Evidence map›Paper›PMID 35585332›Full record

ArticleCellular and molecular life sciences : CMLS2022

Major depression favors the expansion of Th17-like cells and decrease the proportion of CD39

Priscila Mendonça do Sacramento, Marisa Sales, Taissa de Matos Kasahara, Clarice Monteiro, Hugo Oyamada, Aleida Soraia Oliveira Dias, Lana Lopes, Camilla Teixeira Castro, Átila Duque Rossi, Lucas Mattos Milioni and 4 more

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. The emerging role of T cells in depression.Frontiers in psychiatry · 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

14 authors at 4 institutions in 2 countries.

Priscila Mendonça do SacramentoDepartment of Microbiology and Parasitology, Federal University of the State of Rio de Janeiro, Frei Caneca 94, Rio de Janeiro, RJ, 20261-040, Brazil. pri.men.sac@gmail.com.ORCID http://orcid.org/0000-0003-0788-3195
Marisa SalesDepartment of Microbiology and Parasitology, Federal University of the State of Rio de Janeiro, Frei Caneca 94, Rio de Janeiro, RJ, 20261-040, Brazil.
Taissa de Matos KasaharaDepartment of Microbiology and Parasitology, Federal University of the State of Rio de Janeiro, Frei Caneca 94, Rio de Janeiro, RJ, 20261-040, Brazil.
Clarice MonteiroDepartment of Immunology, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Hugo OyamadaDepartment of Microbiology and Parasitology, Federal University of the State of Rio de Janeiro, Frei Caneca 94, Rio de Janeiro, RJ, 20261-040, Brazil.
Aleida Soraia Oliveira DiasDepartment of Microbiology and Parasitology, Federal University of the State of Rio de Janeiro, Frei Caneca 94, Rio de Janeiro, RJ, 20261-040, Brazil.
Lana LopesDepartment of Microbiology and Parasitology, Federal University of the State of Rio de Janeiro, Frei Caneca 94, Rio de Janeiro, RJ, 20261-040, Brazil.
Camilla Teixeira CastroDepartment of Microbiology and Parasitology, Federal University of the State of Rio de Janeiro, Frei Caneca 94, Rio de Janeiro, RJ, 20261-040, Brazil.
Átila Duque RossiDepartment of Genetics, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Lucas Mattos MilioniDepartment of Genetics, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Anshu AgrawalUniversity of California, Irvine, CA, USA.
Regina AlvarengaDepartment of General Medicine, Federal University of the State of Rio de Janeiro, Rio de Janeiro, Brazil.
Claudia Cristina VasconcelosDepartment of General Medicine, Federal University of the State of Rio de Janeiro, Rio de Janeiro, Brazil.
Cleonice Alves de Melo BentoDepartment of Microbiology and Parasitology, Federal University of the State of Rio de Janeiro, Frei Caneca 94, Rio de Janeiro, RJ, 20261-040, Brazil. cbento@unirio.br.
Universidade do Estado do Rio de Janeiro · BRUniversidade Federal do Rio de Janeiro · BRUniversidade Federal do Estado do Rio de Janeiro · BRUniversity of California, Irvine · US

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 301.780/2017-0Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/202.940/2017
6 · The paper itself

Abstract

backgroundMood disorders have been associated with risk of clinical relapses in multiple sclerosis (MS), a demyelinating disease mediated by myelin-specific T cells.

objectivesWe aimed to investigate the impact of major depressive disorder (MDD) and cytokine profile of T-cells in relapsing remitting MS patients.

methodsFor our study, plasma and PBMC were obtained from 60 MS patients (30 with lifetime MDD) in remission phase. The PBMC cultures were stimulated with anti-CD3/anti-CD28 beads or myelin basic protein (MBP), and effector and regulatory T cell phenotypes were determined by flow cytometry. The cytokine levels, both in the plasma or in the supernatants collected from PBMC cultures, were quantified by Luminex. In some experiments, the effect of serotonin (5-HT) was investigated.

resultsHere, higher Th17-related cytokine levels in response to anti-CD3/anti-CD28 and MBP were quantified in the plasma and PBMC cultures of the MS/MDD group in comparison with MS patients. Further, elevated frequency of CD4

conclusionsIn summary, our findings suggested that recurrent major depression, by favoring imbalances of effector Th17 and Treg cell subsets, contributes to MS severity.

Indexed as

ApyraseAutoantigensMajor Depressive DisorderMultiple SclerosisMyelin SheathTh17 CellsT-Lymphocytes, RegulatoryCD8-Positive T-LymphocytesCytokinesGranulocyte-Macrophage Colony-Stimulating FactorHumansInterleukin-17Leukocytes, MononuclearSerotoninApyraseAutoantigensCytokinesENTPD1 protein, humanGranulocyte-Macrophage Colony-Stimulating FactorInterleukin-17SerotoninCD39Major depressive disorderMultiple sclerosisSerotoninTh17 cellsTreg

Identifiers

PMID35585332
PMCPMC11073410
OpenAlexW4280544090

What OpenQuestion holds

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Registered trials

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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.