Table 1

Study subject characteristics

SARD (n=82)HC (n=82)
Age, mean (SD)52.0 (±14.1)52.1 (±13.4)
Female, n (%)65 (79)65 (79)
Systemic lupus erythematosus, n (%)33 (40)
Systemic sclerosis, n (%)13 (16)
Other connective tissue diseases*, n (%)15 (18)
Vasculitides†, n (%)17 (21)
Miscellaneous‡, n (%)4 (5)
csDMARD or b/tsDMARD monotherapy, n (%)43 (52)
csDMARD and/or b/tsDMARD combination therapy§, n (%)16 (20)
No therapy, n (%)23 (28)
Methotrexate (monotherapy or combination), n (%)13 (16)
Mycophenolate (monotherapy or combination), n (%)14 (17)
Hydroxychloroquine (monotherapy or combination), n (%)28 (34)
Azathioprine (monotherapy or combination), n (%)13 (10)
Belimumab (monotherapy or combination), n (%)3 (4)
Tocilizumab (monotherapy or combination), n (%)3 (4)
Tacrolimus (monotherapy or combination), n (%)2 (2)
Olumiant (monotherapy or combination), n (%)1 (1)
Glucocorticoid dose at first vaccination, mean (SD)2.5 (±9.4)
Glucocorticoid dose at second vaccination, mean (SD)2.2 (±9.2)
  • *Dermatomyositis/polymyositis (n=4), mixed connective tissue disease (n=2), primary Sjögren’s syndrome (n=6) and undifferentiated connective tissue disease (n=3).

  • †Antineutrophil cytoplasmic antibody-associated vasculitis (n=3), Behcet’s disease (n=1), large-vessel vasculitis (n=3) and polymyalgia rheumatica (n=10).

  • ‡Adult-onset Still’s disease (n=1), immune deficiency (n=2) and sarcoidosis (n=1).

  • §Azathioprine+hydroxychloroquine (n=6), mycophenolate+hydroxychloroquine (n=5), azathioprine+belimumab (n=1), belimumab+hydroxychloroquine (n=1), mycophenolate+tacrolimus (n=1), azathioprine+belimumab+hydroxychloroquine (n=1), and mycophenolate+hydroxychloroquine+tacrolimus (n=1).

  • b/tsDMARD, biological/targeted synthetic disease-modifying antirheumatic drug; csDMARD, conventional synthetic disease-modifying antirheumatic drug; HC, healthy control; SARD, systemic autoimmune rheumatic disease.