Evidence map›Paper›PMID 18566447›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

Fusions of dendritic cells with breast carcinoma stimulate the expansion of regulatory T cells while concomitant exposure to IL-12, CpG oligodeoxynucleotides, and anti-CD3/CD28 promotes the expansion of activated tumor reactive cells.

Baldev Vasir, Zekui Wu, Keith Crawford, Jacalyn Rosenblatt, Corrine Zarwan, Adam Bissonnette, Donald Kufe, David Avigan

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.4field-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

20 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Immunotherapy for Breast Cancer Treatment.Iranian biomedical journal · 2021
    Article
  5. Review
  6. Dendritic-Tumor Fusion Cell-Based Cancer Vaccines.International journal of molecular sciences · 2016
    Review
  7. Article
  8. Article
  9. Review
  10. Lenalidomide enhances anti-myeloma cellular immunity.Cancer immunology, immunotherapy : CII · 2013
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Regulation of tumor immunity by tumor/dendritic cell fusions.Clinical & developmental immunology · 2010
    Review
  18. Article
  19. Review
  20. 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

8 authors at 3 institutions in 1 country.

Baldev VasirDana-Farber Cancer Institute, Dana-Farber/Harvard Cancer Center, Brigham & Women's Hospital, Boston, MA 02115, USA.
Zekui Wu
Keith Crawford
Jacalyn Rosenblatt
Corrine Zarwan
Adam Bissonnette
Donald Kufe
David Avigan
Dana-Farber Cancer Institute · USBeth Israel Deaconess Medical Center · USBrigham and Women's Hospital · US

Funding

Novel Serum, Plasma, and Urine Biomarkers of Ovarian CanP50CA105009 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI CRAMER, DANIEL WILLIAM · 2004 to 2010
$13.3M
NCI NIH HHS P50 CA105009NCI NIH HHS P50CA105009-04
6 · The paper itself

Abstract

Vaccination of patients with dendritic cell (DC)/breast carcinoma fusions stimulated antitumor immune responses in a majority of patients with metastatic disease but only a subset demonstrate evidence of tumor regression. To define the factors that limit vaccine efficacy, we examined the biological characteristics of DC/breast carcinoma fusions as APCs and the nature of the vaccine-mediated T cell response. We demonstrate that fusion of DCs with breast carcinoma cells up-regulates expression of costimulatory and maturation markers and results in high levels of expression of IL-12 consistent with their role as activated APCs. Fusion cells also express the chemokine receptor CCR7, consistent with their ability to migrate to the draining lymph node. However, DC/breast cancer fusions stimulate a mixed T cell response characterized by the expansion of both activated and regulatory T cell populations, the latter of which is characterized by expression of CTLA-4, FOXP3, IL-10, and the suppression of T cell responses. Our results demonstrate that IL-12, IL-18, and TLR 9 agonist CpG oligodeoxynucleotides reduce the level of fusion-mediated regulatory T cell expansion. Our results also demonstrate that sequential stimulation with DC/breast carcinoma fusions and anti-CD3/CD28 results in the marked expansion of activated tumor-specific T cells. These findings suggest that DC/breast carcinoma fusions are effective APCs, but stimulate inhibitory T cells that limit vaccine efficacy. In contrast, exposure to TLR agonists, stimulatory cytokines, and anti-CD3/CD28 enhances vaccine efficacy by limiting the regulatory T cell response and promoting expansion of activated effector cells.

Indexed as

AntibodiesBreast NeoplasmsCD28 AntigensCD3 ComplexCell DifferentiationCell FusionCell ProliferationCells, CulturedDendritic CellsHumansInterleukin-10Interleukin-12Lymphocyte ActivationMucin-1OligonucleotidesPhenotypeAntibodiesCCR7 protein, humanCD28 AntigensCD3 ComplexInterleukin-10Interleukin-12MUC1 protein, humanMucin-1OligonucleotidesReceptors, CCR7

Identifiers

PMID18566447
PMCPMC2938172
OpenAlexW1697880118

What OpenQuestion holds

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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.