COVID-19: S-Peptide RBD 484–508 Induces IFN-γ T-Cell Response in Naïve-to-Infection and Unvaccinated Subjects with Close Contact with SARS-CoV-2-Positive Patients

Despite the availability on the market of different anti-SARS-CoV-2 vaccines, there are still unanswered questions on whether they can stimulate long-lasting protection. A deep understanding of adaptive immune response to SARS-CoV-2 is important for optimizing both vaccine development and pandemic c...

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Veröffentlicht in:Viruses Jg. 15; H. 7; S. 1417
Hauptverfasser: Murdocca, Michela, Citro, Gennaro, Centanini, Eleonora, Giannini, Rosalinda, Latini, Andrea, Centofanti, Federica, Piano Mortari, Eva, Cocciadiferro, Dario, Novelli, Antonio, Bernardini, Sergio, Novelli, Giuseppe, Sangiuolo, Federica
Format: Journal Article
Sprache:Englisch
Veröffentlicht: Switzerland MDPI AG 22.06.2023
MDPI
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ISSN:1999-4915, 1999-4915
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Zusammenfassung:Despite the availability on the market of different anti-SARS-CoV-2 vaccines, there are still unanswered questions on whether they can stimulate long-lasting protection. A deep understanding of adaptive immune response to SARS-CoV-2 is important for optimizing both vaccine development and pandemic control measures. Among cytokines secreted by lymphocytes in response to viral infection, IFN-γ plays a pivotal role both in innate and adaptive immunity. In this study, we report on 28 naïve-to-SARS-Cov-2-infection and unvaccinated subjects, having reported a close and prolonged contact with COVID-19-positive patients. Samples were tested for defective genetic variants in interferon pathway genes by whole exome sequencing and anti-IFN autoantibodies production was investigated. Subject T-cells were cultured and infected with pseudotype particles bearing the S proteins and in parallel stimulated with two S-peptides designed on the RBD region of the spike protein. Our results showed that one of these peptides, RBD 484–508, induces a significant increase in IFN-γ gene expression and protein production in T-cells, comparable to those obtained in cells infected by SARS-CoV-2 pseudovirus. This work deepens our understanding of immune response and highlights the selected peptide as a reasonable approach to induce broad, potent, and variant concern-independent T-cell responses.
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ISSN:1999-4915
1999-4915
DOI:10.3390/v15071417