Evidence map›Paper›PMID 18670213›Full record

ArticleAIDS (London, England)2008

IL-21 augments natural killer effector functions in chronically HIV-infected individuals.

Natasa Strbo, Lesley de Armas, Huanliang Liu, Michael A Kolber, Mathias Lichtenheld, Savita Pahwa

Open access · greenAbstract read
In one paragraph

Article in AIDS (London, England), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

28 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
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  9. Induction ofJournal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  10. Article
  11. Review
  12. IL-21 Signaling in Immunity.F1000Research · 2016
    Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Loss and dysregulation of Th17 cells during HIV infection.Clinical & developmental immunology · 2013
    Review
  20. 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

6 authors at 2 institutions in 2 countries.

Natasa StrboCenter for HIV Research, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.
Lesley de Armas
Huanliang Liu
Michael A Kolber
Mathias Lichtenheld
Savita Pahwa
Bipar · FRUniversity of Miami · US

Funding

University of Miami Developmental Center for AIDS Research (D-CFAR)P30AI073961 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI ALLAN E RODRIGUEZ · 2007 to 2026
$33.8M
Role of IL21 in HIV InfectionR01AI077501 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI PAHWA, SAVITA · 2008 to 2011
$1.5M
IL-21 effects on CD8 Memory T Cells in HIV InfectionR03AI065293 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI PAHWA, SAVITA · 2005 to 2006
$150k
NIAID NIH HHS AI065293NIAID NIH HHS P30 AI073961NIAID NIH HHS R01 AI077501NIAID NIH HHS R03 AI065293
6 · The paper itself

Abstract

objectiveThis study addresses the interleukin (IL)-21 effects on resting peripheral blood natural killer (NK) cells in chronically HIV-infected individuals.

designThe effects of IL-21 on perforin expression, proliferation, degranulation, interferon (IFN)-gamma production, cytotoxicity and induction of STAT phosphorylation in NK cells were determined in vitro.

methodsPeripheral blood mononuclear cells from HIV-infected and healthy individuals were incubated in vitro for 6 h, 24 h or 5 days with IL-21 or IL-15. Percentages of perforin, IFN-gamma, CD107a, NKG2D and STAT3-5 positive cells were determined within NK cell populations. K562 cells were used as target cells in NK cytotoxicity assay.

resultsFrequency of CD56 cells in chronically HIV-infected individuals was diminished. Perforin expression in CD56 and CD56 was comparable in healthy and HIV-infected individuals. IL-15 upregulated perforin expression primarily in CD56 NK cells, whereas IL-21 upregulated perforin in both NK subsets. IL-21 and IL-15 upregulated CD107a and IFN-gamma, as well as NK cytotoxicity. IL-15 predominantly activated STAT5, whereas IL-21 activated STAT5 and STAT3. IL-15, but not IL-21 increased NK cell proliferation in uninfected and HIV-infected individuals.

conclusionIL-21 augments NK effector functions in chronically HIV-infected individuals and due to its perforin enhancing properties it has potential for immunotherapy or as a vaccine adjuvant.

Indexed as

AdultBiomarkersCase-Control StudiesCD56 AntigenCell ProliferationCells, CulturedChronic DiseaseCytotoxicity Tests, ImmunologicHIV InfectionsHumansInterferon-gammaInterleukin-15Interleukin-21InterleukinsKiller Cells, NaturalLysosomal-Associated Membrane Protein 1BiomarkersCD56 AntigenInterferon-gammaInterleukin-15Interleukin-21InterleukinsLysosomal-Associated Membrane Protein 1PerforinSTAT3 Transcription FactorSTAT5 Transcription Factor

Identifiers

PMID18670213
PMCPMC2665999
OpenAlexW2008531095

What OpenQuestion holds

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LicenceTDM
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.