Current therapeutic vaccination and immunotherapy strategies for HPV-related diseases

被引:70
作者
Skeate, Joseph G. [1 ]
Woodham, Andrew W. [1 ]
Einstein, Mark H. [2 ]
Da Silva, Diane M. [3 ,4 ]
Kast, W. Martin [1 ,3 ,4 ]
机构
[1] Univ Southern Calif, Dept Mol Microbiol & Immunol, Los Angeles, CA USA
[2] Rutgers New Jersey Med Sch, Dept Obstet & Gynecol & Womens Hlth, Newark, NJ USA
[3] Univ Southern Calif, Dept Obstet & Gynecol, Los Angeles, CA USA
[4] Univ Southern Calif, Norris Comprehens Canc Ctr, Los Angeles, CA USA
关键词
anogenital cancers; cervical cancer; checkpoint inhibitors; head and neck cancer; human papillomavirus; immunotherapy; therapeutic vaccines; HUMAN-PAPILLOMAVIRUS TYPE-16; CERVICAL INTRAEPITHELIAL NEOPLASIA; T-CELL RESPONSES; PHASE-I TRIAL; DNA VACCINE; LANGERHANS CELLS; FUSION PROTEIN; CANCER PATIENTS; PRECANCEROUS LESIONS; UNITED-STATES;
D O I
10.1080/21645515.2015.1136039
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Carcinomas of the anogenital tract, in particular cervical cancer, remains one of the most common cancers in women, and represent the most frequent gynecological malignancies and the fourth leading cause of cancer death in women worldwide. Human papillomavirus (HPV)-induced lesions are immunologically distinct in that they express viral antigens, which are necessary to maintain the cancerous phenotype. The causal relationship between HPV infection and anogenital cancer has prompted substantial interest in the development of therapeutic vaccines against high-risk HPV types targeting the viral oncoproteins E6 and E7. This review will focus on the most recent clinical trials for immunotherapies for mucosal HPV-induced lesions as well as emerging therapeutic strategies that have been tested in pre-clinical models for HPV-induced diseases. Progress in peptide- and protein-based vaccines, DNA-based vaccines, viral/bacterial vector-based vaccines, immune checkpoint inhibition, immune response modifiers, and adoptive cell therapy for HPV will be discussed.
引用
收藏
页码:1418 / 1429
页数:12
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