Evidence map›Paper›PMID 17465678›Full record

ArticlePLoS pathogens2007

Identification of a CCR5-expressing T cell subset that is resistant to R5-tropic HIV infection.

Kyra Oswald-Richter, Stacy M Grill, Mindy Leelawong, Michelle Tseng, Spyros A Kalams, Todd Hulgan, David W Haas, Derya Unutmaz

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

47 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
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  6. Article
  7. Review
  8. Dual CCR5/CCR2 targeting: opportunities for the cure of complex disorders.Cellular and molecular life sciences : CMLS · 2019
    Review
  9. Constitutive Siglec-1 expression confers susceptibility to HIV-1 infection of human dendritic cell precursors.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  10. Chemokine receptor CCR5 correlates with functional CD8FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  11. Cytomegalovirus (CMV) Epitope-Specific CD4Journal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  12. Article
  13. Gene Expression Profiles of HIV/AIDS Patients with Qi-Yin Deficiency and Dampness-Heat Retention.Journal of alternative and complementary medicine (New York, N.Y.) · 2016
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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

8 authors at 1 institution in 1 country.

Kyra Oswald-RichterDepartment of Microbiology and Immunology, Vanderbilt University Medical School, Nashville, Tennessee, United States of America.
Stacy M Grill
Mindy Leelawong
Michelle Tseng
Spyros A Kalams
Todd Hulgan
David W Haas
Derya Unutmaz
Vanderbilt University · US

Funding

TCR GENE USAGE AND QUANTITATION OF HIV SPECIFIC CTLR01AI039966 · NIAID · VANDERBILT UNIVERSITY · PI KALAMS, SPYROS A · 1997 to 2006
$3.2M
T Cell Activation Signals That Regulate HIV-1 InfectionR01AI049131 · NIAID · VANDERBILT UNIVERSITY · PI UNUTMAZ, DERYA · 2001 to 2005
$1.6M
NIAID NIH HHS R01 AI039966NIAID NIH HHS R01 AI049131NIAID NIH HHS R01-AI39966NIAID NIH HHS R01-AI49131
6 · The paper itself

Abstract

Infection with HIV-1 perturbs homeostasis of human T cell subsets, leading to accelerated immunologic deterioration. While studying changes in CD4(+) memory and naïve T cells during HIV-1 infection, we found that a subset of CD4(+) effector memory T cells that are CCR7(-)CD45RO(-)CD45RA(+) (referred to as TEMRA cells), was significantly increased in some HIV-infected individuals. This T cell subset displayed a differentiated phenotype and skewed Th1-type cytokine production. Despite expressing high levels of CCR5, TEMRA cells were strikingly resistant to infection with CCR5 (R5)-tropic HIV-1, but remained highly susceptible to CXCR4 (X4)-tropic HIV-1. The resistance of TEMRA cells to R5-tropic viruses was determined to be post-entry of the virus and prior to early viral reverse transcription, suggesting a block at the uncoating stage. Remarkably, in a subset of the HIV-infected individuals, the relatively high proportion of TEMRA cells within effector T cells strongly correlated with higher CD4(+) T cell numbers. These data provide compelling evidence for selection of an HIV-1-resistant CD4(+) T cell population during the course of HIV-1 infection. Determining the host factors within TEMRA cells that restrict R5-tropic viruses and endow HIV-1-specific CD4(+) T cells with this ability may result in novel therapeutic strategies against HIV-1 infection.

Indexed as

AIDS VaccinesApoptosisCD3 ComplexCD4 AntigensCD4 Lymphocyte CountCD4-Positive T-LymphocytesCell DivisionHIV-1HIV InfectionsHumansImmunologic MemoryImmunophenotypingLeukocyte Common AntigensReceptors, CCR5Receptors, CCR7Receptors, ChemokineAIDS VaccinesCCR7 protein, humanCD3 ComplexCD4 AntigensLeukocyte Common AntigensReceptors, CCR5Receptors, CCR7Receptors, Chemokine

Identifiers

PMID17465678
PMCPMC1857714
OpenAlexW2007703708

What OpenQuestion holds

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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.