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. 2014 Apr 24;176(3):410–417. doi: 10.1111/cei.12290

Table 1.

Baseline demographics and clinical characteristics of the three groups of patients at the time of blood collection for multi-functional analysis of T cells.

Characteristics Group A
(n = 12)
Group B
(n = 11)
Group C
(n = 10)
M/F (n) 5/7 7/4 4/6
Age (years; median/range) 63·5/21–76 45/36–71 58/30–75
Underlying disease (n/%)
 Rheumatoid arthritis 9/75 2/18·2 4/40
 Psoriatic arthritis 1/8·3 6/54·5 5/50
 Ankylosing spondylitis 2/16·7 3/27·3 1/10
BCG-vaccinated (n/%) 0 0 0
Risk factors for LTBI (n/%)
 Birth in a TB-endemic area 1/8·3 0 1/10
 History of household contact 0 1/9·1 0
 Chest X-ray suggestive of LTBI 4/33·3 0 0
 Previous diagnosis of TB 0 0 0
Concomitant treatment regimen (n/%)
 Glucocorticoids 0 0 0
 DMARDs 0 0 0
 Biologicals 3/25 8/72·7 4/40
 DMARDs + glucocorticoids 3/25 0 0
 Biologicals + glucocorticoids 1/8·3 1/9·1 1/10
 Biologicals + DMARDs 2/16·7 1/9·1 3/30
 Biologicals + DMARDs + glucocorticoids 1/8·3 0 2/20
 No immunosuppressants 2/16·7 1/9·1 0

Includes Albania (group A) and Argentina (group C). Group A: patients with latent tuberculosis infection (LTBI) (before the onset of biological therapy) showing fluctuations (conversions/reversions) in released interferon (IFN)-γ levels in the QuantiFERON-TB Gold In-Tube (QFT-GIT) during long-term treatment with biological agents. Group B: patients with no evidence of LTBI at baseline showing IFN-γ levels fluctuations during follow-up. Group C: patients with no evidence of LTBI at baseline showing persistently negative IFN-γ levels released in the QFT-GIT during follow-up. BCG = bacille Calmette-Guérin; DMARDs = disease modifying anti-rheumatic drugs; TB = tuberculosis; M/F = male/female. DMARDs include methotrexate, leflunomide, cyclosporin A, sulphasalazine, azathioprine and hydroxychloroquine.