Advances in human papilloma virus vaccines: a patent review

被引:18
作者
Cho, Hee-Jeong [1 ]
Oh, Yu-Kyoung [1 ]
Kim, Young Bong [2 ,3 ]
机构
[1] Seoul Natl Univ, Coll Pharm, Seoul, South Korea
[2] Konkuk Univ, Coll Anim Biosci & Technol, Dept Anim Biotechnol, Seoul, South Korea
[3] KR Biotech Co, Seoul, South Korea
关键词
adjuvant system; cervical cancer; DNA vaccine; HPV; human papilloma virus; prophylactic vaccine; therapeutic vaccine; MAJOR CAPSID PROTEIN; MUCOADHESIVE DELIVERY-SYSTEMS; L1; PROTEIN; IMMUNE-RESPONSES; ESCHERICHIA-COLI; HPV VACCINES; SACCHAROMYCES-CEREVISIAE; CERVICAL-CARCINOMA; MUCOSAL VACCINES; EPITHELIAL-CELLS;
D O I
10.1517/13543776.2011.551114
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Introduction: Human papilloma virus (HPV) infection is the main factor associated with the development of cervical cancer. The currently available HPV vaccines, Gardasil (R) and Cervarix (R), can prevent infection by certain HPV types, but not all. At present, research efforts are being devoted to developing more broad spectrum preventative vaccines, as well as therapeutic vaccines. Areas covered: Recent advances in HPV vaccine development are reviewed in this paper, with a focus on worldwide patents and patent applications. In principle, patents that have been granted since 2002 are covered. Exceptions are the patents pending at PCT stage and recent patent applications since 2009. Readers will gain insights into the cutting-edge technologies being used in the development and production of vaccines, as well as adjuvant systems. Expert opinion: In the future, the use of mosaic virus-like particles (VLPs,) comprising at least one L1 protein of each HPV type, may be able to prevent infection by all HPV types while patented codon-optimization techniques and the use of edible or DNA-based vaccines may be good places to start for reducing costs. Future vaccines should ideally have both preventive and therapeutic efficacies. Enhanced immunogenicity could be achieved by the use of more effective adjuvants, such as nanoparticle-based delivery systems, or new classes of adjuvants.
引用
收藏
页码:295 / 309
页数:15
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