Evidence map›Paper›PMID 31042779›Full record

ArticlePLoS pathogens2019

FOXO1 transcription factor plays a key role in T cell-HIV-1 interaction.

Arthur Roux, Héloise Leroy, Bénédicte De Muylder, Lucie Bracq, Samia Oussous, Isabelle Dusanter-Fourt, Ghina Chougui, Rachida Tacine, Clotilde Randriamampita, Delphine Desjardins and 7 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. FOXO1 or not FOXO1: that is the question.Cancer communications (London, England) · 2025
    Article
  8. Review
  9. Role ofSaudi journal of biological sciences · 2023
    Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Targeting HIV-1 proviral transcription.Current opinion in virology · 2019
    Review
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

17 authors at 2 institutions in 2 countries.

Arthur RouxNSERM, U1016, Institut Cochin, Paris, France.
Héloise LeroyNSERM, U1016, Institut Cochin, Paris, France.
Bénédicte De MuylderNSERM, U1016, Institut Cochin, Paris, France.
Lucie BracqNSERM, U1016, Institut Cochin, Paris, France.
Samia OussousNSERM, U1016, Institut Cochin, Paris, France.ORCID 0000-0001-7741-2976
Isabelle Dusanter-FourtNSERM, U1016, Institut Cochin, Paris, France.ORCID 0000-0002-9286-1021
Ghina ChouguiNSERM, U1016, Institut Cochin, Paris, France.
Rachida TacineNSERM, U1016, Institut Cochin, Paris, France.ORCID 0000-0003-4505-7484
Clotilde RandriamampitaNSERM, U1016, Institut Cochin, Paris, France.ORCID 0000-0001-8594-7831
Delphine DesjardinsCEA, Université Paris Sud, INSERM -Immunology of Viral Infections and Autoimmune Diseases department (IMVA), U1184, IDMIT Department, Fontenay-aux-Roses, France.ORCID 0000-0002-5820-3914
Roger Le GrandCEA, Université Paris Sud, INSERM -Immunology of Viral Infections and Autoimmune Diseases department (IMVA), U1184, IDMIT Department, Fontenay-aux-Roses, France.ORCID 0000-0002-4928-4484
Frederic BouillaudNSERM, U1016, Institut Cochin, Paris, France.
Serge BenichouNSERM, U1016, Institut Cochin, Paris, France.
Florence Margottin-GoguetNSERM, U1016, Institut Cochin, Paris, France.ORCID 0000-0002-3124-6690
Remi CheynierNSERM, U1016, Institut Cochin, Paris, France.
Georges BismuthNSERM, U1016, Institut Cochin, Paris, France.
Marianne MangeneyNSERM, U1016, Institut Cochin, Paris, France.ORCID 0000-0002-9102-191X
Délégation Paris 5 · FRUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HIV-1 is dependent on the host cell for providing the metabolic resources for completion of its viral replication cycle. Thus, HIV-1 replicates efficiently only in activated CD4+ T cells. Barriers preventing HIV-1 replication in resting CD4+ T cells include a block that limits reverse transcription and also the lack of activity of several inducible transcription factors, such as NF-κB and NFAT. Because FOXO1 is a master regulator of T cell functions, we studied the effect of its inhibition on T cell/HIV-1 interactions. By using AS1842856, a FOXO1 pharmacologic inhibitor, we observe that FOXO1 inhibition induces a metabolic activation of T cells with a G0/G1 transition in the absence of any stimulatory signal. One parallel outcome of this change is the inhibition of the activity of the HIV restriction factor SAMHD1 and the activation of the NFAT pathway. FOXO1 inhibition by AS1842856 makes resting T cells permissive to HIV-1 infection. In addition, we found that FOXO1 inhibition by either AS1842856 treatment or upon FOXO1 knockdown induces the reactivation of HIV-1 latent proviruses in T cells. We conclude that FOXO1 has a central role in the HIV-1/T cell interaction and that inhibiting FOXO1 with drugs such as AS1842856 may be a new therapeutic shock-and-kill strategy to eliminate the HIV-1 reservoir in human T cells.

Indexed as

Gene Expression RegulationVirus ReplicationAnimalsCD4-Positive T-LymphocytesCell CycleForkhead Box Protein O1HIV-1HIV InfectionsHumansJurkat CellsLymphocyte ActivationMacaca fascicularisMaleVirus ActivationVirus LatencyForkhead Box Protein O1FOXO1 protein, human

Identifiers

PMID31042779
PMCPMC6513100
OpenAlexW2942745234

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.