Evidence map›Paper›PMID 17146630›Full record

ArticleCancer immunology, immunotherapy : CII2007

Vaccination with an adenoviral vector expressing calreticulin-human papillomavirus 16 E7 fusion protein eradicates E7 expressing established tumors in mice.

Jorge G Gomez-Gutierrez, Kutlu G Elpek, Roberto Montes de Oca-Luna, Haval Shirwan, H Sam Zhou, Kelly M McMasters

Open access · bronzeAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

38 citing papers in PubMed, 85 citations in OpenAlex.

  1. Review
  2. Review
  3. Current and future direction in treatment of HPV-related cervical disease.Journal of molecular medicine (Berlin, Germany) · 2022
    Review
  4. Prophylactic and Therapeutic HPV Vaccines: Current Scenario and Perspectives.Frontiers in cellular and infection microbiology · 2022
    Review
  5. Review
  6. Review
  7. Article
  8. Cervical Cancer Immunotherapy: Facts and Hopes.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Review
  9. Development of HPVBiotechnology letters · 2020
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. The Journey ofFrontiers in immunology · 2018
    Review
  16. Article
  17. Review
  18. Article
  19. Perspectives for therapeutic HPV vaccine development.Journal of biomedical science · 2016
    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

6 authors at 2 institutions in 3 countries.

Jorge G Gomez-GutierrezDepartment of Surgery, University of Louisville School of Medicine, James Graham Brown Cancer Center, Louisville, KY 40292, USA.
Kutlu G Elpek
Roberto Montes de Oca-Luna
Haval Shirwan
H Sam Zhou
Kelly M McMasters
University of Louisville · USUniversidad Autónoma de Nuevo León · MX

Funding

E2F-1 Cancer Gene TherapyR01CA090784 · NCI · UNIVERSITY OF LOUISVILLE · PI MCMASTERS, KELLY M · 2002 to 2005
$970k
NCI NIH HHS R01 CA090784NCI NIH HHS R01CA90784-01A1
6 · The paper itself

Abstract

backgroundCervical cancer remains a leading cause of cancer-related mortality in women, particularly in developing countries. The causal association between genital human papilloma virus (HPV) infection and cervical cancer has been firmly established, and the oncogenic potential of certain HPV types has been clearly demonstrated. Vaccines targeting the oncogenic proteins, E6 and E7 of HPV-16 and -18 are the focus of current vaccine development. Previous studies have shown that calreticulin (CRT) enhances the MHC class I presentation of linked peptide/protein and may serve as an effective vaccination strategy for antigen-specific cancer treatment.

methodsTwo replication-deficient adenoviruses, one expressing HPV-16 E7 (Ad-E7) and the other expressing CRT linked to E7 (Ad-CRT/E7), were assessed for their ability to induce cellular immune response and tested for prophylactic and therapeutic effects in an E7-expressing mouse tumor model.

resultsVaccination with Ad-CRT/E7 led to a dramatic increase in E7-specific T cell proliferation, interferon (IFN)-gamma-secretion, and cytotoxic activity. Immunization of mice with Ad-CRT/E7 was effective in preventing E7-expressing tumor growth, as well as eradicating established tumors with long-term immunological memory.

conclusionVaccination with an adenoviral vector expressing CRT-E7 fusion protein represents an effective strategy for immunotherapy of cervical cancer in rodents, with possible therapeutic potential in clinical settings.

Indexed as

Papillomavirus VaccinesAdenoviridaeAnimalsCalreticulinCell ProliferationFemaleGenetic VectorsHumansInterferon-gammaMiceMice, Inbred C57BLMicroscopy, ConfocalOncogene Proteins, ViralPapillomavirus E7 ProteinsPapillomavirus InfectionsRecombinant Fusion ProteinsCalreticulinInterferon-gammaoncogene protein E7, Human papillomavirus type 16Oncogene Proteins, ViralPapillomavirus E7 ProteinsPapillomavirus VaccinesRecombinant Fusion Proteins

Identifiers

PMID17146630
PMCPMC11030956
OpenAlexW2091744461

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.