Challenges in Diagnosing Latent Tuberculosis Infection in Patients Treated with Tumor Necrosis Factor Antagonists

被引:38
作者
Keystone, Edward C. [1 ]
Papp, Kim A. [2 ]
Wobeser, Wendy [3 ]
机构
[1] Mt Sinai Hosp, Rebecca MacDonald Ctr Arthrit & Autoimmune Dis, Toronto, ON M5T 3L9, Canada
[2] Prob Med Res, Waterloo, ON, Canada
[3] Queens Univ, Dept Med, Div Infect Dis, Kingston, ON K7L 3N6, Canada
关键词
TUMOR NECROSIS FACTOR-alpha; LATENT TUBERCULOSIS INFECTION; ANERGY; TUBERCULIN TEST; INTERFERON-gamma; DELAYED HYPERSENSITIVITY; DELAYED-TYPE HYPERSENSITIVITY; INTERFERON-GAMMA ASSAY; QUANTIFERON-TB GOLD; RHEUMATOID-ARTHRITIS; MYCOBACTERIUM-TUBERCULOSIS; SKIN-TEST; IN-VITRO; TRANSPLANT RECIPIENTS; ANTIRHEUMATIC DRUGS; HIGH PREVALENCE;
D O I
10.3899/jrheum.100623
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Reactivation of latent tuberculosis infection (LTBI) is well recognized as an adverse event associated with anti-tumor necrosis factor-alpha (anti-TNF-alpha) therapy. The strengths and weaknesses of current techniques for detecting LTBI in patients with chronic inflammatory diseases such as rheumatoid arthritis (RA) and psoriasis have not been fully examined. T cell hyporesponsiveness due to immunosuppression caused by illness or drugs, referred to as anergy, may produce false-negative tuberculin skin test (TST) and interferon-gamma release assay (IGRA) results. The literature suggests that anergy may influence screening performance of TST and IGRA tests in candidates for anti-TNF-alpha therapy. Conversely, the potential for false-positive TST and IGRA results must be considered, as treatment for LTBI may be associated with significant morbidity. This review examines the reliability issues related to LTBI diagnostic testing and provides practical direction to help prevent LTBI reactivation and facilitate successful anti-TNF-alpha treatment. (First Release April 1 2011; J Rheumatol 2011;38:1234-43; doi:10.3899/jrheum.100623)
引用
收藏
页码:1234 / 1243
页数:10
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