Simvastatin increases the in vivo activity of the first-line tuberculosis regimen
Author(s) -
Ciaran Skerry,
Michael L. Pinn,
Natalie Bruiners,
Richard Pine,
Maria Laura Gennaro,
Petros C. Karakousis
Publication year - 2014
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dku166
Subject(s) - simvastatin , isoniazid , medicine , pharmacology , rifampicin , regimen , tuberculosis , pyrazinamide , in vivo , dosing , rifapentine , mycobacterium tuberculosis , biology , latent tuberculosis , microbiology and biotechnology , pathology
The need to develop new, improved treatments for tuberculosis (TB) remains urgent, and the repurposing of existing drugs represents a possible shortcut to market. Recently, there has been significant interest in host-directed adjuvant therapy to enhance bacillary killing. HMG-CoA reductase inhibitors (statins), which are among the most commonly prescribed drugs, have immunomodulatory properties and improve the clinical outcomes of bacterial infections.
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