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Infections Associated with Tumor Necrosis Factor‐α Antagonists
Author(s) -
Rychly David J.,
DiPiro Joseph T.
Publication year - 2005
Publication title -
pharmacotherapy: the journal of human pharmacology and drug therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.227
H-Index - 109
eISSN - 1875-9114
pISSN - 0277-0008
DOI - 10.1592/phco.2005.25.9.1181
Subject(s) - medicine , tuberculosis , adalimumab , etanercept , infliximab , immunology , tumor necrosis factor alpha , mycobacterium tuberculosis , rifabutin , proinflammatory cytokine , pathology , inflammation , clarithromycin , helicobacter pylori
Tumor necrosis factor‐α (TNF‐α) is a proinflammatory cytokine involved in a wide range of important physiologic processes. This cytokine has a pathologic role in some diseases, and TNF‐α antagonists are effective in treating inflammatory conditions. Given the putative role of TNF‐α in host defense against tuberculosis and other infections, the risk of infection with TNF‐α antagonists is a concern. Therefore, we searched the literature for reports of tuberculosis and other infections associated with TNF‐α–antagonist therapy. Although tuberculosis was rarely reported in randomized clinical comparisons of these antagonists, case reports and submissions to the MedWatch program of the United States Food and Drug Administration have been numerous. Most instances were associated with infliximab, but etanercept and adalimumab may also be associated with an increased risk of tuberculosis. Histoplasmosis, listeriosis, aspergillosis, coccidioidomycosis, and candidiasis have been associated with TNF‐α antagonists, but the causative relationship is not clear. Potential recipients of these drugs should be rigorously screened with skin testing, detailed questioning about recent travel and potential tuberculosis exposure, assessment for symptoms such as cough and weight loss, and chest radiography to minimize their risk of acquiring or reactivating tuberculosis. As with other immunosuppressant drugs, TNF‐α antagonists should not be given to patients with active infection.

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