| Literature DB >> 35471956 |
Roya M Dayam1, Jaclyn C Law2, Rogier L Goetgebuer3, Gary Yc Chao2, Kento T Abe1,4, Mitchell Sutton5, Naomi Finkelstein5, Joanne M Stempak3, Daniel Pereira5, David Croitoru6, Lily Acheampong7, Saima Rizwan3, Klaudia Rymaszewski3, Raquel Milgrom3, Darshini Ganatra5, Nathalia V Batista2, Melanie Girard2, Irene Lau2, Ryan Law2, Michelle W Cheung2, Bhavisha Rathod1, Julia Kitaygorodsky1,4, Reuben Samson1,4, Queenie Hu1, W Rod Hardy1, Nigil Haroon5, Robert D Inman5, Vincent Piguet6,7, Vinod Chandran5,8, Mark S Silverberg1,3, Anne-Claude Gingras1,4, Tania H Watts2.
Abstract
BACKGROUNDLimited information is available on the impact of immunosuppressants on COVID-19 vaccination in patients with immune-mediated inflammatory diseases (IMID).METHODSThis observational cohort study examined the immunogenicity of SARS-CoV-2 mRNA vaccines in adult patients with inflammatory bowel disease, rheumatoid arthritis, ankylosing spondylitis, or psoriatic disease, with or without maintenance immunosuppressive therapies. Ab and T cell responses to SARS-CoV-2, including neutralization against SARS-CoV-2 variants, were determined before and after 1 and 2 vaccine doses.RESULTSWe prospectively followed 150 subjects, 26 healthy controls, 9 patients with IMID on no treatment, 44 on anti-TNF, 16 on anti-TNF with methotrexate/azathioprine (MTX/AZA), 10 on anti-IL-23, 28 on anti-IL-12/23, 9 on anti-IL-17, and 8 on MTX/AZA. Ab and T cell responses to SARS-CoV-2 were detected in all participants, increasing from dose 1 to dose 2 and declining 3 months later, with greater attrition in patients with IMID compared with healthy controls. Ab levels and neutralization efficacy against variants of concern were substantially lower in anti-TNF-treated patients than in healthy controls and were undetectable against Omicron by 3 months after dose 2.CONCLUSIONSOur findings support the need for a third dose of the mRNA vaccine and for continued monitoring of immunity in these patient groups.FUNDINGFunded by a donation from Juan and Stefania Speck and by Canadian Institutes of Health (CIHR)/COVID-Immunity Task Force (CITF) grants VR-1 172711 and VS1-175545 (to THW and ACG), CIHR FDN-143250 (to THW), GA2-177716 (to VC, ACG, and THW), and GA1-177703 (to ACG) and the CIHR rapid response network to SARS-CoV-2 variants, CoVaRR-Net (to ACG).Entities:
Keywords: Adaptive immunity; Autoimmune diseases; COVID-19; Immunology; Immunotherapy
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Year: 2022 PMID: 35471956 PMCID: PMC9220925 DOI: 10.1172/jci.insight.159721
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708