Longitudinal assessment of nonavalent vaccine HPV types in a sample of sexually active African American women from ten U.S. Cities.


Journal

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

Informations de publication

Date de publication:
09 08 2021
Historique:
received: 29 11 2020
accepted: 11 07 2021
pubmed: 24 7 2021
medline: 14 8 2021
entrez: 23 7 2021
Statut: ppublish

Résumé

Chronic infection with high-risk human papillomavirus is a necessary cause for cervical carcinogenesis. This study examined prevalence of nonavalent vaccine preventable HPV types over four months among sexually active women in the United States. This sub-study obtained meta-data for 80 of the 1,365 women (18-25 years), enrolled in the BRAVO study, a randomized, open-label trial of home screening and treatment of asymptomatic bacterial vaginosis at high-risk for sexually transmitted infections conducted between 2008 and 2013. Participants were randomized to treatment or standard-of-care, and followed every 2-months for 12 months. Stored vaginal swabs from the first three visits were tested for the nine vaccine preventable HPV types using quantitative PCR. Prevalence and associated 95% confidence intervals for the HPV types were assessed using R (version 3.6.1). The average age of the participants was 21.5 (SD ± 2.11) years, with 60% having ever been pregnant and all were African-American. Majority (71%) reported ≥ two sex partners in the prior year with 89% having unprotected vaginal sex and 45% having a new sex partner in the prior year. About 30% had ≥ one of the nine nonavalent vaccine HPV types at all three time points over a period of four months, 15% at two of any three visits, 19% at one of the three visits and 36% were negative for all nine vaccine HPV types at all time points. The most frequently detected HPV vaccine types were 52, 58, 16, and 18. The prevalence of any vaccine HPV types, and high-risk HPV types was 63.8% and 58.8%, respectively. Our findings suggest that HPV vaccination which is currently recommended for all unvaccinated persons through age 26 years, is likely to be more beneficial than previously thought as nonavalent HPV vaccine was not available during the time these data were collected.

Sections du résumé

BACKGROUND
Chronic infection with high-risk human papillomavirus is a necessary cause for cervical carcinogenesis. This study examined prevalence of nonavalent vaccine preventable HPV types over four months among sexually active women in the United States.
METHODS
This sub-study obtained meta-data for 80 of the 1,365 women (18-25 years), enrolled in the BRAVO study, a randomized, open-label trial of home screening and treatment of asymptomatic bacterial vaginosis at high-risk for sexually transmitted infections conducted between 2008 and 2013. Participants were randomized to treatment or standard-of-care, and followed every 2-months for 12 months. Stored vaginal swabs from the first three visits were tested for the nine vaccine preventable HPV types using quantitative PCR. Prevalence and associated 95% confidence intervals for the HPV types were assessed using R (version 3.6.1).
RESULTS
The average age of the participants was 21.5 (SD ± 2.11) years, with 60% having ever been pregnant and all were African-American. Majority (71%) reported ≥ two sex partners in the prior year with 89% having unprotected vaginal sex and 45% having a new sex partner in the prior year. About 30% had ≥ one of the nine nonavalent vaccine HPV types at all three time points over a period of four months, 15% at two of any three visits, 19% at one of the three visits and 36% were negative for all nine vaccine HPV types at all time points. The most frequently detected HPV vaccine types were 52, 58, 16, and 18. The prevalence of any vaccine HPV types, and high-risk HPV types was 63.8% and 58.8%, respectively.
CONCLUSIONS
Our findings suggest that HPV vaccination which is currently recommended for all unvaccinated persons through age 26 years, is likely to be more beneficial than previously thought as nonavalent HPV vaccine was not available during the time these data were collected.

Identifiants

pubmed: 34294478
pii: S0264-410X(21)00903-8
doi: 10.1016/j.vaccine.2021.07.026
pmc: PMC8331072
mid: NIHMS1724358
pii:
doi:

Substances chimiques

Papillomavirus Vaccines 0
Vaccines, Combined 0

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

4810-4816

Subventions

Organisme : FIC NIH HHS
ID : D43 TW010540
Pays : United States
Organisme : NIAID NIH HHS
ID : R15 AI128714
Pays : United States

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

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.

