Exp Mol Med.
2007 Dec;39(6):679-689.
DNA vaccines for cervical cancer: from bench to bedside
- Affiliations
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- 1Department of Pathology, Johns Hopkins Medical Institutions Baltimore, MD 21231, USA. wutc@jhmi.edu
- 2Department of Oncology, Johns Hopkins Medical Institutions Baltimore, MD 21231, USA.
- 3Department of Obstetrics and Gynecology, Johns Hopkins Medical Institutions Baltimore, MD 21231, USA.
- 4Department of Molecular Microbiology and Immunology, Johns Hopkins Medical Institutions Baltimore, MD 21231, USA.
- 5Department of Gynecology and Obstetrics, University of Alabama at Birmingham, Birmingham, AL 35249, USA.
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.
Keyword
MeSH Terms
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Female
Humans
Oncogene Proteins, Viral/genetics/immunology
Papillomaviridae/*genetics/immunology
Papillomavirus Infections/immunology/*prevention & control
Papillomavirus Vaccines/*administration & dosage
Repressor Proteins
Uterine Cervical Neoplasms/*prevention & control
Vaccines, DNA/*administration & dosage
Viral Vaccines/administration & dosage
