Evidence map›Paper›PMID 12239317›Full record

ArticleJournal of virology2002

Life cycle heterogeneity in animal models of human papillomavirus-associated disease.

Woei Ling Peh, Kate Middleton, Neil Christensen, Philip Nicholls, Kiyofumi Egawa, Karl Sotlar, Janet Brandsma, Alan Percival, Jon Lewis, Wen Jun Liu and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 1 pooled it
5.5field-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

87 citing papers in PubMed, 1 synthesis or guideline pooled it, 179 citations in OpenAlex.

  1. Pooled it
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  3. Review
  4. Characterization of Three Novel Papillomavirus Genomes in Vampire Bats (Animals : an open access journal from MDPI · 2024
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27 more citing papers are in PubMed but not listed here.

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

11 authors at 7 institutions in 5 countries.

Woei Ling PehNational Institute for Medical Research, The Ridgeway, Mill Hill, London NW7 1AA, UK.
Kate Middleton
Neil Christensen
Philip Nicholls
Kiyofumi Egawa
Karl Sotlar
Janet Brandsma
Alan Percival
Jon Lewis
Wen Jun Liu
John Doorbar
National Institute for Medical Research · TZKumamoto University · JPMurdoch University · AUPenn State Milton S. Hershey Medical Center · USRoche (United Kingdom) · GBThe University of Queensland · AUYale University · US

Funding

Medical Research Council MC_U117584278
6 · The paper itself

Abstract

Animal papillomaviruses are widely used as models to study papillomavirus infection in humans despite differences in genome organization and tissue tropism. Here, we have investigated the extent to which animal models of papillomavirus infection resemble human disease by comparing the life cycles of 10 different papillomavirus types. Three phases in the life cycles of all viruses were apparent using antibodies that distinguish between early events, the onset of viral genome amplification, and the expression of capsid proteins. The initiation of these phases follows a highly ordered pattern that appears important for the production of virus particles. The viruses examined included canine oral papillomavirus, rabbit oral papillomavirus (ROPV), cottontail rabbit papillomavirus (CRPV), bovine papillomavirus type 1, and human papillomavirus types 1, 2, 11, and 16. Each papillomavirus type showed a distinctive gene expression pattern that could be explained in part by differences in tissue tropism, transmission route, and persistence. As the timing of life cycle events affects the accessibility of viral antigens to the immune system, the ideal model system should resemble human mucosal infection if vaccine design is to be effective. Of the model systems examined here, only ROPV had a tissue tropism and a life cycle organization that resembled those of the human mucosal types. ROPV appears most appropriate for studies of the life cycles of mucosal papillomavirus types and for the development of prophylactic vaccines. The persistence of abortive infections caused by CRPV offers advantages for the development of therapeutic vaccines.

Indexed as

Capsid ProteinsAnimalsAntigens, ViralBovine papillomavirus 1CapsidCottontail rabbit papillomavirusDisease Models, AnimalGenes, ViralHumansOncogene Proteins, ViralPapillomaviridaePapillomavirus InfectionsRabbitsTime FactorsTumor Virus InfectionsViral Structural ProteinsAntigens, ViralCapsid ProteinsL1 protein, canine oral papillomavirusL1 protein, cottontail rabbit papillomavirusL1 protein, Human papillomavirus type 11oncogene protein E4, Human papillomavirus type 16oncogene protein E4, type 11, Human papillomavirusOncogene Proteins, ViralViral Structural Proteins

Identifiers

PMID12239317
PMCPMC136551
OpenAlexW2136856855

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.