Evidence map›Paper›PMID 19380802›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

An anti-vascular endothelial growth factor receptor 2/fetal liver kinase-1 Listeria monocytogenes anti-angiogenesis cancer vaccine for the treatment of primary and metastatic Her-2/neu+ breast tumors in a mouse model.

Matthew M Seavey, Paulo C Maciag, Nada Al-Rawi, Duane Sewell, Yvonne Paterson

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
6.4field-weighted citation impact, top 4% 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

44 citing papers in PubMed, 69 citations in OpenAlex.

  1. B cells in cancer: functions, mechanisms and therapeutic advances.Signal transduction and targeted therapy · 2026
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  2. Combined radiation andMolecular therapy. Oncology · 2026
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  13. Article
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  17. White paper on microbial anti-cancer therapy and prevention.Journal for immunotherapy of cancer · 2018
    Review
  18. Vaccines · 2018
    Review
  19. Article
  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

5 authors at 1 institution in 1 country.

Matthew M SeaveyDepartment of Microbiology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
Paulo C Maciag
Nada Al-Rawi
Duane Sewell
Yvonne Paterson
University of Pennsylvania · US

Funding

IMMUNOBIOLOGY OF NORMAL AND NEOPLASTIC LYMPHOCYTEST32CA009140 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Malay Haldar, WARREN S PEAR · 1985 to 2026
$16.1M
Immunotherapeutic strategies for breast cancerR01CA109253 · NCI · UNIVERSITY OF PENNSYLVANIA · PI PATERSON, YVONNE J · 2006 to 2010
$1.2M
NCI NIH HHS 5R01CA109253-03NCI NIH HHS R01 CA109253NCI NIH HHS T32 CA009140NCI NIH HHS T32CA09140
6 · The paper itself

Abstract

Thirty years after angiogenesis was shown to play an enabling role in cancer, modern medicine is still trying to develop novel compounds and therapeutics to target the tumor vasculature. However, most therapeutics require multiple rounds of administration and can have toxic side effects. In this study, we use anti-angiogenesis immunotherapy to target cells actively involved in forming new blood vessels that support the growth and spread of breast cancer. Targeting a central cell type involved in angiogenesis, endothelial cells, we immunized against host vascular endothelial growth factor receptor 2 to fight the growth of Her-2/neu(+) breast tumors. Using the bacterial vector, Listeria monocytogenes (Lm), we fused polypeptides from the mouse vascular endothelial growth factor receptor 2 molecule (fetal liver kinase-1) to the microbial adjuvant, listeriolysin-O, and used Lm to deliver the Ags and elicit potent antitumor CTL responses. Lm-listeriolysin-O-fetal liver kinase-1 was able to eradicate some established breast tumors, reduce microvascular density in the remaining tumors, protect against tumor rechallenge and experimental metastases, and induce epitope spreading to various regions of the tumor-associated Ag Her-2/neu. Tumor eradication was found to be dependent on epitope spreading to HER-2/neu and was not solely due to the reduction of tumor vasculature. However, vaccine efficacy did not affect normal wound healing nor have toxic side effects on pregnancy. We show that an anti-angiogenesis vaccine can overcome tolerance to the host vasculature driving epitope spreading to an endogenous tumor protein and drive active tumor regression.

Indexed as

Amino Acid SequenceAngiogenesis InhibitorsAnimalsBacterial ToxinsCancer VaccinesCell Line, TumorErb-b2 Receptor Tyrosine KinasesFemaleGrowth InhibitorsHeat-Shock ProteinsHemolysin ProteinsListeria monocytogenesLung NeoplasmsMammary Neoplasms, ExperimentalMiceMice, Inbred BALB CAngiogenesis InhibitorsBacterial ToxinsCancer VaccinesErb-b2 Receptor Tyrosine KinasesGrowth InhibitorsHeat-Shock ProteinsHemolysin ProteinshlyA protein, Listeria monocytogenesRecombinant Fusion ProteinsVascular Endothelial Growth Factor Receptor-2

Identifiers

PMID19380802
PMCPMC2850569
OpenAlexW1835770933

What OpenQuestion holds

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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.