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Published on: October 5, 2015
Disseminated mycobacterial infections after tumor necrosis factor inhibitor use, revealing inborn errors of immunity
Jacqueline D Squire1, Claudia R Libertin2, Harry Powers2
1Division of Pulmonary, Allergy, and Sleep Medicine, Mayo Clinic, Jacksonville, USA.
Abstract:
Tumor necrosis factor-a inhibitors can be associated with increased risk of infections, particularly reactivation of latent tuberculosis or nontuberculous mycobacterium (NTM). However, because disseminated NTM is rare, inborn errors of immunity should be considered. We present three patients with disseminated NTM after tumor necrosis factor-a inhibitor use who were found to have inborn errors of immunity.
Insights
Tumor necrosis factor-a inhibitors increase infection risk. Disseminated nontuberculous mycobacterium (NTM) in patients using these drugs may indicate underlying inborn errors of immunity.
Area of Science:
- Immunology
- Infectious Diseases
- Genetics
Background:
- Tumor necrosis factor-alpha (TNF-a) inhibitors are widely used for inflammatory conditions.
- TNF-a inhibitors are known to increase the risk of infections, including mycobacterial diseases.
Observation:
- Disseminated nontuberculous mycobacterium (NTM) infections are rare but serious complications.
- Three patients developed disseminated NTM following treatment with TNF-a inhibitors.
Findings:
- Genetic analysis revealed inborn errors of immunity in all three patients with disseminated NTM.
- These genetic conditions likely predisposed the patients to severe NTM infections when immune surveillance was reduced by TNF-a inhibition.
Implications:
- The findings suggest that patients on TNF-a inhibitors who develop disseminated NTM should be evaluated for inborn errors of immunity.
- Early identification of these genetic immune deficiencies can guide appropriate management and prevent further opportunistic infections.
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