The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) posed a threat to public health and the global economy, necessitating the development of various vaccination strategies. Mutations in the SPIKE protein gene, a crucial component of mRNA and adenovirus-based vaccines, raised concerns about vaccine efficacy, prompting the need for rapid vaccine updates. To address this, we leveraged PeptiCRAd, an oncolytic vaccine based on tumor antigen decorated oncolytic adenoviruses, creating a vaccine platform called PeptiVAX . First, we identified multiple CD8 T -cell epitopes from highly conserved regions across coronaviruses, expanding the range of T -cell responses to non -SPIKE proteins. We designed short segments containing the predicted epitopes presented by common HLA-Is in the global population. Testing the immunogenicity, we characterized T -cell responses to candidate peptides in peripheral blood mononuclear cells (PBMCs) from prepandemic healthy donors and ICU patients. As a proof of concept in mice, we selected a peptide with epitopes predicted to bind to murine MHC-I haplotypes. Our technology successfully elicited peptide -specific T -cell responses, unaffected by the use of unarmed adenoviral vectors or adeno-based vaccines encoding SPIKE.

PeptiVAX: A new adaptable peptides-delivery platform for development of CTL-based, SARS-CoV-2 vaccines / Feola, Sara; Chiaro, Jacopo; Fusciello, Manlio; Russo, Salvatore; Kleino, Iivari; Ylösmäki, Leena; Kekäläinen, Eliisa; Hästbacka, Johanna; Pekkarinen, Pirkka T.; Ylösmäki, Erkko; Capone, Stefania; Folgori, Antonella; Raggioli, Angelo; Boni, Carolina; Tiezzi, Camilla; Vecchi, Andrea; Gelzo, Monica; Kared, Hassen; Nardin, Alessandra; Fehlings, Michael; Barban, Veronique; Ahokas, Petra; Viitala, Tapani; Castaldo, Giuseppe; Pastore, Lucio; Porter, Paul; Pesonen, Sari; Cerullo, Vincenzo. - In: INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES. - ISSN 0141-8130. - 262:Pt 1(2024). [10.1016/j.ijbiomac.2024.129926]

PeptiVAX: A new adaptable peptides-delivery platform for development of CTL-based, SARS-CoV-2 vaccines

Boni, Carolina;Tiezzi, Camilla;
2024-01-01

Abstract

The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) posed a threat to public health and the global economy, necessitating the development of various vaccination strategies. Mutations in the SPIKE protein gene, a crucial component of mRNA and adenovirus-based vaccines, raised concerns about vaccine efficacy, prompting the need for rapid vaccine updates. To address this, we leveraged PeptiCRAd, an oncolytic vaccine based on tumor antigen decorated oncolytic adenoviruses, creating a vaccine platform called PeptiVAX . First, we identified multiple CD8 T -cell epitopes from highly conserved regions across coronaviruses, expanding the range of T -cell responses to non -SPIKE proteins. We designed short segments containing the predicted epitopes presented by common HLA-Is in the global population. Testing the immunogenicity, we characterized T -cell responses to candidate peptides in peripheral blood mononuclear cells (PBMCs) from prepandemic healthy donors and ICU patients. As a proof of concept in mice, we selected a peptide with epitopes predicted to bind to murine MHC-I haplotypes. Our technology successfully elicited peptide -specific T -cell responses, unaffected by the use of unarmed adenoviral vectors or adeno-based vaccines encoding SPIKE.
2024
PeptiVAX: A new adaptable peptides-delivery platform for development of CTL-based, SARS-CoV-2 vaccines / Feola, Sara; Chiaro, Jacopo; Fusciello, Manlio; Russo, Salvatore; Kleino, Iivari; Ylösmäki, Leena; Kekäläinen, Eliisa; Hästbacka, Johanna; Pekkarinen, Pirkka T.; Ylösmäki, Erkko; Capone, Stefania; Folgori, Antonella; Raggioli, Angelo; Boni, Carolina; Tiezzi, Camilla; Vecchi, Andrea; Gelzo, Monica; Kared, Hassen; Nardin, Alessandra; Fehlings, Michael; Barban, Veronique; Ahokas, Petra; Viitala, Tapani; Castaldo, Giuseppe; Pastore, Lucio; Porter, Paul; Pesonen, Sari; Cerullo, Vincenzo. - In: INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES. - ISSN 0141-8130. - 262:Pt 1(2024). [10.1016/j.ijbiomac.2024.129926]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/2983413
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