Evidence map›Paper›PMID 15389286›Full record

ArticleCancer gene therapy2005

Immunological properties and vaccine efficacy of murine dendritic cells simultaneously expressing melanoma-associated antigen and interleukin-12.

Naoki Okada, Sayaka Iiyama, Yuka Okada, Hiroyuki Mizuguchi, Takao Hayakawa, Shinsaku Nakagawa, Tadanori Mayumi, Takuya Fujita, Akira Yamamoto

Abstract read
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In one paragraph

Article in Cancer gene therapy, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. New insights into IL-12-mediated tumor suppression.Cell death and differentiation · 2015
    Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Optimizing DC vaccination by combination with oncolytic adenovirus coexpressing IL-12 and GM-CSF.Molecular therapy : the journal of the American Society of Gene Therapy · 2011
    Article
  10. Article
  11. Engineering dendritic cells to enhance cancer immunotherapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2011
    Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Dendritic cells in immunotherapy of established cancer: Roles of signals 1, 2, 3 and 4.Current opinion in investigational drugs (London, England : 2000) · 2009
    Review
  17. Article
  18. Immunotherapy of cancer by IL-12-based cytokine combinations.Expert opinion on biological therapy · 2007
    Review
  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

9 authors at 3 institutions in 1 country.

Naoki OkadaDepartment of Biopharmaceutics, Kyoto Pharmaceutical University, 5 Nakauchi-cho, Misasagi, Yamashina-ku, Kyoto 607-8414, Japan. okada@mb.kyoto-phu.ac.jp
Sayaka Iiyama
Yuka Okada
Hiroyuki Mizuguchi
Takao Hayakawa
Shinsaku Nakagawa
Tadanori Mayumi
Takuya Fujita
Akira Yamamoto
Kyoto Pharmaceutical University · JPOsaka University · JPNational Institute of Health Sciences · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin (IL)-12 is a key factor for inducing cellular immune responses, which play a central role in the eradication of cancer. In the present study, in order to create a dendritic cell (DC)-based vaccine capable of positively skewing immune response toward a cellular immunity-dominant state, we analyzed immunological characteristics and vaccine efficacy of DCs cotransduced with melanoma-associated antigen (gp100) and IL-12 gene (gp100+IL12/DCs) by using RGD fiber-mutant adenovirus vector (AdRGD), which enables highly efficient gene transduction into DCs. gp100+IL12/DCs could simultaneously express cytoplasmic gp100 and secretory IL-12 at levels comparable to DCs transduced with each gene alone. In comparison with DCs transduced with gp100 alone (gp100/DCs), upregulation of major histocompatibility complex class I, CD40, and CD86 molecules on the cell surface and more potent T-cell-stimulating ability for proliferation and interferon-gamma secretion were observed as characteristic changes in gp100+IL12/DCs. In addition, administration of gp100+IL12/DCs, which were prepared by a relatively low dose of AdRGD-IL12, could induce more potent tumor-specific cellular immunity in the murine B16BL6 melanoma model than vaccination with gp100/DCs. However, antitumor effect and B16BL6-specific cytotoxic T-lymphocyte activity in mice vaccinated with gp100+IL12/DCs diminished with increasing AdRGD-IL12 dose during gene transduction, and paralleled the decrease in presentation levels via MHC class I molecules for antigen transduced with another AdRGD. Collectively, our results suggested that optimization of combined vector dose was required for development of a more efficacious DC-based vaccine for cancer immunotherapy, which relied on genetic engineering to simultaneously express tumor-associated antigen and IL-12.

Indexed as

Cancer VaccinesAdenoviridaeAnimalsAntigens, NeoplasmAntigens, SurfaceDendritic CellsFemaleGenetic EngineeringInterleukin-12MelanomaMelanoma-Specific AntigensMiceMice, Inbred C57BLNeoplasm ProteinsT-Lymphocytes, CytotoxicTransduction, GeneticAntigens, NeoplasmAntigens, SurfaceCancer VaccinesInterleukin-12Melanoma-Specific AntigensNeoplasm Proteins

Identifiers

PMID15389286
OpenAlexW2090730094

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.