Evidence map›Paper›PMID 29533975›Full record

ReviewInternational journal of molecular sciences2018

The Role of Macrophages in Neuroinflammatory and Neurodegenerative Pathways of Alzheimer's Disease, Amyotrophic Lateral Sclerosis, and Multiple Sclerosis: Pathogenetic Cellular Effectors and Potential Therapeutic Targets.

Santa Mammana, Paolo Fagone, Eugenio Cavalli, Maria Sofia Basile, Maria Cristina Petralia, Ferdinando Nicoletti, Placido Bramanti, Emanuela Mazzon

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed, 3 pooled it
9.2field-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

105 citing papers in PubMed, 3 syntheses or guidelines pooled it, 162 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Article
  6. A FABulous approach to image human macrophages.European journal of nuclear medicine and molecular imaging · 2026
    Article
  7. Review
  8. Review
  9. Article
  10. Phenolic-Enriched Fractions ofCurrent issues in molecular biology · 2026
    Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Unmasking a Paradox: Roles of the PD-1/PD-L1 Axis in Alzheimer's Disease-Associated Neuroinflammation.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2025
    Review
  18. Review
  19. Review
  20. Review

45 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.

Santa MammanaDepartment of Biomedical and Biotechnological Sciences, University of Catania, 95123 Catania, Italy. santa84ma@libero.it.
Paolo FagoneDepartment of Biomedical and Biotechnological Sciences, University of Catania, 95123 Catania, Italy. paolofagone@yahoo.it.
Eugenio CavalliDepartment of Biomedical and Biotechnological Sciences, University of Catania, 95123 Catania, Italy. eugeniocavalli9@hotmail.it.
Maria Sofia BasileDepartment of Biomedical and Biotechnological Sciences, University of Catania, 95123 Catania, Italy. sofiabasile@hotmail.it.
Maria Cristina PetraliaDepartment of Biomedical and Biotechnological Sciences, University of Catania, 95123 Catania, Italy. m.cristinapetralia@gmail.com.
Ferdinando NicolettiDepartment of Biomedical and Biotechnological Sciences, University of Catania, 95123 Catania, Italy. ferdinic@unict.it.
Placido BramantiIRCCS Centro Neurolesi "Bonino-Pulejo", 98124 Messina, Italy. bramanti.dino@gmail.com.
Emanuela MazzonIRCCS Centro Neurolesi "Bonino-Pulejo", 98124 Messina, Italy. emazzon.irccs@gmail.com.ORCID 0000-0002-5073-717X
University of Catania · ITCentro Neurolesi Bonino Pulejo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In physiological conditions, different types of macrophages can be found within the central nervous system (CNS), i.e., microglia, meningeal macrophages, and perivascular (blood-brain barrier) and choroid plexus (blood-cerebrospinal fluid barrier) macrophages. Microglia and tissue-resident macrophages, as well as blood-borne monocytes, have different origins, as the former derive from yolk sac erythromyeloid precursors and the latter from the fetal liver or bone marrow. Accordingly, specific phenotypic patterns characterize each population. These cells function to maintain homeostasis and are directly involved in the development and resolution of neuroinflammatory processes. Also, following inflammation, circulating monocytes can be recruited and enter the CNS, therefore contributing to brain pathology. These cell populations have now been identified as key players in CNS pathology, including autoimmune diseases, such as multiple sclerosis, and degenerative diseases, such as Amyotrophic Lateral Sclerosis and Alzheimer's disease. Here, we review the evidence on the involvement of CNS macrophages in neuroinflammation and the advantages, pitfalls, and translational opportunities of pharmacological interventions targeting these heterogeneous cellular populations for the treatment of brain diseases.

Indexed as

Alzheimer DiseaseAmyotrophic Lateral SclerosisAnimalsCentral Nervous SystemHumansMacrophagesMolecular Targeted TherapyMultiple SclerosisAlzheimer’s diseaseAmyotrophic Lateral Sclerosismacrophagesmicrogliamultiple sclerosisneuroinflammation

Identifiers

PMID29533975
PMCPMC5877692
OpenAlexW2790994161

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.