TY - JOUR
T1 - Carbapenems against Mycobacterium tuberculosis
T2 - A review of the evidence
AU - Jaganath, D.
AU - Lamichhane, G.
AU - Shah, M.
N1 - Funding Information:
MS is funded by the National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Bethesda, MD, USA, under grant #K23AI089259. GL was supported by the NIH grant #DP2OD008459
Publisher Copyright:
© 2016 The Union.
PY - 2016/11/1
Y1 - 2016/11/1
N2 - Carbapenems, a more recent β-lactam class, represent a unique anti-tuberculosis option, as emerging evidence demonstrates that they target the Mycobacterium tuberculosis cell wall and β-lactamase. This provides a potentially new agent against M. tuberculosis, in particular for multidrug-resistant (MDR) and extensively drug-resistant (XDR) tuberculosis (TB), where options are limited. In this review, we examine the current evidence on the activity of carbapenems against M. tuberculosis. The predominance of work is in vitro, and suggests that carbapenems kill M. tuberculosis at least in the active phase, with possible greater potency with the addition of a β-lactamase inhibitor. The few in vivo and clinical studies suggest that there are benefits and that they are generally tolerated, although the variability in duration, dosing, and background regimen and lack of pharmacokinetic analyses limit interpretation of efficacy. We outline further areas of research to better understand the role of carbapenems to add a needed new agent to the treatment of MDR- and XDRTB.
AB - Carbapenems, a more recent β-lactam class, represent a unique anti-tuberculosis option, as emerging evidence demonstrates that they target the Mycobacterium tuberculosis cell wall and β-lactamase. This provides a potentially new agent against M. tuberculosis, in particular for multidrug-resistant (MDR) and extensively drug-resistant (XDR) tuberculosis (TB), where options are limited. In this review, we examine the current evidence on the activity of carbapenems against M. tuberculosis. The predominance of work is in vitro, and suggests that carbapenems kill M. tuberculosis at least in the active phase, with possible greater potency with the addition of a β-lactamase inhibitor. The few in vivo and clinical studies suggest that there are benefits and that they are generally tolerated, although the variability in duration, dosing, and background regimen and lack of pharmacokinetic analyses limit interpretation of efficacy. We outline further areas of research to better understand the role of carbapenems to add a needed new agent to the treatment of MDR- and XDRTB.
KW - Anti-tuberculosis
KW - Antibiotics
KW - Extensively drug-resistant tuberculosis
KW - Group D
KW - Multidrug-resistant tuberculosis
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U2 - 10.5588/ijtld.16.0498
DO - 10.5588/ijtld.16.0498
M3 - Review article
C2 - 27776583
AN - SCOPUS:84992504914
SN - 1027-3719
VL - 20
SP - 1436
EP - 1447
JO - International Journal of Tuberculosis and Lung Disease
JF - International Journal of Tuberculosis and Lung Disease
IS - 11
ER -