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Clarithromycin Significantly Improves Interleukin‐12‐Mediated Anti‐Mycobacterium aviumActivity and Abolishes Toxicity in Mice
Author(s) -
Luiz E. Bermudez,
Mary Petrofsky,
Martin Wu,
Lowell S. Young
Publication year - 1998
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/515351
Subject(s) - clarithromycin , toxicity , mycobacterium avium intracellulare infection , medicine , spleen , antibacterial agent , pharmacology , interleukin , mycobacterium , interleukin 2 , regimen , immunology , microbiology and biotechnology , biology , cytokine , antibiotics , pathology , tuberculosis
Treatment of experimental murine Mycobacterium avium (MAC) infection with interleukin-12 (IL-12) significantly decreased MAC organisms in tissue but resulted in toxicity. Because IL-12-related toxicity was seen only in infected mice, IL-12 was combined with clarithromycin in an attempt to decrease bacterial burden. Clarithromycin (200 mg/kg/day) was administered alone to M. avium-infected mice for 1 week, and from week 2, IL-12 (20 microg/kg twice per week) was added to the regimen for 4 weeks. Treatment with IL-12 resulted in 60% mortality, compared with 40% mortality in untreated control mice and 20% when IL-12 was given with clarithromycin (P < .05). Clarithromycin plus IL-12 resulted in increased activity compared with either clarithromycin or IL-12 alone in reducing the number of bacteria in spleen and blood. Although potentially toxic, IL-12 is an effective immunotherapy for MAC infection, and combination with clarithromycin reduces IL-12 toxicity.

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