Evidence map›Paper›PMID 21384340›Full record

ArticleInternational journal of cancer2011

Parenteral is more efficient than mucosal immunization to induce regression of human papillomavirus-associated genital tumors.

Loane Decrausaz, Sonia Domingos-Pereira, Mélanie Duc, Martine Bobst, Pedro Romero, John T Schiller, Patrice Jichlinski, Denise Nardelli-Haefliger

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in International journal of cancer, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 33 citations in OpenAlex.

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  10. LocalOncoimmunology · 2015
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  11. Review
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  13. Immunotherapeutic strategies for bladder cancer.Human vaccines & immunotherapeutics · 2014
    Article
  14. Article
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  16. Article
  17. Review
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  19. 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 4 institutions in 2 countries.

Loane DecrausazDepartment of Urology, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland.
Sonia Domingos-Pereira
Mélanie Duc
Martine Bobst
Pedro Romero
John T Schiller
Patrice Jichlinski
Denise Nardelli-Haefliger
University Hospital of Lausanne · CHUniversity of Lausanne · CHLudwig Cancer Research · CHNational Cancer Institute · US

Funding

Understanding Papillomavirus Virion Proteins and VaccinesZIABC009052 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SCHILLER, JOHN T. · 2009 to 2025
$38.4M
Papillomavirus Virion Proteins and Vaccines Z01BC009052 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SCHILLER, JOHN T. · 1996 to 2008
$3.3M
Intramural NIH HHS Z01 BC009052
6 · The paper itself

Abstract

Cervical cancer is a public health concern as it represents the second cause of cancer death in women worldwide. High-risk human papillomaviruses (HPV) are the etiologic agents, and HPV E6 and/or E7 oncogene-specific therapeutic vaccines are under development to treat HPV-related lesions in women. Whether the use of mucosal routes of immunization may be preferable for inducing cell-mediated immune responses able to eradicate genital tumors is still debated because of the uniqueness of the female genital mucosa (GM) and the limited experimentation. Here, we compared the protective activity resulting from immunization of mice via intranasal (i.n.), intravaginal (IVAG) or subcutaneous (s.c.) routes with an adjuvanted HPV type 16 E7 polypeptide vaccine. Our data show that s.c. and i.n. immunizations elicited similar frequencies and avidity of TetE71CD81 and E7-specific Interferon-gamma-secreting cells in the GM, whereas slightly lower immune responses were induced by IVAG immunization. In a novel orthotopic murine model, both s.c. and i.n. immunizations allowed for complete long-term protection against genital E7-expressing tumor challenge. However, only s.c. immunization induced complete regression of already established genital tumors. This suggests that the higher E7-specific systemic response observed after s.c. immunization may contribute to the regression of growing genital tumors, whereas local immune responses may be sufficient to impede genital challenges. Thus, our data show that for an efficiently adjuvanted protein-based vaccine, parenteral vaccination route is superior to mucosal vaccination route for inducing regression of established genital tumors in a murine model of HPV-associated genital cancer.

Indexed as

Administration, IntranasalAdministration, IntravaginalAnimalsCancer VaccinesFemaleImmunity, CellularInfusions, ParenteralMiceMice, Inbred C57BLMucous MembranePapillomaviridaePapillomavirus E7 ProteinsPapillomavirus InfectionsPapillomavirus VaccinesUterine Cervical NeoplasmsVaccinationCancer VaccinesPapillomavirus E7 ProteinsPapillomavirus Vaccines

Identifiers

PMID21384340
PMCPMC7462631
OpenAlexW2005146925

What OpenQuestion holds

Textmetadata
LicenceTDM
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.