Evidence map›Paper›PMID 35163318›Full record

ArticleInternational journal of molecular sciences2022

Interplay between Selenium, Selenoproteins and HIV-1 Replication in Human CD4 T-Lymphocytes.

Olivia M Guillin, Caroline Vindry, Théophile Ohlmann, Laurent Chavatte

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 24 citations in OpenAlex.

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  13. Zinc Uptake by HIV-1 Viral Particles: An Isotopic Study.International journal of molecular sciences · 2023
    Article
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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

4 authors at 1 institution in 1 country.

Olivia M GuillinCentre International de Recherche en Infectiologie (CIRI), 69007 Lyon, France.
Caroline VindryCentre International de Recherche en Infectiologie (CIRI), 69007 Lyon, France.
Théophile OhlmannCentre International de Recherche en Infectiologie (CIRI), 69007 Lyon, France.ORCID 0000-0002-2001-8916
Laurent ChavatteCentre International de Recherche en Infectiologie (CIRI), 69007 Lyon, France.ORCID 0000-0001-7696-2431
Université Claude Bernard Lyon 1 · FR

Funding

Agence Nationale de Recherches sur le Sida et les Hépatites Virales ANRSAgence Nationale de Recherches sur le Sida et les Hépatites Virales Post-doctoral fellowship to CVClaude Bernard University Lyon 1 PhD fellowship to OGÉcole Normale Supérieure de Lyon projet emergent 2016École Normale Supérieure de Lyon projet emergent 2018French National Centre for Scientific Research CNRS MITI programs "Isotop"French National Centre for Scientific Research CNRS MITI programs "Metallo-Mix"
6 · The paper itself

Abstract

The infection of CD4 T-lymphocytes with human immunodeficiency virus (HIV), the etiological agent of acquired immunodeficiency syndrome (AIDS), disrupts cellular homeostasis, increases oxidative stress and interferes with micronutrient metabolism. Viral replication simultaneously increases the demand for micronutrients and causes their loss, as for selenium (Se). In HIV-infected patients, selenium deficiency was associated with a lower CD4 T-cell count and a shorter life expectancy. Selenium has an important role in antioxidant defense, redox signaling and redox homeostasis, and most of these biological activities are mediated by its incorporation in an essential family of redox enzymes, namely the selenoproteins. Here, we have investigated how selenium and selenoproteins interplay with HIV infection in different cellular models of human CD4 T lymphocytes derived from established cell lines (Jurkat and SupT1) and isolated primary CD4 T cells. First, we characterized the expression of the selenoproteome in various human T-cell models and found it tightly regulated by the selenium level of the culture media, which was in agreement with reports from non-immune cells. Then, we showed that selenium had no significant effect on HIV-1 protein production nor on infectivity, but slightly reduced the percentage of infected cells in a Jurkat cell line and isolated primary CD4 T cells. Finally, in response to HIV-1 infection, the selenoproteome was slightly altered.

Indexed as

Acquired Immunodeficiency SyndromeAntioxidantsCD4-Positive T-LymphocytesCell Line, TumorGlutathione PeroxidaseHEK293 CellsHIV-1HIV InfectionsHumansJurkat CellsOxidative StressSeleniumSelenoproteinsVirus ReplicationAntioxidantsGlutathione PeroxidaseSeleniumSelenoproteinsglutathione peroxidaseHIV-1Jurkatprimary T cellsSELENOOselenoproteomeSELENOSSupT1thioredoxin reductasetranslational controlviral infection

Identifiers

PMID35163318
PMCPMC8835795
OpenAlexW4210509071

What OpenQuestion holds

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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.