Evidence map›Paper›PMID 19863675›Full record

ArticleJournal of medical primatology2009

CD4 T cell subsets in the mucosa are CD28+Ki-67-HLA-DR-CD69+ but show differential infection based on alpha4beta7 receptor expression during acute SIV infection.

M Kader, S Bixler, M Roederer, R Veazey, J J Mattapallil

Open access · greenAbstract read
In one paragraph

Article in Journal of medical primatology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

29 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  6. Review
  7. Preferential Infection of α4β7+ Memory CD4+ T Cells During Early Acute Human Immunodeficiency Virus Type 1 Infection.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2020
    Article
  8. Article
  9. Article
  10. Article
  11. Intestinal CD4 Depletion in HIV / SIV Infection.Current immunology reviews · 2019
    Article
  12. Article
  13. Integrin αJournal of immunology (Baltimore, Md. : 1950) · 2018
    Article
  14. Article
  15. Article
  16. Article
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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

5 authors at 2 institutions in 1 country.

M KaderUniformed Services University of Health Sciences, Bethesda, MD 20814, USA.
S Bixler
M Roederer
R Veazey
J J Mattapallil
Uniformed Services University of the Health Sciences · USTulane University · US

Funding

T Cell Dynamics In SIV-infected MacaquesZIAAI005019 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI ROEDERER, MARIO · 2009 to 2014
$3.5M
Mucosal Epithelium and Long-Term Anti-Retroviral TherapyR21DE018339 · NIDCR · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI MATTAPALLIL, JOSEPH JOHN · 2007 to 2008
$673k
CD4 T cells and anti-viral control in SIV infectionK22AI071812 · NIAID · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI MATTAPALLIL, JOSEPH JOHN · 2007 to 2008
$270k
NIAID NIH HHS K22 AI071812NIAID NIH HHS K22AI07812NIDCR NIH HHS R21 DE018339NIDCR NIH HHS R21DE018339
6 · The paper itself

Abstract

backgroundCD4 T cell depletion in the mucosa has been well documented during acute HIV and SIV infections. The demonstration the HIV/SIVcan use the alpha4beta7 receptor for viral entry suggests that these viruses selectively target CD4 T cells in the mucosa that express high levels of alpha4beta7 receptor.

methodsMucosal samples obtained from SIV infected rhesus macaques during the early phase of infection were used for immunophenotypic analysis. CD4 T cell subsets were sorted based on the expression of beta7 and CD95 to quantify the level of SIV infection in different subsets of CD4 T cells. Changes in IL-17, IL-21, IL-23 and TGFbeta mRNA expression was determined using Taqman PCR.

resultsCD4 T cells in the mucosa were found to harbor two major population of cells; -25% of CD4 T cells expressed the alpha4(+)beta7(hi) phenotype, whereas the rest of the 75% expressed an alpha4(+)beta7(int) phenotype. Both the subsets were predominantly CD28(+)Ki-67(-)HLA-DR(-) but CD69(+), and expressed detectable levels of CCR5 on their surface. Interestingly, however, alpha4(+)beta7(hi)CD4 T cells were found to harbor more SIV than the alpha4(+)beta7(int) subsets at day 10 pi. Early infection was associated with a dramatic increase in the expression of IL-17, and IL-17 promoting cytokines IL-21, IL-23, and TGFbeta that stayed high even after the loss of mucosal CD4 T cells.

conclusionsOur results suggest that the differential expression of the alpha4beta7 receptor contributes to the differences in the extent of infection in CD4 T cell subsets in the mucosa. Early infection is associated dysregulation of the IL-17 network in mucosal tissues involves other non-Th-17 cells that likely contributes to the pro-inflammatory environment in the mucosa during acute stages of SIV infection.

Indexed as

Immunity, MucosalAnimalsAntigens, CDAntigens, Differentiation, T-LymphocyteCD28 AntigensCD4-Positive T-LymphocytesCD69 AntigensInterleukin-17Lectins, C-TypeMacaca mulattaReceptors, Antigen, T-Cell, alpha-betaSimian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusTransforming Growth Factor betaAntigens, CDAntigens, Differentiation, T-LymphocyteCD28 AntigensCD69 AntigensInterleukin-17Lectins, C-TypeReceptors, Antigen, T-Cell, alpha-betaTransforming Growth Factor beta

Identifiers

PMID19863675
PMCPMC2813512
OpenAlexW2002915050

What OpenQuestion holds

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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.