z-logo
open-access-imgOpen Access
Developing New Drugs for Mycobacterium tuberculosis Therapy: What Information Do We Get from Preclinical Animal Models?
Author(s) -
George L. Drusano,
Brandon Duncanson,
Charles A. Scanga,
Sarah Kim,
Stephan Schmidt,
Michael Neely,
Walter M. Yamada,
Michael Vicchiarelli,
Charles A. Peloquin,
Arnold Louie
Publication year - 2020
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.01376-20
Subject(s) - mycobacterium tuberculosis , linezolid , pharmacokinetics , tuberculosis , animal model , medicine , animal studies , pharmacology , biology , immunology , bacteria , pathology , vancomycin , staphylococcus aureus , genetics
Preclinical animal models of infection are employed to develop new agents but also to screen among molecules to rank them. There are often major differences between human pharmacokinetic (PK) profiles and those developed by animal models of infection, and these may lead to substantial differences in efficacy relative to that seen in humans. Linezolid is a repurposed agent employed to great effect for therapy ofMycobacterium tuberculosis . In this study, we used the hollow-fiber infection model (HFIM) to evaluate the impact of different pharmacokinetic profiles of mice and nonhuman primates (NHP) versus humans on bacterial cell kill as well as resistance suppression.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom