Evidence map›Paper›PMID 39719687›Full record

ReviewGlia2025

Microglial Depletion, a New Tool in Neuroinflammatory Disorders: Comparison of Pharmacological Inhibitors of the CSF-1R.

David Guenoun, Nathan Blaise, Alexandre Sellam, Julie Roupret-Serzec, Alice Jacquens, Juliette Van Steenwinckel, Pierre Gressens, Cindy Bokobza

Abstract readReviewComparative Study
In one paragraph

Review in Glia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

18 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. The neuroimmune-glutamate hypothesis of addiction.Neuroscience and biobehavioral reviews · 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

8 authors.

David GuenounInserm, NeuroDiderot, Université Paris-Cité, Paris, France.ORCID 0000-0001-8377-4703
Nathan BlaiseInserm, NeuroDiderot, Université Paris-Cité, Paris, France.
Alexandre SellamInserm, NeuroDiderot, Université Paris-Cité, Paris, France.
Julie Roupret-SerzecDepartment of Pharmacy, Robert Debré Hospital (AP-HP), Paris, France.
Alice JacquensInserm, NeuroDiderot, Université Paris-Cité, Paris, France.ORCID 0000-0002-9241-6884
Juliette Van SteenwinckelInserm, NeuroDiderot, Université Paris-Cité, Paris, France.ORCID 0000-0003-3463-4856
Pierre GressensInserm, NeuroDiderot, Université Paris-Cité, Paris, France.ORCID 0000-0002-0909-4221
Cindy BokobzaInserm, NeuroDiderot, Université Paris-Cité, Paris, France.ORCID 0000-0003-0992-4317

Funding

Agence Nationale de la Recherche ANR-22-CE37-0019Agence Nationale de la Recherche Investissement d'Avenir-ANR-11-INBS-0011-NeurATRAssistance Publique - Hôpitaux de ParisFondation de FranceFondation des Gueules CasséesHorizon 2020 Framework Programme PREMSTEM-874721Institut National de la Santé et de la Recherche MédicaleUniversité Sorbonne Paris Cité
6 · The paper itself

Abstract

A growing body of evidence highlights the importance of microglia, the resident immune cells of the CNS, and their pro-inflammatory activation in the onset of many neurological diseases. Microglial proliferation, differentiation, and survival are highly dependent on the CSF-1 signaling pathway, which can be pharmacologically modulated by inhibiting its receptor, CSF-1R. Pharmacological inhibition of CSF-1R leads to an almost complete microglial depletion whereas treatment arrest allows for subsequent repopulation. Microglial depletion has shown promising results in many animal models of neurodegenerative diseases (Alzheimer's disease (AD), Parkinson's disease, or multiple sclerosis) where transitory microglial depletion reduced neuroinflammation and improved behavioral test results. In this review, we will focus on the comparison of three different pharmacological CSF-1R inhibitors (PLX3397, PLX5622, and GW2580) regarding microglial depletion. We will also highlight the promising results obtained by microglial depletion strategies in adult models of neurological disorders and argue they could also prove promising in neurodevelopmental diseases associated with microglial activation and neuroinflammation. Finally, we will discuss the lack of knowledge about the effects of these strategies on neurons, astrocytes, and oligodendrocytes in adults and during neurodevelopment.

Indexed as

MicrogliaNeuroinflammatory DiseasesReceptors, Granulocyte-Macrophage Colony-Stimulating FactorAminopyridinesAnimalsAnisolesHumansNeurodegenerative DiseasesOrganic ChemicalsPyrimidinesPyrrolesSulfonamides5-(3-methoxy-4-((4-methoxybenzyl)oxy)benzyl)pyrimidine-2,4-diamineAminopyridinesAnisolesOrganic ChemicalspexidartinibPLX5622PyrimidinesPyrrolesReceptors, Granulocyte-Macrophage Colony-Stimulating FactorSulfonamidesCSF‐1CSF‐1RdepletionGW2580microglianeurologyPLX3397PLX5622

Identifiers

PMID39719687
PMCPMC11845850

What OpenQuestion holds

Textmetadata
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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.