AI Article Synopsis

  • Certain HPV genotypes are linked to both ano-genital and head and neck cancers, and while there's a vaccine for some genotypes, therapeutic strategies against HPV-related tumors are still a priority.
  • The review highlights new therapeutic methods, particularly a novel approach involving engineered exosomes that deliver tumor antigens, specifically targeting the HPV16-E7 antigen.
  • This innovative system generates a strong immune response by using a DNA vector to create immunogenic exosomes, which could surpass current treatment methodologies.

Article Abstract

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. 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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406600PMC
http://dx.doi.org/10.3390/cancers11020138DOI Listing

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