Evidence map›Paper›PMID 25152769›Full record

ArticleInfectious agents and cancer2014

Co-infection with HPV types from the same species provides natural cross-protection from progression to cervical cancer.

Rafal S Sobota, Doreen Ramogola-Masire, Scott M Williams, Nicola M Zetola

Abstract read
In one paragraph

Article in Infectious agents and cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. 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

4 authors.

Rafal S SobotaCenter for Human Genetics Research, Department of Molecular Physiology and Biophysics, Vanderbilt University Medical Center, Nashville, TN, USA ; Department of Genetics, Geisel School of Medicine, Dartmouth College, Hanover, NH, USA ; Center for Human Genetics Research, Vanderbilt University, 519 Light Hall, 2215 Garland AveNashville, TN 37232, USA.
Doreen Ramogola-MasireDivision of Infectious Disease, University of Pennsylvania, Philadelphia, PA, USA ; Botswana-University of Pennsylvania Partnership, 214 Independence Ave, Gaborone, Botswana ; Department of Medicine, University of Botswana, Gaborone, Botswana.
Scott M WilliamsDepartment of Genetics, Geisel School of Medicine, Dartmouth College, Hanover, NH, USA.
Nicola M ZetolaDivision of Infectious Disease, University of Pennsylvania, Philadelphia, PA, USA ; Botswana-University of Pennsylvania Partnership, 214 Independence Ave, Gaborone, Botswana ; Department of Medicine, University of Botswana, Gaborone, Botswana.

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007347 · NIGMS · VANDERBILT UNIVERSITY · PI WILLIAMS, CHRISTOPHER S. · 1985 to 2023
$26.3M
NIGMS NIH HHS T32 GM007347
6 · The paper itself

Abstract

backgroundThe worldwide administration of bivalent and quadrivalent HPV vaccines has resulted in cross-protection against non-vaccine HPV types. Infection with multiple HPV types may offer similar cross-protection in the natural setting. We hypothesized that infections with two or more HPV types from the same species, and independently, infections with two or more HPV types from different species, associate with protection from high-grade lesions.

findingsWe recruited a cohort of 94 HIV, HPV-positive women from Botswana, with Grade 2 or higher cervical intraepithelial neoplasia. Infections with 2 or more HPV types from a single species associated with reduced lesion severity in univariate analysis (OR = 0.41, 95% CI 0.18-0.97, p = 0.042), when adjusted for the presence of HPV 16 or 18 types (OR = 0.41, 95% CI 0.17-1.00, p = 0.049), or all high-risk HPV type infections (OR = 0.38, 95% CI 0.16-0.90, p = 0.028). Infections with 2 or more HPV types from different species did not associate (OR = 0.68, 95% CI 0.25-1.81, p = 0.435).

conclusionsOur findings show that co-infections with genetically similar HPV types reduce the likelihood of progression to high-grade lesions in HIV positive women, an effect not observed in co-infections with taxonomically different HPV types. This observation is possibly caused by an immune cross-protection through a similar mechanism to that observed after HPV vaccination.

Indexed as

Cervical cancerCoinfectionHPVImmune cross-protectionTaxonomyVaccine

Identifiers

PMID25152769
PMCPMC4141127

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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.