IMR Press / FBL / Volume 8 / Issue 6 / DOI: 10.2741/1003

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on as a courtesy and upon agreement with Frontiers in Bioscience.

A review of human papillomavirus vaccines: from basic science to clinical trials
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1 University of California, San Francisco, Box 0512, 521 Parnassus Ave., San Francisco, CA 94143-0512, USA
2 General Clinical Research Center, Box 0126, 505 Parnassus Ave, Room M1203, University of California, San Francisco, San Francisco CA 94143

Academic Editor: Erle Robertson

Front. Biosci. (Landmark Ed) 2003, 8(6), 333–345;
Published: 1 May 2003
(This article belongs to the Special Issue DNA viruses and human malignancies)

Human papillomavirus (HPV) infection leads to a spectrum of disease from genital warts to precancerous lesions to cervical and anal cancer and is a worldwide public health problem of epidemic proportions. Unique to HPV-related neoplasia, the presence of specific viral antigens such as the L1 capsid structural protein and the oncoproteins E6 and E7 provide opportunities for vaccine therapy. Although difficult to precisely define, the natural immune response to HPV is vitally important and defects in cell mediated immunity correlate with increased risk of disease and cancer. In preclinical animal models, both prophylactic and therapeutic vaccines have effectively induced HPV-specific cell mediated immune responses protecting animals from viral challenge or eliminating established tumors. Most prophylactic vaccines are virus-like particles (VLP) composed of the L1 structural protein. Phase I trials have demonstrated safety and immunogenicity, but limited efficacy data are available. Therapeutic vaccine trials are reviewed including E6 and E7 vaccines comprised of peptides, fusion proteins, encapsulated plasmid DNA, and recombinant vaccinia virus. All of the vaccines appear to be safe, well tolerated, and preliminary data indicates that most are clinically effective. Multiple trials are in progress and more mature data are expected within the next few years.

Human Papillomavirus Vaccines
Anogenital Neoplasia
Squamous Intraepithelial Lesion
Anal Cancer
Cervical Cancer
Virus-Like Particle
Plasmid DNA Vaccine
Heat Shock Protein
Fusion Protein
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