Publication
De novo human angiotensin - converting enzyme 2 Decoy NL-CVX1 protects mice from severe disease after severe acute respiratory syndrome coronavirus 2 infection
dc.contributor.author | Rebelo, Maria | |
dc.contributor.author | Tang, Cong | |
dc.contributor.author | Coelho, Ana R. | |
dc.contributor.author | Labão-Almeida, Carlos | |
dc.contributor.author | Schneider, Matthias M. | |
dc.contributor.author | Tatalick, Laurie | |
dc.contributor.author | Ruivo, Pedro | |
dc.contributor.author | de Miranda, Marta Pires | |
dc.contributor.author | Gomes, Andreia | |
dc.contributor.author | Carvalho, Tânia | |
dc.contributor.author | Walker, Matthew J. | |
dc.contributor.author | Ausserwoeger, Hannes | |
dc.contributor.author | Simas, J. Pedro | |
dc.contributor.author | Veldhoen, Marc | |
dc.contributor.author | Knowles, Tuomas P. J. | |
dc.contributor.author | Silva, Daniel Adriano | |
dc.contributor.author | Shoultz, David | |
dc.contributor.author | Bernardes, Gonçalo J. L. | |
dc.date.accessioned | 2023-10-04T15:40:51Z | |
dc.date.available | 2023-10-04T15:40:51Z | |
dc.date.issued | 2023-09-15 | |
dc.description.abstract | The emergence of novel variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) underscores the need to investigate alternative approaches to prevent infection and treat patients with coronavirus disease 2019. Here, we report the preclinical efficacy of NL-CVX1, a de novo decoy that blocks virus entry into cells by binding with nanomolar affinity and high specificity to the receptor-binding domain of the SARS-CoV-2 spike protein. Using a transgenic mouse model of SARS-CoV-2 infection, we showed that a single prophylactic intranasal dose of NL-CVX1 conferred complete protection from severe disease following SARS-CoV-2 infection. Multiple therapeutic administrations of NL-CVX1 also protected mice from succumbing to infection. Finally, we showed that infected mice treated with NL-CVX1 developed both anti-SARS-CoV-2 antibodies and memory T cells and were protected against reinfection a month after treatment. Overall, these observations suggest NL-CVX1 is a promising therapeutic candidate for preventing and treating severe SARS-CoV-2 infections. | pt_PT |
dc.description.version | info:eu-repo/semantics/publishedVersion | pt_PT |
dc.identifier.eid | 85171601438 | |
dc.identifier.issn | 0022-1899 | |
dc.identifier.pmc | PMC10503951 | |
dc.identifier.pmid | 37279654 | |
dc.identifier.uri | http://hdl.handle.net/10400.14/42778 | |
dc.identifier.wos | 001002059700001 | |
dc.language.iso | eng | pt_PT |
dc.peerreviewed | yes | pt_PT |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | pt_PT |
dc.subject | COVID-19 | pt_PT |
dc.subject | De novo protein decoys | pt_PT |
dc.subject | K18-hACE2 mice | pt_PT |
dc.subject | SARS-CoV-2 | pt_PT |
dc.subject | Treatment | pt_PT |
dc.title | De novo human angiotensin - converting enzyme 2 Decoy NL-CVX1 protects mice from severe disease after severe acute respiratory syndrome coronavirus 2 infection | pt_PT |
dc.type | journal article | |
dspace.entity.type | Publication | |
oaire.citation.endPage | 733 | pt_PT |
oaire.citation.issue | 6 | pt_PT |
oaire.citation.startPage | 723 | pt_PT |
oaire.citation.title | The Journal of infectious diseases | pt_PT |
oaire.citation.volume | 228 | pt_PT |
rcaap.rights | openAccess | pt_PT |
rcaap.type | article | pt_PT |