共 2 条
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
来源:
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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