PAPILLOMAVIRUS-LIKE PARTICLES FOR SEROLOGY AND VACCINE DEVELOPMENT

Authors
Citation
R. Kirnbauer, PAPILLOMAVIRUS-LIKE PARTICLES FOR SEROLOGY AND VACCINE DEVELOPMENT, Intervirology, 39(1-2), 1996, pp. 54-61
Citations number
82
Categorie Soggetti
Virology
Journal title
ISSN journal
03005526
Volume
39
Issue
1-2
Year of publication
1996
Pages
54 - 61
Database
ISI
SICI code
0300-5526(1996)39:1-2<54:PPFSAV>2.0.ZU;2-N
Abstract
Genital infection with high-risk human papillomaviruses (HPV) has been etiologically linked with the development of cervical and other anoge nital cancers. There is therefore a need for an effective HPV vaccine with the potential to significantly reduce the burden of more than hal f a million new cervical cancer cases in women worldwide each year. Th e L1 major capsid protein of papillomaviruses expressed in eukaryotic cells self-assembles into virus-like particles (VLP). VLP are attracti ve subunit vaccine candidates since they lack potentially oncogenic pa pillomavirus DNA and express the conformationally dependent epitopes n ecessary to induce high-titer neutralizing antibodies. Prophylactic VL P vaccination has achieved a high degree of protection in animal studi es. Thus VLP are now considered the immunogen of choice for human vacc ine trials to prevent genital HPV infection. VLP of different HPV have been developed to study the serologic relationship between HPV types. VLP-based ELISA are able to detect antibodies in human sera and are n ow widely used in epidemiologic studies of the natural history of HPV infection and the associated risk of developing neoplasia.