Evidence map›Paper›PMID 26372382›Full record

ArticleAIDS (London, England)2015

Lysis of HIV-1-infected autologous CD4+ primary T cells by interferon-alpha-activated NK cells requires NKp46 and NKG2D.

Costin Tomescu, Domenico Mavilio, Luis J Montaner

Open access · greenAbstract read
In one paragraph

Article in AIDS (London, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

35 citing papers in PubMed, 44 citations in OpenAlex.

  1. Trial
  2. Review
  3. CXCR6Frontiers in immunology · 2026
    Article
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  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. IL-18 Responsiveness Defines Limitations in Immune Help for Specialized FcRγJournal of immunology (Baltimore, Md. : 1950) · 2020
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Impact of Myeloid Reservoirs in HIV Cure Trials.Current HIV/AIDS reports · 2019
    Review
  17. Article
  18. Article
  19. 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

3 authors at 2 institutions in 2 countries.

Costin TomescuaHIV Immunopathogenesis Laboratory, The Wistar Institute, Philadelphia, Pennsylvania, USA bUnit of Clinical and Experimental Immunology, Humanitas Clinical and Research Center, Rozzano cDepartment of Medical Biotechnologies and Translational Medicine, University of Milan, Milan, Italy.
Domenico Mavilio
Luis J Montaner
The Wistar Institute · USUniversity of Milan · IT

Funding

Virus & Reservoirs CoreP30AI045008 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ROBERT GROSS · 1999 to 2026
$78.6M
Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
TRAINING IN HIV PATHOGENESIST32AI007632 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI Frederic D Bushman, James L. Riley · 2000 to 2026
$10.6M
Antiviral activity of Peg-IFN alpha in chronic HIV-1U01AI065279 · NIAID · WISTAR INSTITUTE · PI MONTANER, LUIS J · 2005 to 2009
$2.8M
APCs and Innate Immunity in HIV DiseaseR01AI051225 · NIAID · WISTAR INSTITUTE · PI MONTANER, LUIS J. · 2002 to 2005
$1.6M
ANTI-HIV-1 EFFECTS OF IL-13 ON MACROPHAGES AND T CELLSR01AI047760 · NIAID · WISTAR INSTITUTE · PI MONTANER, LUIS J. · 2000 to 2004
$1.5M
Direct/Indirect NK Activation by HIV-1 Infected CellsF32AI068405 · NIAID · WISTAR INSTITUTE · PI TOMESCU, COSTIN · 2006 to 2007
$62k
NCI NIH HHS P30 CA010815NCI NIH HHS P30CA010815NIAID NIH HHS AI068405NIAID NIH HHS AI07632NIAID NIH HHS AI47760NIAID NIH HHS AI51225NIAID NIH HHS F32 AI068405NIAID NIH HHS P30 AI045008NIAID NIH HHS R01 AI047760NIAID NIH HHS R01 AI051225NIAID NIH HHS T32 AI007632NIAID NIH HHS U01 AI065279NIAID NIH HHS U01AI065279
6 · The paper itself

Abstract

objectiveAutologous HIV-1-infected CD4 primary T cells (aHIVCD4) have been shown to be largely resistant to natural killer (NK)-cell-mediated lysis because of viral strategies of immune evasion. We have previously shown that a preactivation of NK cells with plasmacytoid dendritic cells can significantly augment lysis of aHIVCD4 through a mechanism dependent on interferon-alpha (IFN-α).

designThe goal of the present study is to identify the specific NK-activating receptors involved in NK lysis of aHIVCD4 following IFN-α activation.

methodsPeripheral blood mononuclear cells (PBMC) were incubated with aHIVCD4 to induce the secretion of endogenous levels of IFN-α and drive NK activation. We then utilized a standard chromium lysis assay to assess the degree of IFN-α-activated lysis of aHIVCD4 in the presence or absence of masking antibodies to a panel of NK-activating receptors and co-receptors.

resultsDirect recognition of HIV-1-infected, but not uninfected, autologous CD4 primary T cells by PBMC induced the secretion IFN-α (median 2280 pg/ml, P < 0.001, n = 9) that, in turn, activated NK cells (P < 0.001, n = 12) and significantly increased their cytolytic potential against aHIVCD4 (P < 0.01, n = 12). The masking of NKp46 (P < 0.01, n = 8) and NKG2D (P < 0.05, n = 8), but not 2B4, NTBA, NKp30 or NKp44, significantly reduced IFN-α-activated lysis of aHIVCD4.

conclusionsTaken together, these results demonstrate that endogenous levels of IFN-α secreted by plasmacytoid dendritic cells induce NK cells to lyse aHIVCD4 via the engagement of NKp46 and NKG2D.

Indexed as

Cytotoxicity, ImmunologicCD4-Positive T-LymphocytesCells, CulturedCytotoxicity Tests, ImmunologicHIV-1HIV InfectionsHumansInterferon-alphaKiller Cells, NaturalNatural Cytotoxicity Triggering Receptor 1NK Cell Lectin-Like Receptor Subfamily KInterferon-alphaKLRK1 protein, humanNatural Cytotoxicity Triggering Receptor 1NCR1 protein, humanNK Cell Lectin-Like Receptor Subfamily K

Identifiers

PMID26372382
PMCPMC4571461
OpenAlexW2404017401

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.