Evidence map›Paper›PMID 30121951›Full record

ArticleInternational journal of cancer2018

Toll-like receptors: Important immune checkpoints in the regression of cervical intra-epithelial neoplasia 2.

Gordana Halec, Mark E Scott, Sepideh Farhat, Teresa M Darragh, Anna-Barbara Moscicki

Open access · bronzeAbstract read
In one paragraph

Article in International journal of cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed, 35 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Gordana HalecDivision of Adolescent Medicine, Department of Pediatrics, University of California, Los Angeles, CA.ORCID 0000-0002-3772-7401
Mark E ScottDepartment of Pediatrics, University of California, San Francisco, CA.
Sepideh FarhatDepartment of Pediatrics, University of California, San Francisco, CA.
Teresa M DarraghDepartment of Pathology, University of California, San Francisco, CA.
Anna-Barbara MoscickiDivision of Adolescent Medicine, Department of Pediatrics, University of California, Los Angeles, CA.ORCID 0000-0002-6317-5233
University of California, San Francisco · USUniversity of California, Los Angeles · US

Funding

Natural History of HPV Infection to NeoplasiaR37CA051323 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MOSCICKI, ANNA-BARBARA · 2005 to 2014
$15.4M
NATURAL HISTORY OF HPV IN TEENS--INFECTION TO NEOPLASIAR01CA051323 · NCI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI MOSCICKI, ANNA-BARBARA NONE · 1990 to 2004
$6.0M
Natural History of CIN2 in AdolescentsR01CA087905 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MOSCICKI, ANNA-BARBARA · 2001 to 2007
$3.9M
National Institutes of Health (NIH) R01 CA87905NCI NIH HHS R01 CA051323NCI NIH HHS R01 CA087905NCI NIH HHS R37 CA051323
6 · The paper itself

Abstract

Toll-like receptors (TLRs) are innate immune defenders thought to be critical for the clearance of human papillomavirus (HPV) infections hence preventing the development of HPV-associated high-grade cervical intra-epithelial neoplasia (CIN2 or 3), a potential cervical cancer precursor. However, the role of TLRs in the regression of established cervical lesions, such as CIN2, is hindered by a lack of prospective design studies. Using SYBR green real-time PCR assays, we have examined the gene expression of TLR2, TLR3, TLR7, TLR8 and TLR9, in cytobrush collected endocervical cells of 63 women diagnosed with CIN2 at study entry (baseline) and followed over a 3-year period. Wilcoxon rank-sum test was used to examine the association between TLR expression levels, measured at baseline, and CIN2 outcome (regression vs. persistence/progression) over time. HPV genotyping was performed using Roche Linear Array Assay detecting 37 HPV types. Women with CIN2 regression showed significantly higher baseline levels of TLR2 (p = 0.006) and TLR7 (p = 0.007), as well as a non-significant trend for a higher TLR8 expression (p = 0.053) compared to women with CIN2 persistence/progression. Six women with CIN2 regression, who presented with an HR-HPV DNA-negative CIN2 lesion at study entry, had significantly higher baseline levels of TLR2 (p = 0.005), TLR7 (p = 0.013) and TLR8 (p = 0.012), compared to women with CIN2 persistence/progression, suggesting their role in clearance of HPV prior to clearance of the lesion. Our results confirm a key role of TLRs in regression of CIN2 and support the potential use of TLR-agonists for treatment of these lesions.

Indexed as

AdolescentAdultCervix UteriFemaleHumansPapillomaviridaePapillomavirus InfectionsToll-Like ReceptorsUterine Cervical DysplasiaUterine Cervical NeoplasmsVaginal SmearsYoung AdultToll-Like Receptorscervical intra-epithelial neoplasia 2CIN2 regressionhuman papillomavirusToll-like receptors

Identifiers

PMID30121951
PMCPMC6419742
OpenAlexW2886417518

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.