Image
Image_1_Serial infection with SARS-CoV-2 Omicron BA.1 and BA.2 following three-dose COVID-19 vaccination.tiff
| العنوان: | Image_1_Serial infection with SARS-CoV-2 Omicron BA.1 and BA.2 following three-dose COVID-19 vaccination.tiff |
|---|---|
| المؤلفون: | Hope R. Lapointe, Francis Mwimanzi, Peter K. Cheung, Yurou Sang, Fatima Yaseen, Rebecca Kalikawe, Sneha Datwani, Rachel Waterworth, Gisele Umviligihozo, Siobhan Ennis, Landon Young, Winnie Dong, Don Kirkby, Laura Burns, Victor Leung, Daniel T. Holmes, Mari L. DeMarco, Janet Simons, Nancy Matic, Julio S.G. Montaner, Chanson J. Brumme, Natalie Prystajecky, Masahiro Niikura, Christopher F. Lowe, Marc G. Romney, Mark A. Brockman, Zabrina L. Brumme |
| سنة النشر: | 2022 |
| المجموعة: | Frontiers: Figshare |
| مصطلحات موضوعية: | Immunology, Applied Immunology (incl. Antibody Engineering, Xenotransplantation and T-cell Therapies), Autoimmunity, Cellular Immunology, Humoural Immunology and Immunochemistry, Immunogenetics (incl. Genetic Immunology), Innate Immunity, Transplantation Immunology, Tumour Immunology, Immunology not elsewhere classified, Genetic Immunology, Animal Immunology, Veterinary Immunology, COVID-19, vaccine, Omicron variant, reinfection, humoral immunity |
| الوصف: | SARS-CoV-2 Omicron infections are common among individuals who are vaccinated or have recovered from prior variant infection, but few reports have immunologically assessed serial Omicron infections. We characterized SARS-CoV-2 humoral responses in an individual who acquired laboratory-confirmed Omicron BA.1.15 ten weeks after a third dose of BNT162b2, and BA.2 thirteen weeks later. Responses were compared to 124 COVID-19-naive vaccinees. One month post-second and -third vaccine doses, the participant’s wild-type and BA.1-specific IgG, ACE2-displacement and virus neutralization activities were average for a COVID-19-naive triple-vaccinated individual. BA.1 infection boosted the participant’s responses to the cohort ≥95th percentile, but even this strong “hybrid” immunity failed to protect against BA.2. Reinfection increased BA.1 and BA.2-specific responses only modestly. Though vaccines clearly protect against severe disease, results highlight the continued importance of maintaining additional protective measures to counteract the immune-evasive Omicron variant, particularly as vaccine-induced immune responses naturally decline over time. |
| نوع الوثيقة: | still image |
| اللغة: | unknown |
| Relation: | https://figshare.com/articles/figure/Image_1_Serial_infection_with_SARS-CoV-2_Omicron_BA_1_and_BA_2_following_three-dose_COVID-19_vaccination_tiff/20964427 |
| DOI: | 10.3389/fimmu.2022.947021.s001 |
| الاتاحة: | https://doi.org/10.3389/fimmu.2022.947021.s001 https://figshare.com/articles/figure/Image_1_Serial_infection_with_SARS-CoV-2_Omicron_BA_1_and_BA_2_following_three-dose_COVID-19_vaccination_tiff/20964427 |
| Rights: | CC BY 4.0 |
| رقم الانضمام: | edsbas.F44376B5 |
| قاعدة البيانات: | BASE |
| DOI: | 10.3389/fimmu.2022.947021.s001 |
|---|