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Dolutegravir Monotherapy of Simian Immunodeficiency Virus-Infected Macaques Selects for Several Patterns of Resistance Mutations with Variable Virological Outcomes
Author(s) -
Koen K. A. Van Rompay,
Said Hassounah,
Brandon F. Keele,
Jeffrey D. Lifson,
Amir Ardeshir,
Jennifer Watanabe,
Hanh Thi Pham,
Elena Chertova,
Raymond C. Sowder,
Jan Balzarini,
Thibault Mésplède,
Mark A. Wainberg
Publication year - 2018
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.01189-18
Subject(s) - dolutegravir , virology , biology , drug resistance , simian immunodeficiency virus , virus , viral replication , drug , viral load , antiviral drug , human immunodeficiency virus (hiv) , lentivirus , immunology , viral disease , pharmacology , genetics , antiretroviral therapy
A growing number of anti-HIV drug combinations are effective in suppressing virus replication in HIV-infected persons. However, to reduce their cost and risk for toxicity, there is considerable interest in simplifying drug regimens. A major concern with single-drug regimens is the emergence of drug-resistant viral mutants. It has been speculated that DTG monotherapy may be a feasible option, because DTG may have a higher genetic barrier for the development of drug resistance than other commonly used antiretrovirals. To explore treatment initiation with DTG monotherapy, we started SIV-infected macaques on DTG during either acute or chronic infection. Although DTG initially reduced virus replication, continued treatment led to the emergence of a variety of viral mutations previously described to confer low-level resistance of HIV-1 to DTG, and this was associated with variable clinical outcomes. This unpredictability of mutational pathways and outcomes warns against using DTG monotherapy as initial treatment for HIV-infected people.

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