Author:
Esparcia-Pinedo Laura,Yarci-Carrión Ayla,Mateo-Jiménez Gloria,Ropero Noelia,Gómez-Cabañas Laura,Lancho-Sánchez Ángel,Martín-Gayo Enrique,Sanchez-Madrid Francisco,Moldenhauer Fernando,Gutiérrez-Cobos Ainhoa,de Asúa Diego Real,Alfranca Arantzazu
Abstract
ABSTRACTImmune dysregulation in individuals with Down syndrome (DS) leads to an increased risk for hospitalization and death due to COVID-19 and may impair the generation of protective immunity after vaccine administration. The cellular and humoral responses of 55 DS patients who received a complete SARS-CoV-2 vaccination regime at one to three (V1) and six (V2) months were characterised. SARS-CoV-2-reactive CD4+ and CD8+ T lymphocytes with a predominant Th1 phenotype were observed at V1, and increased at V2. Likewise, a sustained increase of SARS-CoV-2-specific circulating Tfh (cTfh) cells was observed one to three months after vaccine administration. Specific IgG antibodies against SARS-CoV-2 S protein were detected in 96% and 98% of subjects at V1 and V2, respectively, though IgG titers decreased significantly between both timepoints.SUMMARYThe work shows the cellular and humoral responses to SARS-CoV-2 vaccination of individuals with Down syndrome (DS) after one to three (V1) and six (V2) months. An effective immune response after six months was observed in 98% of DS individuals.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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