Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Advertisement

Experimental & Molecular Medicine
  • View all journals
  • Search
  • My Account Login
  • Content Explore content
  • About the journal
  • Publish with us
  • Sign up for alerts
  • RSS feed
  1. nature
  2. experimental & molecular medicine
  3. review
  4. article
DNA vaccines for cervical cancer: from bench to bedside
Download PDF
Download PDF
  • Review
  • Open access
  • Published: 01 December 2007

DNA vaccines for cervical cancer: from bench to bedside

  • Chien-Fu Hung1,
  • Archana Monie,
  • Ronald D Alvarez &
  • …
  • T-C Wu 

Experimental & Molecular Medicine volume 39, pages 679–689 (2007)Cite this article

  • 1781 Accesses

  • 59 Citations

  • 6 Altmetric

  • Metrics details

Abstract

More than 99% of cervical cancers have been associated with human papillomaviruses (HPVs), particularly HPV type 16. The clear association between HPV infection and cervical cancer indicates that HPV serves as an ideal target for development of preventive and therapeutic vaccines. Although the recently licensed preventive HPV vaccine, Gardasil, has been shown to be safe and capable of generating significant protection against specific HPV types, it does not have therapeutic effect against established HPV infections and HPV-associated lesions. Two HPV oncogenic proteins, E6 and E7, are consistently co-expressed in HPV-expressing cervical cancers and are important in the induction and maintenance of cellular transformation. Therefore, immunotherapy targeting E6 and/or E7 proteins may provide an opportunity to prevent and treat HPV-associated cervical malignancies. It has been established that T cell-mediated immunity is one of the most crucial components to defend against HPV infections and HPV-associated lesions. Therefore, effective therapeutic HPV vaccines should generate strong E6/E7-specific T cell-mediated immune responses. DNA vaccines have emerged as an attractive approach for antigen-specific T cell-mediated immunotherapy to combat cancers. Intradermal administration of DNA vaccines via a gene gun represents an efficient way to deliver DNA vaccines into professional antigen-presenting cells in vivo. Professional antigen-presenting cells, such as dendritic cells, are the most effective cells for priming antigen-specific T cells. Using the gene gun delivery system, we tested several DNA vaccines that employ intracellular targeting strategies for enhancing MHC class I and class II presentation of encoded model antigen HPV-16 E7. Furthermore, we have developed a strategy to prolong the life of DCs to enhance DNA vaccine potency. More recently, we have developed a strategy to generate antigen-specific CD4+ T cell immune responses to further enhance DNA vaccine potency. The impressive pre- clinical data generated from our studies have led to several HPV DNA vaccine clinical trials.

Similar content being viewed by others

A safe and potentiated multi-type HPV L2-E7 nanoparticle vaccine with combined prophylactic and therapeutic activity

Article Open access 26 June 2024

Virus against virus: strategies for using adenovirus vectors in the treatment of HPV-induced cervical cancer

Article 25 February 2021

Mathematical modelling of the role of Langerhans cells in the dynamics of HPV infection

Article Open access 20 May 2025

Article PDF

Author information

Authors and Affiliations

  1. Department of Pathology, Johns Hopkins Medical Institutions Baltimore, MD, 21231, USA

    Chien-Fu Hung

Authors
  1. Chien-Fu Hung
    View author publications

    Search author on:PubMed Google Scholar

  2. Archana Monie
    View author publications

    Search author on:PubMed Google Scholar

  3. Ronald D Alvarez
    View author publications

    Search author on:PubMed Google Scholar

  4. T-C Wu
    View author publications

    Search author on:PubMed Google Scholar

Rights and permissions

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Hung, CF., Monie, A., Alvarez, R. et al. DNA vaccines for cervical cancer: from bench to bedside. Exp Mol Med 39, 679–689 (2007). https://doi.org/10.1038/emm.2007.74

Download citation

  • Published: 01 December 2007

  • Issue date: 01 December 2007

  • DOI: https://doi.org/10.1038/emm.2007.74

Share this article

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

Keywords

  • antigen presenting cells
  • dendritic cells
  • human papillomavirus type 16
  • oncogene protein E7
  • papillomavirus vaccines
  • vaccination
  • vaccines, DNA

This article is cited by

  • A phase 1, single centre, open label, escalating dose study to assess the safety, tolerability and immunogenicity of a therapeutic human papillomavirus (HPV) DNA vaccine (AMV002) for HPV-associated head and neck cancer (HNC)

    • J. Chandra
    • W. P. Woo
    • Sandro V. Porceddu

    Cancer Immunology, Immunotherapy (2021)

  • Current status and future prospects for human papillomavirus vaccines

    • Hyoung Jin Kim
    • Hong-Jin Kim

    Archives of Pharmacal Research (2017)

  • Human papillomavirus: current status and issues of vaccination

    • Heena Malik
    • Fahim H. Khan
    • Haseeb Ahsan

    Archives of Virology (2014)

  • Enhancing DNA vaccine potency by co-administration of xenogenic MHC class-I DNA

    • T H Kang
    • J-Y Chung
    • T-C Wu

    Gene Therapy (2010)

Download PDF

Advertisement

Explore content

  • Research articles
  • Reviews & Analysis
  • News & Comment
  • Current issue
  • Collections
  • Sign up for alerts
  • RSS feed

About the journal

  • Special Feature
  • Journal Information
  • About the Editors
  • About the Partner
  • Contact
  • For Advertisers
  • Press Releases
  • Open Access Fees and Funding

Publish with us

  • For Authors & Referees
  • Language editing services
  • Submit manuscript

Search

Advanced search

Quick links

  • Explore articles by subject
  • Find a job
  • Guide to authors
  • Editorial policies

Experimental & Molecular Medicine (Exp Mol Med)

ISSN 2092-6413 (online)

ISSN 1226-3613 (print)

nature.com sitemap

About Nature Portfolio

  • About us
  • Press releases
  • Press office
  • Contact us

Discover content

  • Journals A-Z
  • Articles by subject
  • protocols.io
  • Nature Index

Publishing policies

  • Nature portfolio policies
  • Open access

Author & Researcher services

  • Reprints & permissions
  • Research data
  • Language editing
  • Scientific editing
  • Nature Masterclasses
  • Research Solutions

Libraries & institutions

  • Librarian service & tools
  • Librarian portal
  • Open research
  • Recommend to library

Advertising & partnerships

  • Advertising
  • Partnerships & Services
  • Media kits
  • Branded content

Professional development

  • Nature Awards
  • Nature Careers
  • Nature Conferences

Regional websites

  • Nature Africa
  • Nature China
  • Nature India
  • Nature Japan
  • Nature Middle East
  • Privacy Policy
  • Use of cookies
  • Legal notice
  • Accessibility statement
  • Terms & Conditions
  • Your US state privacy rights
Springer Nature

© 2025 Springer Nature Limited