Development of Neutralizing Monoclonal Antibodies for Oncogenic Human Papillomavirus Types 31, 33, 45, 52, and 58

被引:21
作者
Brown, Martha J. [1 ]
Seitz, Hanna [2 ]
Towne, Victoria [1 ]
Mueller, Martin [2 ]
Finnefrock, Adam C. [1 ]
机构
[1] Merck Res Labs, West Point, PA USA
[2] Deutsch Krebsforschungszentrum, Heidelberg, Germany
关键词
VIRUS-LIKE PARTICLES; GARDASIL(R); REACTIVITY; L1; CLASSIFICATION; PSEUDOVIRIONS; INFECTION; EPITOPES; WOMEN; ASSAY;
D O I
10.1128/CVI.00773-13
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human papillomavirus (HPV) is the etiological agent for all cervical cancers, a significant number of other anogenital cancers, and a growing number of head and neck cancers. Two licensed vaccines offer protection against the most prevalent oncogenic types, 16 and 18, responsible for approximately 70% of cervical cancer cases worldwide and one of these also offers protection against types 6 and 11, responsible for 90% of genital warts. The vaccines are comprised of recombinantly expressed major capsid proteins that self-assemble into virus-like particles (VLPs) and prevent infection by eliciting neutralizing antibodies. Adding the other frequently identified oncogenic types 31, 33, 45, 52, and 58 to a vaccine would increase the coverage against HPV-induced cancers to approximately 90%. We describe the generation and characterization of panels of monoclonal antibodies to these five additional oncogenic HPV types, and the selection of antibody pairs that were high affinity and type specific and recognized conformation-dependent neutralizing epitopes. Such characteristics make these antibodies useful tools for monitoring the production and potency of a prototype vaccine as well as monitoring vaccine-induced immune responses in the clinic.
引用
收藏
页码:587 / 593
页数:7
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