TY - JOUR
T1 - Early antiretroviral therapy and potent second-line drugs could decrease HIV incidence of drug resistance
AU - Shen, Mingwang
AU - Xiao, Yanni
AU - Rong, Libin
AU - Meyers, Lauren Ancel
AU - Bellan, Steven E.
N1 - Publisher Copyright:
© 2017 The Author(s) Published by the Royal Society. All rights reserved.
PY - 2017/6/28
Y1 - 2017/6/28
N2 - Early initiation of antiretroviral therapy (ART) reduces the risk of drug-sensitive HIV transmission butmay increase the transmission of drug-resistant HIV. We used a mathematical model to estimate the long-term population-level benefits of ART and determine the scenarios under which earlier ART (treatment at 1 year post-infection, on average) could decrease simultaneously both total and drug-resistant HIV incidence (new infections). We constructed an infection-age-structured mathematical model that tracked the transmission rates over the course of infection andmodelled the patients’ life expectancy as a function ofART initiation timing.We fitted this model to the annual AIDS incidence and death data directly, and to resistance data and demographic data indirectly among men who have sex with men (MSM) in San Francisco. Using counterfactual scenarios, we assessed the impact on total and drug-resistant HIV incidence of ART initiation timing, frequency of acquired drug resistance, and second-line drug effectiveness (defined as the combination of resistance monitoring, biomedical drug efficacy and adherence). Earlier ART initiation could decrease the number of both total and drug-resistant HIV incidence when second-line drug effectiveness is sufficiently high (greater than 80%), but increase the proportion of newinfections that are drug resistant. Thus, resistance may paradoxically appear to be increasing while actually decreasing.
AB - Early initiation of antiretroviral therapy (ART) reduces the risk of drug-sensitive HIV transmission butmay increase the transmission of drug-resistant HIV. We used a mathematical model to estimate the long-term population-level benefits of ART and determine the scenarios under which earlier ART (treatment at 1 year post-infection, on average) could decrease simultaneously both total and drug-resistant HIV incidence (new infections). We constructed an infection-age-structured mathematical model that tracked the transmission rates over the course of infection andmodelled the patients’ life expectancy as a function ofART initiation timing.We fitted this model to the annual AIDS incidence and death data directly, and to resistance data and demographic data indirectly among men who have sex with men (MSM) in San Francisco. Using counterfactual scenarios, we assessed the impact on total and drug-resistant HIV incidence of ART initiation timing, frequency of acquired drug resistance, and second-line drug effectiveness (defined as the combination of resistance monitoring, biomedical drug efficacy and adherence). Earlier ART initiation could decrease the number of both total and drug-resistant HIV incidence when second-line drug effectiveness is sufficiently high (greater than 80%), but increase the proportion of newinfections that are drug resistant. Thus, resistance may paradoxically appear to be increasing while actually decreasing.
KW - Acquired drugresistance
KW - Early antiretroviral therapy initiation
KW - Mathematical model
KW - Second-line drug effectiveness
KW - Transmission of drug-resistant HIV
UR - https://www.scopus.com/pages/publications/85021642877
U2 - 10.1098/rspb.2017.0525
DO - 10.1098/rspb.2017.0525
M3 - 文章
C2 - 28659449
AN - SCOPUS:85021642877
SN - 0962-8452
VL - 284
JO - Proceedings of the Royal Society B: Biological Sciences
JF - Proceedings of the Royal Society B: Biological Sciences
IS - 1857
M1 - 20170525
ER -