Opportunities to improve immune-based prevention of HPV-associated cancers

Immunization of adolescent girls with VLP vaccines, made of L1 proteins from the most medically significant high risk HPV types, is a major strategy for prevention of cervical cancer plus other HPV-associated cancers. Maximal population impact, including through herd immunity, requires high vaccinat...

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Main Authors: Peter L. Stern, Richard BS. Roden
Format: Article
Language:English
Published: Elsevier 2019-06-01
Series:Papillomavirus Research
Online Access:http://www.sciencedirect.com/science/article/pii/S2405852119300084
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spelling doaj-0b5f02836e1443d7bc93d4f142a226612020-11-25T01:40:28ZengElsevierPapillomavirus Research2405-85212019-06-017150153Opportunities to improve immune-based prevention of HPV-associated cancersPeter L. Stern0Richard BS. Roden1Division of Molecular & Clinical Cancer Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, Manchester Cancer Research Centre, University of Manchester, Wilmslow Road, Manchester, M20 4BX, United Kingdom; Corresponding author.Department of Pathology, Johns Hopkins University, 1550 Orleans St, Baltimore, MD, 21287, USAImmunization of adolescent girls with VLP vaccines, made of L1 proteins from the most medically significant high risk HPV types, is a major strategy for prevention of cervical cancer plus other HPV-associated cancers. Maximal population impact, including through herd immunity, requires high vaccination coverage. However, protection of unvaccinated women requires secondary prevention through cytology screening. Unfortunately in countries with the highest incidence/mortality due to cervical cancer HPV vaccination (or cytology screening) is not sufficiently available. Vaccination programme costs and a lack of accessibility of the populations for immunization remain significant hurdles. Several approaches could increase effective implementation of HPV vaccination. 1) Use of a single immunization of the current VLP vaccines. 2) Vaccination bundled with other paediatric vaccines with lower dosage to facilitate delivery, improve coverage and reduce costs through established logistics. 3) Local manufacture with lower cost systems (e.g. bacteria) for VLP or capsomer based vaccine production and utilization of additional protective epitopes (e.g L2) for increasing breadth of protection. However, all the latter need appropriate clinical validation. Gender neutral vaccination and extending routine vaccination strategies to women up to age 30 years in combination with at least one HPV screening test can also hasten impact on cancer incidence. Keywords: Virus like protein, Vaccination population coverage, Paediatric vaccination, Immune correlates of protection, Herd immunity, Therapeutic vaccinehttp://www.sciencedirect.com/science/article/pii/S2405852119300084
collection DOAJ
language English
format Article
sources DOAJ
author Peter L. Stern
Richard BS. Roden
spellingShingle Peter L. Stern
Richard BS. Roden
Opportunities to improve immune-based prevention of HPV-associated cancers
Papillomavirus Research
author_facet Peter L. Stern
Richard BS. Roden
author_sort Peter L. Stern
title Opportunities to improve immune-based prevention of HPV-associated cancers
title_short Opportunities to improve immune-based prevention of HPV-associated cancers
title_full Opportunities to improve immune-based prevention of HPV-associated cancers
title_fullStr Opportunities to improve immune-based prevention of HPV-associated cancers
title_full_unstemmed Opportunities to improve immune-based prevention of HPV-associated cancers
title_sort opportunities to improve immune-based prevention of hpv-associated cancers
publisher Elsevier
series Papillomavirus Research
issn 2405-8521
publishDate 2019-06-01
description Immunization of adolescent girls with VLP vaccines, made of L1 proteins from the most medically significant high risk HPV types, is a major strategy for prevention of cervical cancer plus other HPV-associated cancers. Maximal population impact, including through herd immunity, requires high vaccination coverage. However, protection of unvaccinated women requires secondary prevention through cytology screening. Unfortunately in countries with the highest incidence/mortality due to cervical cancer HPV vaccination (or cytology screening) is not sufficiently available. Vaccination programme costs and a lack of accessibility of the populations for immunization remain significant hurdles. Several approaches could increase effective implementation of HPV vaccination. 1) Use of a single immunization of the current VLP vaccines. 2) Vaccination bundled with other paediatric vaccines with lower dosage to facilitate delivery, improve coverage and reduce costs through established logistics. 3) Local manufacture with lower cost systems (e.g. bacteria) for VLP or capsomer based vaccine production and utilization of additional protective epitopes (e.g L2) for increasing breadth of protection. However, all the latter need appropriate clinical validation. Gender neutral vaccination and extending routine vaccination strategies to women up to age 30 years in combination with at least one HPV screening test can also hasten impact on cancer incidence. Keywords: Virus like protein, Vaccination population coverage, Paediatric vaccination, Immune correlates of protection, Herd immunity, Therapeutic vaccine
url http://www.sciencedirect.com/science/article/pii/S2405852119300084
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