Evidence map›Paper›PMID 26473478›Full record

ArticlePLoS pathogens2015

Peripheral Vγ9Vδ2 T Cells Are a Novel Reservoir of Latent HIV Infection.

Natalia Soriano-Sarabia, Nancie M Archin, Rosalie Bateson, Noelle P Dahl, Amanda M Crooks, JoAnn D Kuruc, Carolina Garrido, David M Margolis

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 78 citations in OpenAlex.

  1. Trial
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  11. γδ T cells: origin and fate, subsets, diseases and immunotherapy.Signal transduction and targeted therapy · 2023
    Review
  12. Review
  13. Review
  14. HIV Latency in Myeloid Cells: Challenges for a Cure.Pathogens (Basel, Switzerland) · 2022
    Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. 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

8 authors at 1 institution in 1 country.

Natalia Soriano-SarabiaDepartment of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
Nancie M ArchinDepartment of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
Rosalie BatesonDepartment of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
Noelle P DahlDepartment of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
Amanda M CrooksDepartment of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
JoAnn D KurucDepartment of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
Carolina GarridoDepartment of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
David M MargolisDepartment of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America; Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
University of North Carolina at Chapel Hill · US

Funding

Virology, Immunology, and Microbiology CoreP30AI050410 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVID M. MARGOLIS · 2001 to 2026
$76.9M
Using NK Cells to eliminate the latent HIV reservoirU19AI096113 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LUCIW, PAUL · 2011 to 2015
$39.5M
NCRR NIH HHS RR024383NIAID NIH HHS AI50410NIAID NIH HHS P30 AI050410NIAID NIH HHS U19 AI096113
6 · The paper itself

Abstract

Eradication of HIV infection will require the identification of all cellular reservoirs that harbor latent infection. Despite low or lack of CD4 receptor expression on Vδ2 T cells, infection of these cells has previously been reported. We found that upregulation of the CD4 receptor may render primary Vδ2 cells target for HIV infection in vitro and we propose that HIV-induced immune activation may allow infection of γδ T cells in vivo. We assessed the presence of latent HIV infection by measurements of DNA and outgrowth assays within Vδ2 cells in 18 aviremic patients on long-standing antiretroviral therapy. In 14 patients we recovered latent but replication-competent HIV from highly purified Vδ2 cells demonstrating that peripheral Vδ2 T cells are a previously unrecognized reservoir in which latent HIV infection is unexpectedly frequent.

Indexed as

CD4-Positive T-LymphocytesCell SeparationFlow CytometryHIV-1HIV InfectionsHumansReceptors, Antigen, T-Cell, gamma-deltaT-Lymphocyte SubsetsVirus LatencyReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID26473478
PMCPMC4608739
OpenAlexW2232375730

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.