Effect of protease inhibitor-containing regimens on lymphocyte multidrug resistance transporter expression
Author(s) -
Jennifer Lynn Ford
Publication year - 2003
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/dkg381
Subject(s) - indinavir , nelfinavir , saquinavir , ritonavir , lopinavir , amprenavir , pharmacology , p glycoprotein , biology , protease inhibitor (pharmacology) , peripheral blood mononuclear cell , stavudine , microbiology and biotechnology , virology , protease , multiple drug resistance , viral load , in vitro , zidovudine , hiv 1 protease , drug resistance , virus , biochemistry , viral disease , antiretroviral therapy , enzyme
Increased expression of multidrug resistance transporters, such as P-glycoprotein (P-gp), has been suggested as a potential mechanism for decreased protease inhibitor (PI) availability at certain intracellular sites and tissue compartments.
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