Evidence map›Paper›PMID 40600436›Full record

ArticleJournal of medical virology2025

IgG and IgM Seroreactivity Against Natural HPV16 Infection and HLA-DRB1 and -DQB1 Polymorphism.

Letícia Boslooper Gonçalves, Andrea Trevisan, Eduardo L Franco, Luisa L Villa, Helen Trottier, Patrícia Savio de Araujo-Souza, Ludwig‐McGill Study Group

Abstract read
In one paragraph

Article in Journal of medical virology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Letícia Boslooper GonçalvesPost-Graduation Program in Genetics, Department of Genetics, Universidade Federal do Paraná (UFPR), Curitiba, Brazil.ORCID https://orcid.org/0000-0002-6144-5471
Andrea TrevisanSainte-Justine Hospital Research Center, Université de Montréal, Montreal, Canada.ORCID https://orcid.org/0000-0002-6890-0713
Eduardo L FrancoDivision of Cancer Epidemiology, McGill University, Montreal, Canada.ORCID https://orcid.org/0000-0002-4409-8084
Luisa L VillaInstituto do Cancer do Estado de São Paulo, Universidade de São Paulo, Sao Paulo, Brazil.ORCID https://orcid.org/0000-0003-4074-2335
Helen TrottierSainte-Justine Hospital Research Center, Université de Montréal, Montreal, Canada.ORCID https://orcid.org/0000-0003-3293-7837
Patrícia Savio de Araujo-SouzaLaboratory of Immunogenetics and Histocompatibility, Department of Genetics, Universidade Federal do Paraná (UFPR), Curitiba, Brazil.ORCID https://orcid.org/0000-0002-4489-9148
Ludwig‐McGill Study Group

Funding

MOLECULAR EPIDEMIOLOGY OF PERSISTENT HPV INFECTIONR01CA070269 · NCI · MCGILL UNIVERSITY · PI FRANCO, EDUARDO L. · 1996 to 2003
$793k
NCI NIH HHS R01 CA070269This study was supported by Ludwig Institute for Cancer Research to E.F. and L.V.; the U.S. National Cancer Institute [CA70269 to E.F.] and the Canadian Institutes of Health Research [MOP-49396, CRN-83320 to E.F.]; The Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) provided a scholarship to LBG (protocol number: 141955/2020-1) and a fellowship to PSAS (protocol number 311540/2022-8). CAPES/Print-UFPR provided a scholarship to LBG during her staying in Canada (CAPES/Print-UFPR protocol number: 88887.840291/2023-00).
6 · The paper itself

Abstract

Little is known about the factors associated with the natural humoral immune response against human papillomavirus (HPV) infection. The association between HLA-DRB1 and -DQB1 polymorphism and (1) HPV16 DNA detection, (2) naturally developed humoral immune response (IgG and IgM) against HPV16 L1 and L2 capsid proteins, and (3) type of HPV16 infection (transient or persistent) was investigated. Data from 943 women participating in the Ludwig-McGill cohort study was analyzed. HLA-DRB1 and HLA-DQB1 genotyping was done by PCR-based methods. HPV DNA was assessed every 4 months during the first year of follow-up, and HPV16 IgG and IgM antibody measurements were performed by ELISA in serum samples from the first and/or second visits. Associations were estimated by adjusted logistic regression models. HLA-DRB1*03:02 was associated with HPV16 DNA positivity (OR = 2.49, 95% CI: 1.11-5.60). HLA-DRB1*13:01 and HLA-DQB1*04:02 were associated with low levels of HPV16 IgG antibodies (OR = 0.44, 95% CI:0.23-0.87; OR = 0.10, 95% CI: 0.02-0.55, respectively). Neither IgM HPV16 antibodies nor the type of HPV16 infection (transient or persistent) were associated with HLA-DRB1 or -DQB1 variants. HLA-DRB1 and -DQB1 polymorphism might be associated with different levels of IgG against HPV16 infection, but IgM production and the type of infection seem to occur independently of these variants.

Indexed as

Antibodies, ViralHLA-DQ beta-ChainsHLA-DRB1 ChainsHuman papillomavirus 16Immunoglobulin GImmunoglobulin MPapillomavirus InfectionsPolymorphism, GeneticAdultCapsid ProteinsCohort StudiesDNA, ViralFemaleGenotypeHumansMiddle AgedAntibodies, ViralCapsid ProteinsDNA, ViralHLA-DQB1 antigenHLA-DQ beta-ChainsHLA-DRB1 ChainsImmunoglobulin GImmunoglobulin MOncogene Proteins, ViralantibodyHLA polymorphismHPV16IgGIgM

Identifiers

PMID40600436
PMCPMC12216804

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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.