Evidence map›Paper›PMID 37865779›Full record

ArticleJournal of neuroinflammation2023

Distinguishing the effects of systemic CSF1R inhibition by PLX3397 on microglia and peripheral immune cells.

Akhabue K Okojie, Joseph O Uweru, Morgan A Coburn, Sihan Li, Vivian D Cao-Dao, Ukpong B Eyo

Open access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
6.8field-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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Induced pluripotent stem cell treatment for microglia replacement in progressive MS.Multiple sclerosis (Houndmills, Basingstoke, England) · 2026
    Review
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  9. Microglia Modulate Information Processing in the Mouse Barrel Cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Sunitinib attenuates secondary injury via the regulation of peri-hematomal microglia at the acute phase of intracerebral hemorrhage.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Article
  17. Article
  18. Article
  19. Article
  20. [Effect of removing microglia from spinal cord on nerve repair after spinal cord injury in mice].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2025
    Article
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 1 institution in 1 country.

Akhabue K OkojieDepartment of Neuroscience, University of Virginia School of Medicine, Charlottesville, VA, USA. gsg4pb@virginia.edu.
Joseph O UweruDepartment of Neuroscience, University of Virginia School of Medicine, Charlottesville, VA, USA.
Morgan A CoburnDepartment of Neuroscience, University of Virginia School of Medicine, Charlottesville, VA, USA.
Sihan LiDepartment of Neuroscience, University of Virginia School of Medicine, Charlottesville, VA, USA.
Vivian D Cao-DaoDepartment of Neuroscience, University of Virginia School of Medicine, Charlottesville, VA, USA.
Ukpong B EyoDepartment of Neuroscience, University of Virginia School of Medicine, Charlottesville, VA, USA. ube9q@virginia.edu.
University of Virginia · US

Funding

Targeting Microglia in Febrile Status EpilepticusR01NS119243 · NINDS · UNIVERSITY OF VIRGINIA · PI EYO, UKPONG BASSEY · 2021 to 2025
$2.4M
NIH HHS R01NS119243NINDS NIH HHS R01 NS119243
6 · The paper itself

Abstract

Microglia, the primary immune cells of the central nervous system (CNS), are derived from the yolk sac and populate the brain during development. Once microglia migrate to the CNS, they are self-renewing and require CSF1R signaling for their maintenance. Pexidartinib (PLX3397, PLX), a small molecule inhibitor of the CSF1R, has been shown to effectively deplete microglia since microglial maintenance is CSF1R-dependent. There have, however, been several conflicting reports that have shown the potential off-target effects of PLX on peripheral immune cells particularly those of lymphoid origin. Given this controversy in the use of the PLX family of drugs, it has become important to ascertain to what extent PLX affects the peripheral immune profile in lymphoid (spleen, and bone marrow) and non-lymphoid (kidney, lungs, and heart) organs. PLX3397 chow treatment at 660 mg/kg for 7 days significantly reduced CD45

Indexed as

LipopolysaccharidesMicrogliaAminopyridinesAnimalsMacrophagesMicePyrrolesReceptor Protein-Tyrosine KinasesReceptors, Colony-Stimulating FactorAminopyridinesLipopolysaccharidespexidartinibPyrrolesReceptor Protein-Tyrosine KinasesReceptors, Colony-Stimulating FactorCSF1R inhibitorCytokinesLPSMicrogliaPeripheral immune cellsPLX3397Sickness behavior

Identifiers

PMID37865779
PMCPMC10590528
OpenAlexW4387844370

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.