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ABSTRACT: Background
Immune 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.Methods
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 characterized.Results
SARS-CoV-2-reactive CD4 + and CD8+ T lymphocytes with a predominant Th1 phenotype were observed at V1 and increased at V2. Likewise, an increase of SARS-CoV-2-specific circulating Tfh (cTfh) cells and CD8+ CXCR5+ PD-1hi lymphocytes were already observed at V1 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.Conclusions
Our findings show that DS individuals develop an effective immune response to usual regimes of SARS-CoV-2 vaccination.
SUBMITTER: Esparcia-Pinedo L
PROVIDER: S-EPMC9384526 | biostudies-literature | 2022 Jul
REPOSITORIES: biostudies-literature
Esparcia-Pinedo Laura L Yarci-Carrión Ayla A Mateo-Jiménez Gloria G Ropero Noelia N Gómez-Cabañas Laura L Lancho-Sánchez Ángel Á Almendro-Vázquez Patricia P Martín-Gayo Enrique E Paz-Artal Estela E Sanchez-Madrid Francisco F Moldenhauer Fernando F Gutiérrez-Cobos Ainhoa A Real de Asúa Diego D Alfranca Arantzazu A
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 20230201 3
<h4>Background</h4>Immune dysregulation in individuals with Down syndrome (DS) leads to an increased risk for hospitalization and death due to coronavirus disease 2019 (COVID-19) and may impair the generation of protective immunity after vaccine administration.<h4>Methods</h4>The cellular and humoral responses of 55 individuals with DS who received a complete SARS-CoV-2 vaccination regime at 1 to 3 (visit [V 1]) and 6 (V2) months were characterized.<h4>Results</h4>SARS-CoV-2-reactive CD4+ and CD ...[more]