Literature DB >> 18602126

Tackling tissue destruction in tuberculosis.

Jon S Friedland1.   

Abstract

Drug-resistant tuberculosis (TB) is a major worldwide problem. The immune system usually controls TB, but once active disease develops, the inflammatory immune response drives tissue destruction. Tissue damage is a result of enzymatic activity, and matrix metalloproteinases (MMPs) have a key role. There are a few new anti-mycobacterial drugs in trial and some vaccine candidates in development but options for control of TB are limited. A novel approach may be to combine antibiotic therapy with limiting the activity of the key mediators of tissue damage, such as MMPs, by inhibiting either the enzymes directly or the pathways that regulate them.

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Year:  2008        PMID: 18602126     DOI: 10.1016/j.trstmh.2008.05.008

Source DB:  PubMed          Journal:  Trans R Soc Trop Med Hyg        ISSN: 0035-9203            Impact factor:   2.184


  1 in total

1.  Antimycobacterial drugs modulate immunopathogenic matrix metalloproteinases in a cellular model of pulmonary tuberculosis.

Authors:  Shivani Singh; Andre Kubler; Utpal K Singh; Ajay Singh; Harriet Gardiner; Rajniti Prasad; Paul T Elkington; Jon S Friedland
Journal:  Antimicrob Agents Chemother       Date:  2014-06-02       Impact factor: 5.191

  1 in total

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