Evidence map›Paper›PMID 11927631›Full record

ArticleThe Journal of experimental medicine2002

CD1d-restricted human natural killer T cells are highly susceptible to human immunodeficiency virus 1 infection.

Alison Motsinger, David W Haas, Aleksandar K Stanic, Luc Van Kaer, Sebastian Joyce, Derya Unutmaz

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

100 citing papers in PubMed, 214 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. CD3Journal of neuroimmunology · 2023
    Article
  9. Article
  10. Review
  11. Article
  12. Preferential and persistent impact of acute HIV-1 infection on CD4Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  13. Review
  14. Review
  15. Invariant Natural Killer T-cell Dynamics in Human Immunodeficiency Virus-associated Tuberculosis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2020
    Article
  16. Article
  17. Dendritic Cell Maturation Regulates TSPAN7 Function in HIV-1 Transfer to CD4Frontiers in cellular and infection microbiology · 2020
    Article
  18. Suppression of R5-type of HIV-1 in CD4Scientific reports · 2019
    Article
  19. Article
  20. Liver as a target of human immunodeficiency virus infection.World journal of gastroenterology · 2018
    Review

40 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

6 authors at 2 institutions in 1 country.

Alison MotsingerDepartment of Microbiology and Immunology, Vanderbilt University Medical School, Nashville, TN 37232, USA.
David W Haas
Aleksandar K Stanic
Luc Van Kaer
Sebastian Joyce
Derya Unutmaz
Vanderbilt University · USHoward Hughes Medical Institute · US

Funding

MOLECULAR BASIS OF CDLDL AND NATURAL T CELL FUNCTIONR01AI042284 · NIAID · VANDERBILT UNIVERSITY · PI JOYCE, SEBASTIAN · 1998 to 2013
$3.1M
T Cell Activation Signals That Regulate HIV-1 InfectionR01AI049131 · NIAID · VANDERBILT UNIVERSITY · PI UNUTMAZ, DERYA · 2001 to 2005
$1.6M
NIAID NIH HHS R01 AI042284NIAID NIH HHS R01 AI049131NIAID NIH HHS R01-AI42284NIAID NIH HHS R01-AI49131
6 · The paper itself

Abstract

Human natural killer (NK) T cells are unique T lymphocytes that express an invariant T cell receptor (TCR) Valpha24-Vbeta11 and have been implicated to play a role in various diseases. A subset of NKT cells express CD4 and hence are potential targets for human immunodeficiency virus (HIV)-1 infection. We demonstrate that both resting and activated human Valpha24(+) T cells express high levels of the HIV-1 coreceptors CCR5 and Bonzo (CXCR6), but low levels of CCR7, as compared with conventional T cells. Remarkably NKT cells activated with alpha-galactosylceramide (alpha-GalCer)-pulsed dendritic cells were profoundly more susceptible to infection with R5-tropic, but not X4-tropic, strains of HIV-1, compared with conventional CD4(+) T cells. Furthermore, resting CD4(+) NKT cells were also more susceptible to infection. After initial infection, HIV-1 rapidly replicated and depleted the CD4(+) subset of NKT cells. In addition, peripheral blood NKT cells were markedly and selectively depleted in HIV-1 infected individuals. Although the mechanisms of this decline are not clear, low numbers or absence of NKT cells may affect the course of HIV-1 infection. Taken together, our findings indicate that CD4(+) NKT cells are directly targeted by HIV-1 and may have a potential role during viral transmission and spread in vivo.

Indexed as

Acquired Immunodeficiency SyndromeAdultAntigens, CDAntigens, CD1Antigens, CD1dCell Culture TechniquesDendritic CellsDisease SusceptibilityHIV-1HIV InfectionsHIV SeronegativityHumansImmunophenotypingKiller Cells, NaturalLipopolysaccharide ReceptorsReceptors, Antigen, T-Cell, alpha-betaAntigens, CDAntigens, CD1Antigens, CD1dCCR7 protein, humanCD1D protein, humanLipopolysaccharide ReceptorsReceptors, Antigen, T-Cell, alpha-betaReceptors, CCR7Receptors, ChemokineReceptors, CXCR4

Identifiers

PMID11927631
PMCPMC2193731
OpenAlexW2123832762

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.