Evidence map›Paper›PMID 26108174›Full record

ArticleNature communications2015

IL-21 induces antiviral microRNA-29 in CD4 T cells to limit HIV-1 infection.

Stanley Adoro, Juan R Cubillos-Ruiz, Xi Chen, Maud Deruaz, Vladimir D Vrbanac, Minkyung Song, Suna Park, Thomas T Murooka, Timothy E Dudek, Andrew D Luster and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

44 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
  2. Article
  3. The STAT Signaling Pathway in HIV-1 Infection: Roles and Dysregulation.International journal of molecular sciences · 2025
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Cytokines and microRNAs in SARS-CoV-2: What do we know?Molecular therapy. Nucleic acids · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Selective miRNA inhibition in CD8Frontiers in immunology · 2022
    Article
  16. Article
  17. IL-36β promotes anti-tumor effects in CD8Annals of translational medicine · 2021
    Article
  18. Article
  19. Deficiency ofAging · 2021
    Article
  20. Interleukin-21 in Viral Infections.International journal of molecular sciences · 2021
    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 5 institutions in 2 countries.

Stanley AdoroDepartment of Medicine, Weill Cornell Medical College, Cornell University, 1300 York Avenue, New York, New York 10065, USA.
Juan R Cubillos-RuizDepartment of Medicine, Weill Cornell Medical College, Cornell University, 1300 York Avenue, New York, New York 10065, USA.
Xi ChenDepartment of Medicine, Weill Cornell Medical College, Cornell University, 1300 York Avenue, New York, New York 10065, USA.
Maud DeruazCenter for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Charlestown, Massachusetts 02129, USA.
Vladimir D VrbanacRagon Institute of MGH, MIT and Harvard, Cambridge, Massachusetts 02139, USA.
Minkyung SongDepartment of Medicine, Weill Cornell Medical College, Cornell University, 1300 York Avenue, New York, New York 10065, USA.
Suna ParkDepartment of Medicine, Weill Cornell Medical College, Cornell University, 1300 York Avenue, New York, New York 10065, USA.
Thomas T MurookaCenter for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Charlestown, Massachusetts 02129, USA.
Timothy E DudekRagon Institute of MGH, MIT and Harvard, Cambridge, Massachusetts 02139, USA.
Andrew D LusterCenter for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Charlestown, Massachusetts 02129, USA.
Andrew M TagerRagon Institute of MGH, MIT and Harvard, Cambridge, Massachusetts 02139, USA.
Hendrik StreeckInstitute for Medical Biology, University Hospital Essen, University of Duisburg-Essen, Essen D-45147, Germany.
Brittany BowmanRagon Institute of MGH, MIT and Harvard, Cambridge, Massachusetts 02139, USA.
Bruce D WalkerRagon Institute of MGH, MIT and Harvard, Cambridge, Massachusetts 02139, USA.
Douglas S KwonRagon Institute of MGH, MIT and Harvard, Cambridge, Massachusetts 02139, USA.
Vanja LazarevicExperimental Immunology Branch, National Cancer Institute, NIH, Bethesda, Maryland 20892, USA.
Laurie H GlimcherDepartment of Medicine, Weill Cornell Medical College, Cornell University, 1300 York Avenue, New York, New York 10065, USA.
Ragon Institute of MGH, MIT and Harvard · USCornell University · USMassachusetts General Hospital · USNational Cancer Institute · USUniversity of Duisburg-Essen · DE

Funding

The impact of HIV viral diversity and cellular immunity on HIV pathogenesisP30AI060354 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI ROBERT A. PARKER · 2004 to 2026
$94.4M
Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1991 to 2026
$35.3M
P3: Chemokine-Mediated T Cell Trafficking in HIV Transmission and Immune ResponseP01AI112521 · NIAID · HARVARD MEDICAL SCHOOL · PI LUSTER, ANDREW · 2014 to 2018
$9.8M
Generation and Function of NK Cell MemoryR01AI111595 · NIAID · HARVARD MEDICAL SCHOOL · PI VON ANDRIAN, ULRICH H · 2013 to 2017
$4.1M
T-bet and the Th1/Th17 balance in Acute HIV infectionR21AI087475 · NIAID · HARVARD SCHOOL OF PUBLIC HEALTH · PI GLIMCHER, LAURIE HOLLIS · 2010 to 2011
$442k
NIAID NIH HHS 1R21AI087475-01NIAID NIH HHS P01 AI112521NIAID NIH HHS P30 AI060354NIAID NIH HHS P30AI060354NIAID NIH HHS R01 AI111595NIAID NIH HHS R21 AI087475NIDDK NIH HHS P30 DK043351
6 · The paper itself

Abstract

Initial events after exposure determine HIV-1 disease progression, underscoring a critical need to understand host mechanisms that interfere with initial viral replication. Although associated with chronic HIV-1 control, it is not known whether interleukin-21 (IL-21) contributes to early HIV-1 immunity. Here we take advantage of tractable primary human lymphoid organ aggregate cultures to show that IL-21 directly suppresses HIV-1 replication, and identify microRNA-29 (miR-29) as an antiviral factor induced by IL-21 in CD4 T cells. IL-21 promotes transcription of all miR-29 species through STAT3, whose binding to putative regulatory regions within the MIR29 gene is enriched by IL-21 signalling. Notably, exogenous IL-21 limits early HIV-1 infection in humanized mice, and lower viremia in vivo is associated with higher miR-29 expression. Together, these findings reveal a novel antiviral IL-21-miR-29 axis that promotes CD4 T-cell-intrinsic resistance to HIV-1 infection, and suggest a role for IL-21 in initial HIV-1 control in vivo.

Indexed as

AnimalsAntibodies, Monoclonal, HumanizedCD4-Positive T-LymphocytesHIV-1HIV InfectionsHumansInterleukin-21InterleukinsMiceMice, KnockoutMicroRNAsSpleenTissue Culture TechniquesAntibodies, Monoclonal, HumanizedInterleukin-21InterleukinsMicroRNAsMIRN29a microRNA, human

Identifiers

PMID26108174
PMCPMC4481879
OpenAlexW1005468862

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.