD), Huntington's disease (HD), amyotrophic lateral sclerosis (ALS) and primary progressive multiple sclerosis (MS). Colony stimulating factor 1-receptor (CSF-1R) is predominantly expressed on microglia and its expression is significantly increased in neurodegenerative diseases. Cumulative findings have indicated that CSF-1R inhibitors can have beneficial effects in preclinical neurodegenerative disease models. Research using CSF-1R inhibitors has now been extended into non-human primates and humans. This review article summarizes the most recent advances using CSF-1R inhibitors in different neurodegenerative conditions including AD, PD, HD, ALS and MS. Potential challenges for translating these findings into clinical practice are presented.

Indexed as

Alzheimer DiseaseNeurodegenerative DiseasesParkinson DiseaseAnimalsColony-Stimulating FactorsMicrogliaColony-Stimulating FactorsAlzheimer’s diseaseAmyotrophic lateral sclerosisColony stimulating factor-1 receptorHuntington’s diseaseMultiple sclerosisParkinson’s disease

Identifiers

PMID35366105
PMCPMC8976111
OpenAlexW4225006102

What Socratic 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 Socratic graph.