dc.date.accessioned | 2023-12-05T17:48:01Z | |
dc.date.accessioned | 2024-04-24T13:25:58Z | |
dc.date.available | 2023-12-05T17:48:01Z | |
dc.date.available | 2024-04-24T13:25:58Z | |
dc.date.created | 2023-12-05T17:48:01Z | |
dc.date.issued | 2023 | |
dc.identifier | https://hdl.handle.net/20.500.12866/14643 | |
dc.identifier | https://doi.org/10.1126/science.adj0070 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/9231871 | |
dc.description.abstract | During the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic, multiple variants escaping preexisting immunity emerged, causing reinfections of previously exposed individuals. Here, we used antigenic cartography to analyze patterns of cross-reactivity among 21 variants and 15 groups of human sera obtained after primary infection with 10 different variants or after messenger RNA (mRNA)–1273 or mRNA-1273.351 vaccination. We found antigenic differences among pre-Omicron variants caused by substitutions at spike-protein positions 417, 452, 484, and 501. Quantifying changes in response breadth over time and with additional vaccine doses, our results show the largest increase between 4 weeks and >3 months after a second dose. We found changes in immunodominance of different spike regions, depending on the variant an individual was first exposed to, with implications for variant risk assessment and vaccine-strain selection. | |
dc.language | eng | |
dc.publisher | American Association for the Advancement of Science | |
dc.relation | Science | |
dc.relation | 1095-9203 | |
dc.rights | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.subject | SARS-CoV-2 | |
dc.subject | Antigenic | |
dc.subject | Serological | |
dc.title | Mapping SARS-CoV-2 antigenic relationships and serological responses | |
dc.type | info:eu-repo/semantics/article | |