Evidence map›Paper›PMID 23903844›Full record

ArticleJournal of virology2013

Preferential HIV infection of CCR6+ Th17 cells is associated with higher levels of virus receptor expression and lack of CCR5 ligands.

Yelina Alvarez, Michael Tuen, Guomiao Shen, Fatima Nawaz, James Arthos, Martin J Wolff, Michael A Poles, Catarina E Hioe

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed, 1 pooled it
5.0field-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

84 citing papers in PubMed, 1 synthesis or guideline pooled it, 112 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Persistent, Asymptomatic Colonization withMicrobiology spectrum · 2022
    Trial
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Article
  9. HIV Transmission and Immunology of the Male Reproductive Tract.American journal of reproductive immunology (New York, N.Y. : 1989) · 2026
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Characterization ofJournal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  19. Review
  20. Article

24 more citing papers are in PubMed but not listed here.

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 3 institutions in 1 country.

Yelina AlvarezVA Research Service, Department of Veterans Affairs New York Harbor Healthcare System, Manhattan Campus, and Department of Pathology, New York University School of Medicine, New York, New York, USA.
Michael Tuen
Guomiao Shen
Fatima Nawaz
James Arthos
Martin J Wolff
Michael A Poles
Catarina E Hioe
New York University · USVA NY Harbor Healthcare System · USNational Institutes of Health · US

Funding

Vaccines to Induce Functional Antibodies Targeting the V2 Loop P01AI100151 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI KONG, XIANGPENG · 2012 to 2017
$15.4M
Interaction of HIV envelope with cell surface receptorsZIAAI000883 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI ARTHOS, JAMES L · 2009 to 2024
$14.0M
CC Chemokine Secretion to Protect Antigen-Specific CD4 T Cells from HIVR01AI084807 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI HIOE, CATARINA E · 2009 to 2010
$845k
Evaluating self-protection of Th17 cells against HIV-1 by CCR5 Ligands SynthesisF31AI085958 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ALVAREZ, YELINA · 2010 to 2013
$161k
BLRD VA IK6 BX004607NIAID NIH HHS F31 AI085958NIAID NIH HHS P01 AI100151NIAID NIH HHS R01 AI-084807NIAID NIH HHS R01 AI084807
6 · The paper itself

Abstract

Th17 cells are enriched in the gut mucosa and play a critical role in maintenance of the mucosal barrier and host defense against extracellular bacteria and fungal infections. During chronic human immunodeficiency virus (HIV) infection, Th17 cells were more depleted compared to Th1 cells, even when the patients had low or undetectable viremia. To investigate the differential effects of HIV infection on Th17 and Th1 cells, a culture system was used in which CCR6(+) CD4(+) T cells were sorted from healthy human peripheral blood and activated in the presence of interleukin 1β (IL-1β) and IL-23 to drive expansion of Th17 cells while maintaining Th1 cells. HIV infection of these cultures had minimal effects on Th1 cells but caused depletion of Th17 cells. Th17 loss correlated with greater levels of virus-infected cells and cell death. In identifying cellular factors contributing to higher susceptibility of Th17 cells to HIV, we compared Th17-enriched CCR6(+) and Th17-depleted CCR6(-) CD4 T cell cultures and noted that Th17-enriched CCR6(+) cells expressed higher levels of α4β7 and bound HIV envelope in an α4β7-dependent manner. The cells also had greater expression of CD4 and CXCR4, but not CCR5, than CCR6(-) cells. Moreover, unlike Th1 cells, Th17 cells produced little CCR5 ligand, and transfection with one of the CCR5 ligands, MIP-1β (CCL4), increased their resistance against HIV. These results indicate that features unique to Th17 cells, including higher expression of HIV receptors and lack of autocrine CCR5 ligands, are associated with enhanced permissiveness of these cells to HIV.

Indexed as

ApoptosisCD4-Positive T-LymphocytesCells, CulturedChemokine CCL3Chemokine CCL4Chemokine CCL5CytokinesHIV-1HIV InfectionsHumansInterleukin-17Receptors, CCR5Receptors, CCR6Receptors, CXCR4Receptors, VirusTh17 CellsCCL3 protein, humanCCL5 protein, humanCCR5 protein, humanCCR6 protein, humanChemokine CCL3Chemokine CCL4Chemokine CCL5CytokinesInterleukin-17Receptors, CCR5Receptors, CCR6Receptors, CXCR4Receptors, Virus

Identifiers

PMID23903844
PMCPMC3807416
OpenAlexW2158348886

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.