Références

Clin Infect Dis. 2016 Mar 1;62(5):531-6
pubmed: 26611782
JNCI Cancer Spectr. 2019 Jan 07;2(4):pky045
pubmed: 31360870
Infect Dis (Auckl). 2019 Jan 28;12:1178633718825077
pubmed: 30728723
Pediatrics. 2014 Sep;134(3):e666-74
pubmed: 25136036
Viruses. 2017 Oct 10;9(10):
pubmed: 28994707
J Virol. 2018 Mar 28;92(8):
pubmed: 29437958
J Infect Dis. 2018 Aug 14;218(6):927-936
pubmed: 29850832
PLoS One. 2017 Nov 3;12(11):e0187193
pubmed: 29099839
J Adolesc Health. 2013 Dec;53(6):756-62
pubmed: 23992645
J Infect Dis. 2011 Aug 15;204(4):566-73
pubmed: 21791659
BMC Infect Dis. 2014 Jul 16;14:395
pubmed: 25030273
J Infect Dis. 2011 Mar 15;203(6):814-22
pubmed: 21343148
J Adolesc Health. 2010 Dec;47(6):596-9
pubmed: 21094437
J Infect Dis. 2015 Jan 15;211(2):172-4
pubmed: 25057043
Cancer Res. 2010 Nov 1;70(21):8569-77
pubmed: 20978200
J Infect Dis. 2014 Aug 1;210(3):448-55
pubmed: 24569064
Papillomavirus Res. 2020 Dec;10:100202
pubmed: 32464334
Vaccine. 2011 Jan 10;29(3):528-34
pubmed: 21050904
MMWR Morb Mortal Wkly Rep. 2019 Aug 16;68(32):698-702
pubmed: 31415491
Clin Infect Dis. 2018 Jun 18;67(1):73-79
pubmed: 29342269
Int J Cancer. 2013 Sep 15;133(6):1271-85
pubmed: 22961444
Hum Vaccin Immunother. 2019;15(1):146-155
pubmed: 30148974
Proc Natl Acad Sci U S A. 2017 Dec 19;114(51):13573-13578
pubmed: 29208707

Auteurs

P Madhivanan (P)

Mel & Enid Zuckerman College of Public Health, University of Arizona, Tucson, USA; College of Medicine, University of Arizona, Tucson, USA; University of Arizona Comprehensive Cancer Center, Tucson, USA. Electronic address: pmadhivanan@arizona.edu.

K Krupp (K)

Mel & Enid Zuckerman College of Public Health, University of Arizona, Tucson, USA; University of Arizona Comprehensive Cancer Center, Tucson, USA. Electronic address: kkrupp@arizona.edu.

M Coudray (M)

Robert Stempel College of Public Health and Social Work, Florida International University, Miami, USA; College of Medicine, University of Central Florida, Orlando, USA. Electronic address: Makella.Coudray@ucf.edu.

B Colbert (B)

Herbert Wertheim College of Medicine, Florida International University, Miami, USA. Electronic address: bmc48@miami.edu.

D Ruiz-Perez (D)

Bioinformatic Research Group (BioRG), School of Computing and Information Sciences, Florida International University, Miami, USA. Electronic address: druiz072@cs.fiu.edu.

H Cui (H)

University of Arizona Comprehensive Cancer Center, Tucson, USA. Electronic address: HCui@uacc.arizona.edu.

N Bokulich (N)

Laboratory of Food Systems Biotechnology, Institute of Food, Nutrition and Health, ETH Zurich, Switzerland. Electronic address: Nicholas.Bokulich@hest.ethz.ch.

G Narasimhan (G)

Herbert Wertheim College of Medicine, Florida International University, Miami, USA. Electronic address: giri@cs.fiu.edu.

K Mathee (K)

Herbert Wertheim College of Medicine, Florida International University, Miami, USA. Electronic address: matheek@fiu.edu.

R L Cook (RL)

College of Public Health and Health Professions, University of Florida, Gainesville, USA. Electronic address: cookrl@ufl.edu.

J Schwebke (J)

College of Medicine, University of Birmingham, Alabama, USA. Electronic address: janeschwebke@gmail.com.

D Roe (D)

Mel & Enid Zuckerman College of Public Health, University of Arizona, Tucson, USA; University of Arizona Comprehensive Cancer Center, Tucson, USA. Electronic address: droe@arizona.edu.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH