Evidence map›Paper›PMID 33112414›Full record

ArticleImmunology2021

Selective serotonin reuptake inhibitor attenuates the hyperresponsiveness of TLR2

Marisa C Sales, Taissa M Kasahara, Priscila M Sacramento, Átila D Rossi, Marcos Octávio S D Cafasso, Hugo A A Oyamada, Joana Hygino, Fabianna Alvim, Regis M Andrade, Cláudia Cristina Vasconcelos and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.1field-weighted citation impact, top 28% 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

21 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. The emerging role of T cells in depression.Frontiers in psychiatry · 2026
    Review
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  8. Depression and anxiety in multiple sclerosis. Review of a fatal combination.Journal of neural transmission (Vienna, Austria : 1996) · 2024
    Review
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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

11 authors at 3 institutions in 1 country.

Marisa C SalesDepartment of Microbiology and Parasitology, Federal University of the State of Rio de Janeiro, Rio de Janeiro, Brazil.
Taissa M KasaharaDepartment of Microbiology and Parasitology, Federal University of the State of Rio de Janeiro, Rio de Janeiro, Brazil.ORCID 0000-0002-1366-1049
Priscila M SacramentoDepartment of Microbiology and Parasitology, Federal University of the State of Rio de Janeiro, Rio de Janeiro, Brazil.
Átila D RossiDepartment of Genetics, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Marcos Octávio S D CafassoDepartment of Microbiology and Parasitology, Federal University of the State of Rio de Janeiro, Rio de Janeiro, Brazil.
Hugo A A OyamadaDepartment of Microbiology and Parasitology, Federal University of the State of Rio de Janeiro, Rio de Janeiro, Brazil.ORCID 0000-0002-4518-2018
Joana HyginoDepartment of Microbiology and Parasitology, Federal University of the State of Rio de Janeiro, Rio de Janeiro, Brazil.
Fabianna AlvimDepartment of Microbiology and Parasitology, Federal University of the State of Rio de Janeiro, Rio de Janeiro, Brazil.
Regis M AndradeDepartment of General Medicine Department, Federal University of the State of Rio de Janeiro, Rio de Janeiro, Brazil.
Cláudia Cristina VasconcelosPost-graduate Program in Neurology, Federal University of the State of Rio de Janeiro, Rio de Janeiro, Brazil.
Cleonice A M BentoDepartment of Microbiology and Parasitology, Federal University of the State of Rio de Janeiro, Rio de Janeiro, Brazil.ORCID 0000-0002-8613-6608
Universidade Federal do Estado do Rio de Janeiro · BRUniversidade do Estado do Rio de Janeiro · BRUniversidade Federal do Rio de Janeiro · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Elevated frequency of Th17-like cells expressing Toll-like receptors (TLRs) has been recently associated with relapsing-remitting multiple sclerosis (MS) pathogenesis, a chronic inflammatory demyelinating autoimmune disease of the central nervous system. We aimed to investigate the impact of current major depressive disorder (MDD) on the behaviour of these cells following in vitro stimulation with TLR2, TLR4, TLR5 and TLR9 agonists. Here, the level of both cell proliferation and cytokine production related to Th17/Tc17 phenotypes in response to TLR2 (Pam3C) and TLR4 (LPS) ligands was significantly higher in CD4

Indexed as

AdultAntidepressive Agents, Second-GenerationCase-Control StudiesCD8-Positive T-LymphocytesCell ProliferationCells, CulturedCytokinesFemaleFluoxetineHumansLymphocyte ActivationMajor Depressive DisorderMaleMiddle AgedMultiple Sclerosis, Relapsing-RemittingPhenotypeAntidepressive Agents, Second-GenerationCytokinesFluoxetineSelective Serotonin Reuptake InhibitorsTLR2 protein, humanTLR4 protein, humanToll-Like Receptor 2Toll-Like Receptor 4cytokinesmajor depressive disorderMultiple sclerosisPAMPselective serotonin reuptake inhibitorsserotoninTc17Th17TLR

Identifiers

PMID33112414
PMCPMC7884649
OpenAlexW3094911142

What OpenQuestion holds

Textmetadata
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.