TNF-alpha antagonist therapy modify the tuberculin skin test response View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2011-09

AUTHORS

Tulin Cagatay, Zeki Kilicaslan, Penbe Cagatay, Munevver Mertsoylu, Ziya Gulbaran, Reyhan Yildiz, Leyla Pur, Sevil Kamali, Ahmet Gul

ABSTRACT

Tumour necrosis factor-alpha (TNF-α) antagonist drugs have been associated with increased risk of tuberculosis (TB). Tuberculin skin test (TST) is the most frequently used tool for identification of latent TB infection. We herein aimed to analyse the effect of TNF-α antagonists on the TST responses in a prospective study. The study group consisted of 182 patients (99 female, 83 male) who received TNF-α antagonists for various rheumatic disorders. All patients were evaluated with TST along with other parameters on the day of referral and on the 12th month visit. For those patients with a response of <5 mm induration at the initial evaluation, the TST was repeated to observe the booster effect. Out of 182 patients, 87 patients (48%) had a negative (0-4 mm) and 95 (52%) had a positive (≥ 5 mm) TST response at initial evaluation. The TST responses were converted from negative at initial visit to positive at 1-year repeat in 26 (30%) patients. A significant increase was observed in the diameters of TST that were repeated on the first year of TNF-α antagonist treatment (9.15 ± 0.55) compared to their initial diameters (6.60 ± 0.51) (P < 0.001). Increased TST responses in patients receiving TNF-α antagonists may be associated with the restoration of suppressed immune reactivity against TB antigens with the decreased disease activity. The meaning of TST conversion in the definition of latent TB infection and the need for chemoprophylaxis in these patients remains to be answered by further studies. More... »

PAGES

1147-1151

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00296-010-1424-3

DOI

http://dx.doi.org/10.1007/s00296-010-1424-3

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1040244806

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/20349071


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