It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
While mRNA vaccines are administrated worldwide in an effort to contain the COVID-19 pandemic, the heterogeneity of the humoral immune response they induce at the population scale remains unclear. Here, in a prospective, longitudinal, cohort-study, including 1245 hospital care workers and 146 nursing home residents scheduled for BNT162b2 vaccination, together covering adult ages from 19 to 99 years, we analyse seroconversion to SARS-CoV-2 spike protein and amount of spike-specific IgG, IgM and IgA before vaccination, and 3-5 weeks after each dose. We show that immunogenicity after a single vaccine dose is biased to IgG, heterogeneous and reduced with increasing age. The second vaccine dose normalizes IgG seroconversion in all age strata. These findings indicate two dose mRNA vaccines is required to reach population scale humoral immunity. The results advocate for the interval between the two doses not to be extended, and for serological monitoring of elderly and immunosuppressed vaccinees.
Here, in a longitudinal cohort of 1245 hospital care workers and 146 nursing home residents, the authors find that a large inter-individual variation in anti-spike antibody levels after one dose of BNT162b2mRNA vaccine is partially explained by age, sex, previous exposure, and treatments, while the 2nd dose is required to reach sero-conversion at the population level.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details
; Bergman Marie-Louise 2
; Gonçalves, Lígia A 2 ; Duarte Nádia 2
; Coutinho, Teresa P 3
; Borges, Patrícia C 2 ; Diwo Christian 2 ; Castro Rute 4
; Matoso Paula 2 ; Malheiro Vanessa 2 ; Brennand, Ana 2 ; Kosack Lindsay 2
; Onome, Akpogheneta 2 ; Figueira, João M 5 ; Cardoso Conceição 5 ; Casaca, Ana M 5 ; Alves, Paula M 6
; Nunes Telmo 3
; Penha-Gonçalves, Carlos 2
; Demengeot Jocelyne 2
1 CHLO, Centro Hospitalar de Lisboa Ocidental, Serviço de Patologia Clínica, Lisbon, Portugal
2 IGC, Instituto Gulbenkian de Ciência, Oeiras, Portugal (GRID:grid.418346.c) (ISNI:0000 0001 2191 3202)
3 University of Lisbon, CIISA, Centre for Interdisciplinary Research in Animal Health, Faculty of Veterinary Medicine, Lisbon, Portugal (GRID:grid.9983.b) (ISNI:0000 0001 2181 4263)
4 IBET, Instituto de Biologia Experimental e Tecnológica, Oeiras, Portugal (GRID:grid.7665.2)
5 CHLO, Centro Hospitalar de Lisboa Ocidental, Serviço de Patologia Clínica, Lisbon, Portugal (GRID:grid.418346.c)
6 IBET, Instituto de Biologia Experimental e Tecnológica, Oeiras, Portugal (GRID:grid.7665.2); Universidade Nova de Lisboa, ITQB NOVA, Instituto de Tecnológia Química e Biológica António Xavier, Oeiras, Portugal (GRID:grid.10772.33) (ISNI:0000000121511713)




