Literature DB >> 14711335

Preventative and therapeutic vaccines for cervical cancer.

Richard Roden1, T-C Wu.   

Abstract

"High-risk" genotypes of the human papillomavirus (HPV), most commonly HPV genotype 16, are the primary etiologic agents of cervical cancer. Indeed HPV DNA is detected in 99% of cervical carcinomas. Thus, cervical cancer and other HPV-associated malignancies might be prevented or treated by the induction of the appropriate viral-antigen-specific immune responses. Transmission of papillomavirus may be prevented by the generation of antibodies to capsid proteins L1 and L2 that neutralize viral infection. HPV L1 virus-like particles (VLPs) show great promise as prophylactic HPV vaccines in ongoing clinical trials but L2-based preventative vaccines have yet to be tested in patients. Since the capsid proteins are not expressed at detectable levels by infected basal keratinocytes or in HPV-transformed cells, therapeutic vaccines generally target the nonstructural early viral antigens. Two HPV oncogenic proteins, E6 and E7, are critical to the induction and maintenance of cellular transformation and are co-expressed in the majority of HPV-containing carcinomas. Although other early viral antigens show promise for vaccination against papillomas, therapeutic vaccines targeting E6 and E7 may provide the best opportunity to control HPV-associated malignancies. Various candidate therapeutic HPV vaccines are currently being tested whereby E6 and/or E7 are administered in live vectors, as peptides or proteins, in nucleic acid form, as components of chimeric VLPs, or in cell-based vaccines. Encouraging results from experimental vaccination systems in animal models have led to several prophylactic and therapeutic vaccine clinical trials. Should this new generation of HPV preventative and therapeutic vaccines function in patients as demonstrated in animal models, oncogenic HPV infection and its associated malignancies could be controlled by vaccination. Importantly, recent advances in HPV detection and continued improvements in screening further enhance our opportunities to systematically eradicate HPV-associated malignancy.

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Year:  2003        PMID: 14711335     DOI: 10.1586/14760584.2.4.495

Source DB:  PubMed          Journal:  Expert Rev Vaccines        ISSN: 1476-0584            Impact factor:   5.217


  7 in total

1.  HPV pseudovirions as DNA delivery vehicles.

Authors:  Barbara Ma; Richard B S Roden; Chien-Fu Hung; T C Wu
Journal:  Ther Deliv       Date:  2011-04

2.  Control of cervicovaginal HPV-16 E7-expressing tumors by the combination of therapeutic HPV vaccination and vascular disrupting agents.

Authors:  Qi Zeng; Shiwen Peng; Archana Monie; Ming Yang; Xiaowu Pang; Chien-Fu Hung; T-C Wu
Journal:  Hum Gene Ther       Date:  2011-03-09       Impact factor: 5.695

3.  Human papillomavirus vaccine update.

Authors:  Alisa Ames; Patti Gravitt
Journal:  Curr Infect Dis Rep       Date:  2007-03       Impact factor: 3.725

4.  Low-dose radiation enhances therapeutic HPV DNA vaccination in tumor-bearing hosts.

Authors:  Chih-Wen Tseng; Cornelia Trimble; Qi Zeng; Archana Monie; Ronald D Alvarez; Warner K Huh; Talia Hoory; Mei-Cheng Wang; Chien-Fu Hung; T-C Wu
Journal:  Cancer Immunol Immunother       Date:  2008-09-25       Impact factor: 6.968

5.  Efficient delivery of DNA vaccines using human papillomavirus pseudovirions.

Authors:  S Peng; A Monie; T H Kang; C-F Hung; R Roden; T-C Wu
Journal:  Gene Ther       Date:  2010-07-29       Impact factor: 5.250

6.  Induction of antitumor immunity in vivo following delivery of a novel HPV-16 DNA vaccine encoding an E6/E7 fusion antigen.

Authors:  Jian Yan; Dawn K Reichenbach; Natasha Corbitt; David A Hokey; Mathura P Ramanathan; Kibwei A McKinney; David B Weiner; Duane Sewell
Journal:  Vaccine       Date:  2008-11-18       Impact factor: 3.641

Review 7.  Virus-like particles: passport to immune recognition.

Authors:  Elizabeth V L Grgacic; David A Anderson
Journal:  Methods       Date:  2006-09       Impact factor: 3.608

  7 in total

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