Evidence map›Paper›PMID 34612140›Full record

ArticleAutophagy2022

Autophagy-dependent glutaminolysis drives superior IL21 production in HIV-1-specific CD4 T cells.

Hamza Loucif, Xavier Dagenais-Lussier, Daina Avizonis, Luc Choinière, Cherifa Beji, Léna Cassin, Jean-Pierre Routy, Jörg H Fritz, David Olagnier, Julien van Grevenynghe

Open access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

11 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Glutaminolysis of CD4Journal of inflammation research · 2024
    Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
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

10 authors at 4 institutions in 2 countries.

Hamza LoucifInstitut National de la Recherche Scientifique (INRS)-Centre Armand-Frappier Santé Biotechnologie, Laval, Quebec, Canada.ORCID 0000-0002-2646-524X
Xavier Dagenais-LussierInstitut National de la Recherche Scientifique (INRS)-Centre Armand-Frappier Santé Biotechnologie, Laval, Quebec, Canada.
Daina AvizonisMetabolomics Innovation Resource, Rosalind and Morris Goodman Cancer Center, McGill University, Montreal, QC, Canada.
Luc ChoinièreMetabolomics Innovation Resource, Rosalind and Morris Goodman Cancer Center, McGill University, Montreal, QC, Canada.
Cherifa BejiInstitut National de la Recherche Scientifique (INRS)-Centre Armand-Frappier Santé Biotechnologie, Laval, Quebec, Canada.
Léna CassinDepartment of Biomedicine, Research Center for Innate Immunology, Aarhus University, Aarhus, Denmark.
Jean-Pierre RoutyChronic Viral Illness Service and Division of Hematology, McGill University Health Centre, Montreal, Quebec, Canada.
Jörg H FritzDepartment of Microbiology and Immunology, McGill University, Montreal, Quebec, Canada.
David OlagnierDepartment of Biomedicine, Research Center for Innate Immunology, Aarhus University, Aarhus, Denmark.
Julien van GrevenyngheInstitut National de la Recherche Scientifique (INRS)-Centre Armand-Frappier Santé Biotechnologie, Laval, Quebec, Canada.
Institut National de la Recherche Scientifique · CAMcGill University · CAAarhus University · DKMcGill University Health Centre · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The maintenance of a strong IL21 production in memory CD4 T cells, especially in HIV-1-specific cells, represents a major correlate of natural immune protection against the virus. However, the molecular mechanisms underlying IL21 production during HIV-1 infection, which is only elevated among the naturally protected elite controllers (EC), are still unknown. We recently found out that lipophagy is a critical immune mediator that control an antiviral metabolic state following CD8A T cell receptor engagement, playing an important role in the natural control of HIV-1 infection. This led us to investigate whether the beneficial role of a strong macroautophagy/autophagy, could also be used to ensure effective IL21 production as well. Herein, we confirm that after both polyclonal and HIV-1-specific activation, memory CD4 T cells (Mem) from EC display enhanced activity of the autophagy-mediated proteolysis compared to ART. Our results indicate that the enhanced autophagy activity in EC was controlled by the energy-sensing PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1). We further confirmed the critical role of the autophagy-mediated proteolysis in the strong IL21 production in EC by using

Indexed as

AutophagyHIV-1Adenosine MonophosphateAntiviral AgentsCD4-Positive T-LymphocytesHumansInterleukin-21InterleukinsLeukocytes, MononuclearProtein KinasesAdenosine MonophosphateAntiviral AgentsInterleukin-21InterleukinsProtein KinasesAntiretroviral therapyautophagy-mediated proteolysiselite controllersglutaminolysisHIV-1IL21PRKAA1

Identifiers

PMID34612140
PMCPMC9225533
OpenAlexW3203222542

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.