Reassuring humoral and cellular immune responses to SARS-CoV-2 vaccination in participants with systemic sclerosis

Individuals with systemic sclerosis (SSc) are particularly susceptible to SARS-CoV-2 infections, yet it remains to be determined if they generate humoral and cellular responses comparable to controls following SARS-CoV-2 vaccinations. Herein, we collected blood and serum after second, third, and fourth SARS-CoV-2 vaccinations in patients with SSc and controls. Following each dose, participants with SSc mounted comparable serum anti-RBD IgG, anti-RBD IgA, and spike-specific CD4<sup>+</sup> and CD8<sup>+</sup>T cell responses to those found in controls. At 3 months post dose 2, the frequencies of Th1, Th2, Th17, and Treg spike-specific CD4<sup>+</sup>T cells in participants with SSc did not differ from controls. At 2-6 weeks post dose 3, participants with SSc displayed reduced frequencies, but not numbers, of Th17-polarized spike-specific CD4<sup>+</sup>T cells. Thus, participants with SSc did not display significantly weaker humoral or cellular responses to SARS-CoV-2 vaccination than controls, enabling reassurance of vaccine immunogenicity in participants with SSc.

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Publication Details

Journal
Immunology Letters
Published
2024-09-19
DOI
https://doi.org/10.1016/j.imlet.2024.106929
Primary Topic
Systemic Sclerosis and Related Diseases
Type
article
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article

Reassuring humoral and cellular immune responses to SARS-CoV-2 vaccination in participants with systemic sclerosis

Barbara Baker, Hina Bhakta, Sumiya Lodhi, Jessica A. Breznik et al.
Immunology Letters
Systemic Sclerosis and Related Diseases
article

Reassuring humoral and cellular immune responses to SARS-CoV-2 vaccination in participants with systemic sclerosis

Barbara Baker, Hina Bhakta, Sumiya Lodhi, Jessica A. Breznik, Rumi Clare, Dawn M. E. Bowdish, Elizabeth Yan, Braeden Cowbrough, Angela Huynh, Jenna M. Benoit, Maggie Larché, Jonathan L. Bramson, Ishac Nazy, Lauren Heessels
article en

Abstract

Individuals with systemic sclerosis (SSc) are particularly susceptible to SARS-CoV-2 infections, yet it remains to be determined if they generate humoral and cellular responses comparable to controls following SARS-CoV-2 vaccinations. Herein, we collected blood and serum after second, third, and fourth SARS-CoV-2 vaccinations in patients with SSc and controls. Following each dose, participants with SSc mounted comparable serum anti-RBD IgG, anti-RBD IgA, and spike-specific CD4<sup>+</sup> and CD8<sup>+</sup>T cell responses to those found in controls. At 3 months post dose 2, the frequencies of Th1, Th2, Th17, and Treg spike-specific CD4<sup>+</sup>T cells in participants with SSc did not differ from controls. At 2-6 weeks post dose 3, participants with SSc displayed reduced frequencies, but not numbers, of Th17-polarized spike-specific CD4<sup>+</sup>T cells. Thus, participants with SSc did not display significantly weaker humoral or cellular responses to SARS-CoV-2 vaccination than controls, enabling reassurance of vaccine immunogenicity in participants with SSc.

Immunology LettersVol. 270
University of Ottawa (CA), McMaster University Medical Centre (CA), St. Joseph’s Healthcare Hamilton (CA), McMaster University (CA)
Openalex Percentile: Top 75%
Systemic Sclerosis and Related Diseases
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