Markers of gut dysfunction do not explain low rifampicin bioavailability in HIV-associated TB
Author(s) -
Christopher Vinnard,
Shruthi Ravimohan,
Neo Tamuhla,
Jotam G. Pasipanodya,
Shashikant Srivastava,
Chawangwa Modongo,
Nicola M. Zetola,
Drew Weissman,
Tawanda Gumbo,
Gregory P. Bisson
Publication year - 2017
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/dkx111
Subject(s) - bioavailability , rifampicin , human immunodeficiency virus (hiv) , medicine , tuberculosis , antibacterial agent , antibiotics , microbiology and biotechnology , virology , pharmacology , biology , pathology
Rifampicin is the key drug responsible for sterilizing activities in the first-line TB treatment regimen. Damage to the gut during acute and chronic HIV infection may inhibit drug absorptive capacity. We sought to test the hypothesis that markers of intestinal damage, bacterial translocation and systemic immune activation would relate to rifampicin bioavailability among HIV/TB patients.
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