Evidence map›Paper›PMID 23555011›Full record

ArticlePloS one2013

Combined TLR2/4-activated dendritic/tumor cell fusions induce augmented cytotoxic T lymphocytes.

Shigeo Koido, Sadamu Homma, Masato Okamoto, Yoshihisa Namiki, Kazuki Takakura, Akitaka Takahara, Shunichi Odahara, Shintaro Tsukinaga, Toyokazu Yukawa, Jimi Mitobe and 13 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Biomedicines · 2020
    Review
  5. Article
  6. Immunotherapy for Gastric Cancer: Time for a Personalized Approach?International journal of molecular sciences · 2018
    Review
  7. Dendritic-Tumor Fusion Cell-Based Cancer Vaccines.International journal of molecular sciences · 2016
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
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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

23 authors at 3 institutions in 2 countries.

Shigeo KoidoDivision of Gastroenterology and Hepatology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan. shigeo_koido@jikei.ac.jp
Sadamu Homma
Masato Okamoto
Yoshihisa Namiki
Kazuki Takakura
Akitaka Takahara
Shunichi Odahara
Shintaro Tsukinaga
Toyokazu Yukawa
Jimi Mitobe
Hiroshi Matsudaira
Keisuke Nagatsuma
Kan Uchiyama
Mikio Kajihara
Seiji Arihiro
Hiroo Imazu
Hiroshi Arakawa
Shin Kan
Hideo Komita
Masaki Ito
Toshifumi Ohkusa
Jianlin Gong
Hisao Tajiri
Jikei University School of Medicine · JPBoston University · USKeio University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Induction of antitumor immunity by dendritic cell (DC)-tumor fusion cells (DC/tumor) can be modulated by their activation status. In this study, to address optimal status of DC/tumor to induce efficient antigen-specific cytotoxic T lymphocytes (CTLs), we have created various types of DC/tumor: 1) un-activated DC/tumor; 2) penicillin-killed Streptococcus pyogenes (OK-432; TLR4 agonist)-activated DC/tumor; 3) protein-bound polysaccharides isolated from Coriolus versicolor (PSK; TLR2 agonist)-activated DC/tumor; and 4) Combined OK-432- and PSK-activated DC/tumor. Moreover, we assessed the effects of TGF-β1 derived from DC/tumor on the induction of MUC1-specific CTLs. Combined TLR2- and TLR4-activated DC/tumor overcame immune-suppressive effect of TGF-β1 in comparison to those single activated or un-activated DC/tumor as demonstrated by: 1) up-regulation of MHC class II and CD86 expression on DC/tumor; 2) increased fusion efficiency; 3) increased production of fusions derived IL-12p70; 4) activation of CD4(+) and CD8(+) T cells that produce high levels of IFN-γ; 5) augmented induction of CTL activity specific for MUC1; and 6) superior efficacy in inhibiting CD4(+)CD25(+)Foxp3(+) T cell generation. However, DC/tumor-derived TGF-β1 reduced the efficacy of DC/tumor vaccine in vitro. Incorporating combined TLRs-activation and TGF-β1-blockade of DC/tumor may enhance the effectiveness of DC/tumor-based cancer vaccines and have the potential applicability to the field of adoptive immunotherapy.

Indexed as

B7-2 AntigenCancer VaccinesCell FusionCell Line, TumorDendritic CellsForkhead Transcription FactorsGene Expression RegulationHumansInterferon-gammaInterleukin-12Lymphocyte ActivationMucin-1PicibanilProteoglycansSignal TransductionT-Lymphocytes, CytotoxicB7-2 AntigenCancer VaccinesCD86 protein, humanForkhead Transcription FactorsFOXP3 protein, humanInterferon-gammaInterleukin-12MUC1 protein, humanMucin-1Picibanilpolysaccharide-KProteoglycansTLR2 protein, humanTLR4 protein, humanToll-Like Receptor 2Toll-Like Receptor 4Transforming Growth Factor beta1

Identifiers

PMID23555011
PMCPMC3598755
OpenAlexW1999334634

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.