Anti-Cancer Vaccine for HPV-Associated Neoplasms: Focus on a Therapeutic HPV Vaccine Based on a Novel Tumor Antigen Delivery Method Using Endogenously Engineered Exosomes

被引:26
|
作者
Di Bonito, Paola [1 ]
Accardi, Luisa [1 ]
Galati, Luisa [1 ]
Ferrantelli, Flavia [2 ]
Federico, Maurizio [2 ]
机构
[1] Ist Super Sanita, Dept Infect Dis, Viral Hepatitis Oncoviruses & Retroviruses EVOR U, Viale Regina Elena 299, I-00161 Rome, Italy
[2] Ist Super Sanita, Natl Ctr Global Hlth, Viale Regina Elena 299, I-00161 Rome, Italy
关键词
cancer immunotherapy; HPV16; therapeutic vaccines; extracellular vesicles; exosomes; cytotoxic T lymphocytes; PAPILLOMAVIRUS TYPE-16 E6; INTRAEPITHELIAL NEOPLASIA; IMMUNE CHECKPOINTS; FUSION PROTEIN; DNA VACCINES; CANCER; VIRUS; IMMUNOGENICITY; COMBINATION; EFFICACY;
D O I
10.3390/cancers11020138
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Some human papillomavirus (HPV) genotypes are universally recognized as major etiological agents not only of ano-genital tumors but also of head and neck cancers, which show increasing incidence. The evaluation of current and future therapeutic approaches against HPV-induced tumors is a global health priority, despite an effective prophylactic vaccine against 7 of the 12 genotypes involved in the etiology of tumors being currently available. In this review, we present the main anti-HPV therapeutic approaches in clinical experimentation, with a focus on a novel tumor antigen delivery method using engineered exosomes, that we recently developed. Our system allows the induction of an efficient unrestricted cytotoxic T lymphocyte (CTL) immune response against the HPV16-E7 tumor-associated antigen, with the formation of endogenously engineered exosomes, i.e., nanovesicles spontaneously released by all cell types. Immunogenic exosomes are uploaded with HPV16-E7 due to the fusion with a unique exosome-anchoring protein referred to as Nef(mut). Intramuscular injection of a DNA vector expressing the fusion protein generates exosomes sufficiently immunogenic to elicit a potent anti-16E7 CTL immune response. The approach is described here and the advantages over other existing methodologies are reported.
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页数:15
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