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Cutting Edge: Effect of Disease-Modifying Therapies on SARS-CoV-2 Vaccine-Induced Immune Responses in Multiple Sclerosis Patients.
Yuzefpolskiy, Yevgeniy; Morawski, Peter; Fahning, Mitch; Speake, Cate; Lord, Sandra; Chaudhary, Anu; Morishima, Chihiro; Wener, Mark H; Kita, Mariko; McCarthy, Lucas; Buckner, Jane H; Campbell, Daniel J; Bettelli, Estelle.
Affiliation
  • Yuzefpolskiy Y; Center for Fundamental Immunology, Benaroya Research Institute at Virginia Mason, Seattle, WA.
  • Morawski P; Center for Fundamental Immunology, Benaroya Research Institute at Virginia Mason, Seattle, WA.
  • Fahning M; Center for Fundamental Immunology, Benaroya Research Institute at Virginia Mason, Seattle, WA.
  • Speake C; Center for Interventional Immunology, Benaroya Research Institute at Virginia Mason, Seattle, WA.
  • Lord S; Center for Interventional Immunology, Benaroya Research Institute at Virginia Mason, Seattle, WA.
  • Chaudhary A; Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA.
  • Morishima C; Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA.
  • Wener MH; Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA.
  • Kita M; Department of Medicine, University of Washington School of Medicine, Seattle, WA.
  • McCarthy L; Neuroscience Institute, Virginia Mason Medical Center, Seattle, WA.
  • Buckner JH; Neuroscience Institute, Virginia Mason Medical Center, Seattle, WA.
  • Campbell DJ; Translational Research Program, Benaroya Research Institute at Virginia Mason, Seattle, WA; and.
  • Bettelli E; Center for Fundamental Immunology, Benaroya Research Institute at Virginia Mason, Seattle, WA.
J Immunol ; 208(7): 1519-1524, 2022 04 01.
Article in En | MEDLINE | ID: mdl-35288472
Multiple sclerosis (MS) is a demyelinating inflammatory disease of the CNS treated by diverse disease-modifying therapies that suppress the immune system. Severe acute respiratory syndrome coronavirus 2 mRNA vaccines have been very effective in immunocompetent individuals, but whether MS patients treated with modifying therapies are afforded the same protection is not known. This study determined that dimethyl fumarate caused a momentary reduction in anti-Spike (S)-specific Abs and CD8 T cell response. MS patients treated with B cell-depleting (anti-CD20) or sphingosine 1-phosphate receptor agonist (fingolimod) therapies lack significant S-specific Ab response. Whereas S-specific CD4 and CD8 T cell responses were largely compromised by fingolimod treatment, T cell responses were robustly generated in anti-CD20-treated MS patients, but with a reduced proportion of CD4+CXCR5+ circulating follicular Th cells. These data provide novel information regarding vaccine immune response in patients with autoimmunity useful to help improve vaccine effectiveness in these populations.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: COVID-19 / Multiple Sclerosis Limits: Humans Language: En Journal: J Immunol Year: 2022 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: COVID-19 / Multiple Sclerosis Limits: Humans Language: En Journal: J Immunol Year: 2022 Document type: Article Country of publication: