Evidence map›Paper›PMID 19679552›Full record

ArticleCancer research2009

IFN-producing killer dendritic cells are antigen-presenting cells endowed with T-cell cross-priming capacity.

Maria Pletneva, Hongni Fan, Jang-June Park, Vedran Radojcic, Chunfa Jie, Yanxing Yu, Camie Chan, Alec Redwood, Drew Pardoll, Franck Housseau

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02661685 (An Immunotherapy for Metastatic Cancer Patients by Adoptive Transfer of Autologous IKDC-like Cells - Phase 1 Clinical Trial), which is not on this map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-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.

NCT02661685 phase1completednot on this mapstarted 2016, after this paper: background citation

An Immunotherapy for Metastatic Cancer Patients by Adoptive Transfer of Autologous IKDC-like Cells - Phase 1 Clinical Trial

TypeinterventionalSponsorNational Defense Medical Center, TaiwanRan2016 to 2019Enrolled6ConditionsNeoplasm MetastasisArmsautologous IKDC-like cells
3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. A role for pre-mNK cells in tumor progression.Journal for immunotherapy of cancer · 2016
    Article
  3. Depletion of B220Oncoimmunology · 2015
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
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

10 authors at 4 institutions in 2 countries.

Maria PletnevaSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, Maryland 21231, USA.
Hongni Fan
Jang-June Park
Vedran Radojcic
Chunfa Jie
Yanxing Yu
Camie Chan
Alec Redwood
Drew Pardoll
Franck Housseau
Sidney Kimmel Comprehensive Cancer Center · USJohns Hopkins Medicine · USUniversity of California, Davis · USUniversity of Western Australia · AU

Funding

PANCREAS CANCER MESOTHELIN ANIMAL MODELU19CA113341 · NCI · JOHNS HOPKINS UNIVERSITY · PI WU, TZYY-CHOOU · 2005 to 2009
$5.7M
Identification of Novel Immune Cell- the NKDCR01AI064826 · NIAID · JOHNS HOPKINS UNIVERSITY · PI PARDOLL, DREW M. · 2006 to 2010
$2.0M
NCI NIH HHS 5U19CA113 341NIAID NIH HHS R01 AI064826
6 · The paper itself

Abstract

IFN-producing killer dendritic cells (IKDC) represent a recently discovered cell type in the immune system that possesses a number of functions contributing to innate and adaptive immunity, including production of type 1 and 2 IFNs, interleukin (IL)-12, natural killing, and ultimately antigen presentation to naïve T cells. Here, we compared in vitro and in vivo responses of mouse IKDC, conventional dendritic cells (DC), and natural killer (NK) cells to murine cytomegalovirus infection and found distinct functions among these cell subsets. Upon recognition of infected fibroblasts, IKDC, as well as NK, produced high level of IFN-gamma, but unlike NK, IKDC simultaneously produced IL-12p40 and up-regulated MHC class II (MHC-II) and costimulatory molecules. Using MHC-II molecule expression as a phenotypic marker to distinguish activated IKDC from activated NK, we further showed that highly purified MHC-II(+) IKDC but not NK cross-present MHC class I-restricted antigens derived from MCMV-infected targets to CD8(+) T cells in vitro and in vivo. Our findings emphasize the unique nature of IKDC as a killer antigen-presenting cell directly linking innate and adaptive immunity.

Indexed as

AnimalsAntigen-Presenting CellsCells, CulturedCross-PrimingCytotoxicity, ImmunologicDendritic CellsInterferonsInterleukin-12MiceMice, Inbred BALB CMice, Inbred C57BLMice, KnockoutMice, SCIDMyeloid Differentiation Factor 88T-LymphocytesInterferonsInterleukin-12Myd88 protein, mouseMyeloid Differentiation Factor 88

Identifiers

PMID19679552
PMCPMC2761009
OpenAlexW2034689050

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.