Skip to main content

Table 1 Demographic, diagnoses, disease characteristics, and treatment at inclusion in the study, in treatment groups and controls

From: Prime-boost vaccination strategy enhances immunogenicity compared to single pneumococcal conjugate vaccination in patients receiving conventional DMARDs, to some extent in abatacept but not in rituximab-treated patients

 

Rituximab

Abatacept

cDMARD1

Controls

N

30

23

27

28

Female gender, %

53%

83%

74%

64%

Age, median (range) years

69 (31–88)2

64 (42–78)2

68 (25–87)2

55 (18–84)

Rheumatoid arthritis, n (%)

27 (90%)

23 (100%)

14 (52%)

0

RF-positive (% of RA patients)

100%

79%

90%

Anti-CCP-positive (% of RA patients)

92%

68%

80%

Granulomatosis with polyangiitis, n (%)

3 (10%)

0

7 (26%)

0

Eosinophilic granulomatosis with polyangiitis, n (%)

0

0

3 (11%)

0

Other systemic vasculitis, n (%)

0

0

3 (11%)

0

Disease duration, median (range) years

20 (2–57)

15 (4–45)

5 (2–46)

DAS28 in RA patients, median (range)

2.7 (0.5–6.5)3

3.2 (1.5–5.5)

2.3 (1.6–4.3)

CRP, median mg/L

3.0

2.3

3.1

0.7

Total IgG, median (range) g/L

7.4 (4.0–13.9)

RTX duration, median (range) years

6.3 (0.7–10.9)

ABT duration, median (range) years

3.7 (0.7–10.2)

cDMARD duration, median (range) years

12.9 (3.3–22.4)

10.3 (4.2–20.3)

3.5 (1.4–15.3)

MTX, n (%)

16 (53%)

11 (48%)

19 (70%)

0

MTX mg/week, median

15

20

20

0

Azathioprine, n (%)

1 (3%)

0

5 (19%)

0

Azathioprine mg/day, median

150

0

100

0

Mycophenolate mofetil, n (%)

0

0

3 (11%)

0

Mycophenolate mofetil mg/day, median

0

0

1500

0

Prednisolone, n (%)

10 (33%)

10 (43%)

15 (56%)

0

Prednisolone mg/day, median (range)

5 (2.5–15)

5.6 (2.5–20)

5 (2.5–15)

0

Previous treatment with TNFα-inhibitor (%)

72.4

80.0

11.14

0

  1. 1Conventional disease-modifying antirheumatic drugs: methotrexate, azathioprine, or mycophenolate mofetil
  2. 2All treatment groups were older than controls (all p < 0.05)
  3. 3DAS28 did not differ between treatment groups
  4. 4In the cDMARD group, compared to other treatment groups, a lower proportion of patients had previously received TNFα-inhibitor treatment