Evidence map›Paper›PMID 25763880›Full record

ArticleJournal of translational medicine2015

A prime/boost strategy using DNA/fowlpox recombinants expressing the genetically attenuated E6 protein as a putative vaccine against HPV-16-associated cancers.

Massimiliano Bissa, Elena Illiano, Sole Pacchioni, Francesca Paolini, Carlo Zanotto, Carlo De Giuli Morghen, Silvia Massa, Rosella Franconi, Antonia Radaelli, Aldo Venuti

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.8field-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

14 citing papers in PubMed, 27 citations in OpenAlex.

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  3. Advances in nucleic acid-based cancer vaccines.Journal of biomedical science · 2025
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  14. Clinical significance of human papillomavirus genotyping.Journal of gynecologic oncology · 2016
    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

10 authors at 2 institutions in 1 country.

Massimiliano BissaDepartment of Pharmacological and Biomolecular Sciences, Università di Milano, Milan, Italy. massimiliano.bissa@unimi.it.
Elena IllianoDepartment of Pharmacological and Biomolecular Sciences, Università di Milano, Milan, Italy. elena.illiano@unimi.it.
Sole PacchioniDepartment of Medical Biotechnologies and Translational Medicine, Università di Milano, Milan, Italy. sole.pacchioni@studenti.unimi.it.
Francesca PaoliniLaboratory of Virology HPV-UNIT, Regina Elena National Cancer Institute, Rome, Italy. paolini@ifo.it.
Carlo ZanottoDepartment of Medical Biotechnologies and Translational Medicine, Università di Milano, Milan, Italy. carlo.zanotto@unimi.it.
Carlo De Giuli MorghenDepartment of Medical Biotechnologies and Translational Medicine, Università di Milano, Milan, Italy. carlo.degiulimorghen@unimi.it.
Silvia MassaTechnical Unit of Radiation Biology and Human Health, Italian National Agency for New Technologies, Energy and Sustainable Economic Development (ENEA), Casaccia Research Centre, Rome, Italy. silvia.massa@enea.it.
Rosella FranconiTechnical Unit of Radiation Biology and Human Health, Italian National Agency for New Technologies, Energy and Sustainable Economic Development (ENEA), Casaccia Research Centre, Rome, Italy. rosella.franconi@enea.it.
Antonia RadaelliDepartment of Pharmacological and Biomolecular Sciences, Università di Milano, Milan, Italy. antonia.radaelli@unimi.it.
Aldo VenutiLaboratory of Virology HPV-UNIT, Regina Elena National Cancer Institute, Rome, Italy. venuti@ifo.it.
University of Milan · ITNational Agency for New Technologies, Energy and Sustainable Economic Development · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundConsidering the high number of new cases of cervical cancer each year that are caused by human papilloma viruses (HPVs), the development of an effective vaccine for prevention and therapy of HPV-associated cancers, and in particular against the high-risk HPV-16 genotype, remains a priority. Vaccines expressing the E6 and E7 proteins that are detectable in all HPV-positive pre-cancerous and cancer cells might support the treatment of HPV-related lesions and clear already established tumors.

methodsIn this study, DNA and fowlpox virus recombinants expressing the E6F47R mutant of the HPV-16 E6 oncoprotein were generated, and their correct expression verified by RT-PCR, Western blotting and immunofluorescence. Immunization protocols were tested in a preventive or therapeutic pre-clinical mouse model of HPV-16 tumorigenicity using heterologous (DNA/FP) or homologous (DNA/DNA and FP/FP) prime/boost regimens. The immune responses and therapeutic efficacy were evaluated by ELISA, ELISPOT assays, and challenge with TC-1* cells.

resultsIn the preventive protocol, while an anti-E6-specific humoral response was just detectable, a specific CD8(+) cytotoxic T-cell response was elicited in immunized mice. After the challenge, there was a delay in cancer appearance and a significant reduction of tumor volume in the two groups of E6-immunized mice, thus confirming the pivotal role of the CD8(+) T-cell response in the control of tumor growth in the absence of E6-specific antibodies. In the therapeutic protocol, in-vivo experiments resulted in a higher number of tumor-free mice after the homologous DNA/DNA or heterologous DNA/FP immunization.

conclusionsThese data establish a preliminary indication for the prevention and treatment of HPV-related tumors by the use of DNA and avipox constructs as safe and effective immunogens following a prime/boost strategy. The combined use of recombinants expressing both E6 and E7 proteins might improve the antitumor efficacy, and should represent an important approach to control HPV-associated cancers.

Indexed as

Immunization, SecondaryAnimalsCancer VaccinesCD8-Positive T-LymphocytesChick EmbryoDNA, RecombinantFemaleFowlpoxHuman papillomavirus 16HumansImmunity, HumoralMice, Inbred C57BLNeoplasmsOncogene Proteins, ViralRepressor ProteinsTransgenesCancer VaccinesDNA, RecombinantE6 protein, Human papillomavirus type 16Oncogene Proteins, ViralRepressor Proteins

Identifiers

PMID25763880
PMCPMC4351974
OpenAlexW2150427979

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Registered trials

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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.