Evidence map›Paper›PMID 20430958›Full record

ArticleBlood2010

Virally infected and matured human dendritic cells activate natural killer cells via cooperative activity of plasma membrane-bound TNF and IL-15.

Lazar Vujanovic, David E Szymkowski, Sean Alber, Simon C Watkins, Nikola L Vujanovic, Lisa H Butterfield

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

43 citing papers in PubMed, 66 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Review
  5. Review
  6. Article
  7. TNFα and Immune Checkpoint Inhibition: Friend or Foe for Lung Cancer?International journal of molecular sciences · 2021
    Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Infection and immunity · 2019
    Article
  15. Article
  16. CD56Frontiers in immunology · 2019
    Article
  17. Article
  18. Review
  19. Article
  20. Lessons learned from cancer vaccine trials and target antigen choice.Cancer immunology, immunotherapy : CII · 2016
    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 1 country.

Lazar VujanovicDepartment of Pathology and Immunology, University of Pittsburgh, Hillman Cancer Center, 5117 Centre Ave., Pittsburgh, PA 15213, USA.
David E Szymkowski
Sean Alber
Simon C Watkins
Nikola L Vujanovic
Lisa H Butterfield
UPMC Hillman Cancer Center · USXencor (United States) · US

Funding

Therapuetic Immune Targeting of EphA2 Expressed by Melanoma & Its Tumor-AssociateP50CA121973 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KIRKWOOD, JOHN MUNN · 2008 to 2018
$22.9M
NK cell-dendritic cell interaction cancerR01DE017150 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VUJANOVIC, NIKOLA LAZAR · 2007 to 2011
$1.8M
AFP-BASED PRIME-BOOST IMMUNOTHERAPY OF HCCR01CA104524 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BUTTERFIELD, LISA HELENE · 2004 to 2006
$898k
NCI NIH HHS 1P50CA121973NCI NIH HHS P50 CA121973NCI NIH HHS R01 CA104524NCI NIH HHS R01CA104524NIDCR NIH HHS R01 DE017150NIDCR NIH HHS R01 DE17150
6 · The paper itself

Abstract

Recombinant adenovirus-engineered dendritic cells (Ad.DCs) are potent immunologic adjuvants of antiviral and anticancer vaccines. The effectiveness of Ad.DC-based vaccines may depend on the ability of Ad.DCs to crosstalk with natural killer (NK) cells and to activate, polarize, and bridge innate and adaptive immunity. We investigated, for the first time, whether and how human Ad.DCs activate NK cells, and compared the Ad.DC function with that of immature DCs and matured DCs (mDCs). We found that adenovirus transduction and lipopolysaccharide/interferon-gamma-induced maturation increased expression of transmembrane tumor necrosis factor (TNF) and trans-presented (trans) interleukin-15 (IL-15) on DCs, leading to enhanced NK cell activation without enhancing DC susceptibility to NK cell-mediated killing. This crosstalk enhanced NK cell CD69 expression, interferon-gamma secretion, proliferation, and antitumor activities, with Ad.DCs being significantly more effective than immature DCs, but less effective than mDCs. The Ad.DC and mDC crosstalk with NK cells was largely prevented by physical separation of DCs and NK cells, and neutralization of total TNF and IL-15, but not by selective sequestration of soluble TNF. These findings demonstrate that both Ad.DCs and mDCs can efficiently promote innate immune functions by activation of NK cells through the cooperative activities of tmTNF and trans-IL-15 mediated by cell-to-cell contact.

Indexed as

Cell CommunicationAdenoviridae InfectionsAnimalsCell DifferentiationCell MembraneCells, CulturedDendritic CellsFemaleHumansImmunity, InnateInterleukin-15K562 CellsKiller Cells, NaturalLymphocyte ActivationMiceMice, Inbred NODInterleukin-15Tumor Necrosis Factor-alpha

Identifiers

PMID20430958
PMCPMC3324291
OpenAlexW2029578639

What OpenQuestion holds

Textmetadata
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.