Evidence map›Paper›PMID 22470433›Full record

ArticlePloS one2012

The colocalization potential of HIV-specific CD8+ and CD4+ T-cells is mediated by integrin β7 but not CCR6 and regulated by retinoic acid.

Vanessa Sue Wacleche, Nicolas Chomont, Annie Gosselin, Patricia Monteiro, Mathieu Goupil, Hassen Kared, Cécile Tremblay, Nicole Bernard, Mohamed-Rachid Boulassel, Jean-Pierre Routy and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 38% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. FoxP3Frontiers in immunology · 2022
    Article
  6. CD16Blood advances · 2018
    Article
  7. Characterization ofJournal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Persistent HIV-1 replication is associated with lower antiretroviral drug concentrations in lymphatic tissues.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  14. 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

11 authors at 4 institutions in 2 countries.

Vanessa Sue WaclecheDepartment of Microbiology and Immunology, Université de Montréal, Montreal, Quebec, Canada.
Nicolas Chomont
Annie Gosselin
Patricia Monteiro
Mathieu Goupil
Hassen Kared
Cécile Tremblay
Nicole Bernard
Mohamed-Rachid Boulassel
Jean-Pierre Routy
Petronela Ancuta
Université de Montréal · CACentre Hospitalier de l’Université de Montréal · CAMcGill University Health Centre · CAVaccine & Gene Therapy Institute of Florida · US

Funding

Washington University Institute of Clinical and Translational Sciences (UL1)UL1RR024992 · NCRR · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2007 to 2011
$45.4M
The influence of genotype on the outcome of gene transfer in beta-thalassemiaR01HL102449 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI RIVELLA, STEFANO · 2010 to 2014
$2.1M
Gene therapy for Cooley's anemia in a new mouse modelK01DK063992 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI RIVELLA, STEFANO · 2004 to 2010
$667k
CIHR HBF-82849CIHR HOP-103230CIHR MOP-82849CIHR MOP-93770NCRR NIH HHS UL1 RR024992NHLBI NIH HHS R01 HL102449NIDDK NIH HHS K01 DK063992
6 · The paper itself

Abstract

CD4(+) T-cells from gut-associated lymphoid tissues (GALT) are major targets for HIV-1 infection. Recruitment of excess effector CD8(+) T-cells in the proximity of target cells is critical for the control of viral replication. Here, we investigated the colocalization potential of HIV-specific CD8(+) and CD4(+) T-cells into the GALT and explored the role of retinoic acid (RA) in regulating this process in a cohort of HIV-infected subjects with slow disease progression. The expression of the gut-homing molecules integrin β7, CCR6, and CXCR3 was identified as a "signature" for HIV-specific but not CMV-specific CD4(+) T-cells thus providing a new explanation for their enhanced permissiveness to infection in vivo. HIV-specific CD8(+) T-cells also expressed high levels of integrin β7 and CXCR3; however CCR6 was detected at superior levels on HIV-specific CD4(+) versus CD8(+) T-cells. All trans RA (ATRA) upregulated the expression of integrin β7 but not CCR6 on HIV-specific T-cells. Together, these results suggest that HIV-specific CD8(+) T-cells may colocalize in excess with CD4(+) T-cells into the GALT via integrin β7 and CXCR3, but not via CCR6. Considering our previous findings that CCR6(+)CD4(+) T-cells are major cellular targets for HIV-DNA integration in vivo, a limited ability of CD8(+) T-cells to migrate in the vicinity of CCR6(+)CD4(+) T-cells may facilitate HIV replication and dissemination at mucosal sites.

Indexed as

CD4-Positive T-LymphocytesCD8-Positive T-LymphocytesHIVHIV InfectionsHumansIntegrin beta ChainsKeratolytic AgentsReceptors, CCR4Receptors, CCR6Receptors, CXCR3TretinoinUp-RegulationCCR4 protein, humanCCR6 protein, humanCXCR3 protein, humanintegrin beta7Integrin beta ChainsKeratolytic AgentsReceptors, CCR4Receptors, CCR6Receptors, CXCR3Tretinoin

Identifiers

PMID22470433
PMCPMC3314661
OpenAlexW2028362556

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.