Evidence map›Paper›PMID 26441984›Full record

ReviewFrontiers in immunology2015

Splenic Macrophage Subsets and Their Function during Blood-Borne Infections.

Henrique Borges da Silva, Raíssa Fonseca, Rosana Moreira Pereira, Alexandra Dos Anjos Cassado, José Maria Álvarez, Maria Regina D'Império Lima

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 113 papers.

0numbers the graph read from it
0cells of the map it votes in
113citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

113 citing papers in PubMed, 198 citations in OpenAlex.

  1. Article
  2. Review
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  7. Review
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  9. Review
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  12. Loss of NR2F6 Protects from Salmonella Typhimurium Infection.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  13. Article
  14. Review
  15. Exploring CD169Vaccines · 2025
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

53 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

6 authors at 1 institution in 1 country.

Henrique Borges da SilvaDepartment of Immunology, Instituto de Ciências Biomédicas, Universidade de São Paulo , São Paulo , Brazil.
Raíssa FonsecaDepartment of Immunology, Instituto de Ciências Biomédicas, Universidade de São Paulo , São Paulo , Brazil.
Rosana Moreira PereiraDepartment of Immunology, Instituto de Ciências Biomédicas, Universidade de São Paulo , São Paulo , Brazil.
Alexandra Dos Anjos CassadoDepartment of Immunology, Instituto de Ciências Biomédicas, Universidade de São Paulo , São Paulo , Brazil.
José Maria ÁlvarezDepartment of Immunology, Instituto de Ciências Biomédicas, Universidade de São Paulo , São Paulo , Brazil.
Maria Regina D'Império LimaDepartment of Immunology, Instituto de Ciências Biomédicas, Universidade de São Paulo , São Paulo , Brazil.
Universidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The spleen is one of the major immunological sites for maintaining blood homeostasis. Previous studies showed that heterogeneous splenic macrophage populations contribute in complimentary ways to control blood-borne infections and induce effective immune responses. Marginal metallophilic macrophages (MMMΦs) and marginal zone macrophages (MZMΦs) are cells with great ability to internalize blood-borne pathogens such as virus or bacteria. Their localization adjacent to T- and B-cell-rich splenic areas favors the rapid contact between these macrophages and cells from adaptive immunity. Indeed, MMMΦs and MZMΦs are considered important bridges between innate and adaptive immunity. Although red pulp macrophages (RpMΦs) are mainly considered scavengers for senescent erythrocytes, several data indicate a role for RpMΦs in control of infections such as blood-stage malaria as well as in the induction of innate and adaptive immunity. Here, we review current data on how different macrophage subsets recognize and help eliminate blood-borne pathogens, and, in turn, how the inflammatory microenvironment in different phases of infection (acute, chronic, and after pathogen clearance) influences macrophage function and survival.

Indexed as

macrophagespattern-recognition receptorsphagocytosisspleentissue remodeling

Identifiers

PMID26441984
PMCPMC4585205
OpenAlexW1444346221

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.