Evaluation of serological assays to monitor antibody responses to single-dose HPV vaccines.


Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
27 08 2020
Historique:
received: 21 04 2020
revised: 02 07 2020
accepted: 10 07 2020
pubmed: 28 7 2020
medline: 28 4 2021
entrez: 28 7 2020
Statut: ppublish

Résumé

Whether existing serological assays are sufficiently robust to measure the lower antibody levels expected following single-dose HPV vaccination is unknown. We evaluated seven assays measuring HPV-16/18 immunological responses overall and by number of doses in 530 serum samples from participants receiving varying doses of Cervarix or Gardasil up to 36-months post-vaccination. Serum was evaluated by simplex (HPV-16 ELISA, HPV-18 ELISA), multiplex (LIA-4, VLP-MIA, M9ELISA, GST-L1), and high-throughput pseudovirion-based neutralization assays (HT-PBNA), and results were compared to the gold standard HPV-16/18 secreted alkaline phosphatase neutralization assay (SEAP-NA). Reproducibility was assessed by the coefficient of variation (CV) and intraclass correlation coefficient (ICC). Percent agreement, Pearson correlation, and weighted-kappa were used to assess validity. Determinants of seronegativity were evaluated by chi-squared test. HPV-16: Seropositivity range was 97.1-99.5% for single dose and 98.8-99.8% overall. CV range was 4.0-18.0% for single dose and 2.9-19.5% overall. ICC range was 0.77-0.99 for single dose and 0.74-0.99 overall. Correlation with SEAP-NA range was 0.43-0.85 for single dose and 0.51-0.90 overall. Weighted-kappa range was 0.34-0.82 for single dose and 0.45-0.84 overall. HPV-18: Seropositivity range was 63.9-94.7% for single dose and 86.2-97.9% overall. CV range was 8.1-18.2% for single dose and 4.6-18.6% overall. ICC range was 0.75-0.99 for single dose and 0.83-0.99 overall. Correlation with SEAP-NA range was 0.31-0.99 for single dose and 0.27-0.96 overall. Weighted-kappa range was 0.35-0.83 for single dose and 0.45-0.84 overall. HPV-16 seronegativity was <5% for all assays. HPV-18 seronegativity range was 5.5-17.3%. For LIA-4 and GST-L1 where the proportion of seronegativity was >10%, the strongest correlates of seronegativity were receiving a single vaccine dose and receiving Gardasil. These results support the utility of existing serological assays to monitor antibody responses following single-dose HPV vaccination.

Identifiants

pubmed: 32713678
pii: S0264-410X(20)30917-8
doi: 10.1016/j.vaccine.2020.07.017
pmc: PMC7429278
mid: NIHMS1611643
pii:
doi:

Substances chimiques

Antibodies, Viral 0
Human Papillomavirus Recombinant Vaccine Quadrivalent, Types 6, 11, 16, 18 0
Papillomavirus Vaccines 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5997-6006

Subventions

Organisme : NCI NIH HHS
ID : N01CP11005
Pays : United States
Organisme : Intramural NIH HHS
ID : Z01 CP010177
Pays : United States

Informations de copyright

Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Sabrina H Tsang (SH)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Partha Basu (P)

Screening Group, International Agency for Research on Cancer, Lyon, France.

Noemi Bender (N)

Infection, Inflammation & Cancer Program, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Rolando Herrero (R)

Agencia Costarricense de Investigaciones Biomédicas (ACIB), formerly Proyecto Epidemiológico Guanacaste, Fundación INCIENSA, San José, Costa Rica.

Troy J Kemp (TJ)

HPV Immunology Laboratory, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, MD, USA.

Aimée R Kreimer (AR)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Martin Müller (M)

Infection, Inflammation & Cancer Program, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Gitika Panicker (G)

Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, GA, USA.

Michael Pawlita (M)

Infection, Inflammation & Cancer Program, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Ligia A Pinto (LA)

HPV Immunology Laboratory, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, MD, USA.

Joshua N Sampson (JN)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Rengaswamy Sankaranarayanan (R)

Research Triangle Institute International, New Delhi, India.

John Schussler (J)

Information Management Services, Silver Spring, MD, USA.

Peter Sehr (P)

Infection, Inflammation & Cancer Program, German Cancer Research Center (DKFZ), Heidelberg, Germany; Chemical Biology Core Facility, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.

Monica S Sierra (MS)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Elizabeth R Unger (ER)

Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, GA, USA.

Tim Waterboer (T)

Infection, Inflammation & Cancer Program, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Allan Hildesheim (A)

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA. Electronic address: Hildesha@mail.nih.gov.

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Classifications MeSH