Abstract

BackgroundThe reactivation rate of tuberculosis in patients with chronic inflammatory arthritis (CIA) on TNFα inhibitors (TNFi) and baseline negative screening for latent tuberculosis infection (LTBI) is higher than in the general population.AimTo compare the performance of tuberculin skin test (TST), TST-Booster, ELISPOT (T-SPOT.TB) and QuantiFERON-TB Gold in tube (QFT-IT) to detect LTBI in patients with CIA on TNFi.Patients and methodsA total of 102 patients with CIA [rheumatoid arthritis (RA), n = 40; ankylosing spondylitis (AS), n = 35; psoriatic arthritis (PsA), n = 7; and juvenile idiopathic arthritis (JIA), n = 20] were prospectively followed-up for 24 months to identify incident LTBI cases. Epidemiologic data, TST, T-SPOT.TB, QFT-IT and a chest X-ray were performed at baseline and after 6 months of LTBI treatment.ResultsThirty six percent (37/102) of patients had positive TST or Interferon Gamma Release Assays (IGRAs) tests. Agreement among TST and IGRAs was moderate (k = 0.475; p = 0.001), but high between T-SPOT.TB and QFT-IT (k = 0.785; p < 0.001). During the 24-Month follow-up, 15 (18.5%) incident cases of LTBI were identified. In comparison to TST, the IGRAs increased the LTBI diagnosis power in 8.5% (95% CI 3.16–17.49). TST-Booster did not add any value in patients with negative TST at baseline. After 6-Month isoniazid therapy, IGRAs results did not change significantly.ConclusionsAlmost 20% of CIA patients had some evidence of LTBI, suggesting higher conversion rate after exposition to TNFi. TST was effective in identifying new cases of LTBI, but IGRAs added diagnostic power in this scenario. Our findings did not support the repetition of IGRAs after 6-Month isoniazid therapy and this approach was effective to mitigate active TB in 2 years of follow-up.

Highlights

  • TNFα inhibitors are important therapeutic agents used for the management of pain, inflammation, quality of life and function in patients with chronic inflammatory arthritis (CIA), including rheumatoid arthritis (RA) [1], psoriatic arthritis (PsA) [2], ankylosing spondylitis (AS) [3] and juvenile idiopathic arthritis (JIA) [4]

  • In comparison to TST, the Interferon Gamma Release Assays (IGRAs) increased the latent tuberculosis infection (LTBI) diagnosis power in 8.5%

  • Almost 20% of CIA patients had some evidence of LTBI, suggesting higher conversion rate after exposi‐ tion to TNFα inhibitors (TNFi)

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Summary

Introduction

TNFα inhibitors are important therapeutic agents used for the management of pain, inflammation, quality of life and function in patients with chronic inflammatory arthritis (CIA), including rheumatoid arthritis (RA) [1], psoriatic arthritis (PsA) [2], ankylosing spondylitis (AS) [3] and juvenile idiopathic arthritis (JIA) [4]. Gomes et al Advances in Rheumatology (2021) 61:71 these drugs, the monoclonal inhibitors, are associated with an increased risk of reactivation of latent tuberculosis infection (LTBI) [5]. In this context, the clinical presentation of active tuberculosis (TB) occurs in the first 12 months of treatment with biolological drugs and some TB cases are severe, including extrapulmonary and miliary forms, which limit the clinical management of the underlying disease [6]. The reactivation rate of tuberculosis in patients with chronic inflammatory arthritis (CIA) on TNFα inhibitors (TNFi) and baseline negative screening for latent tuberculosis infection (LTBI) is higher than in the general population

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