Lower incidence of HIV-1 blips observed during integrase inhibitor-based combination antiretroviral therapy

2021 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Suzan Dijkstra ◽  
L. Marije Hofstra ◽  
Tania Mudrikova ◽  
Annemarie M.J. Wensing ◽  
Patrick G.A. Oomen ◽  
...  
2010 ◽  
Vol 51 (5) ◽  
pp. 620-628 ◽  
Author(s):  
Viktor von Wyl ◽  
Maryam Ehteshami ◽  
Lisa M. Demeter ◽  
Philippe Bürgisser ◽  
Monique Nijhuis ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Anna Prats ◽  
Ignacio Martínez-Zalacaín ◽  
Beatriz Mothe ◽  
Eugènia Negredo ◽  
Núria Pérez-Álvarez ◽  
...  

AbstractIntegrase strand transfer inhibitors (INSTI) are a main component of the current antiretroviral regimens recommended for treatment of HIV infection. However, little is known about the impact of INSTI on neurocognition and neuroimaging. We developed a prospective observational trial to evaluate the effects of INSTI-based antiretroviral therapy on comprehensive brain outcomes (cognitive, functional, and imaging) according to the time since HIV-1 acquisition. We recruited men living with HIV who initiated antiretroviral therapy with INSTI < 3 months since the estimated date of HIV-1 acquisition (n = 12) and > 6 months since estimated date of HIV-1 acquisition (n = 15). We also recruited a group of matched seronegative individuals (n = 15). Assessments were performed at baseline (before initiation of therapy in HIV arms) and at weeks 4 and 48. Baseline cognitive functioning was comparable between the arms. At week 48, we did not find cognitive differences between starting therapy with INSTI earlier than 3 months or later than 6 months after acquisition of HIV-1 infection. Functional status was poorer in individuals diagnosed earlier. This effect recovered 48 weeks after initiation of therapy. Regarding brain imaging, we found that men living with HIV initiating antiretroviral therapy later experienced a greater decrease in medial orbitofrontal cortex over time, with expected negative repercussions for decision-making tasks.


Author(s):  
Sonia Napravnik ◽  
David Edwards ◽  
Paul Stewart ◽  
Brant Stalzer ◽  
Elizabeth Matteson ◽  
...  

2020 ◽  
Vol Volume 13 ◽  
pp. 4389-4394
Author(s):  
Yun Lan ◽  
Linghua Li ◽  
Weilie Chen ◽  
Xizi Deng ◽  
Junbin Li ◽  
...  

2019 ◽  
Vol 63 (5) ◽  
Author(s):  
Robert A. Smith ◽  
Dana N. Raugi ◽  
Vincent H. Wu ◽  
Christopher G. Zavala ◽  
Jennifer Song ◽  
...  

ABSTRACTWe compared the activity of the integrase inhibitor bictegravir against HIV-1 and HIV-2 using a culture-based, single-cycle assay. Values of 50% effective concentrations ranged from 1.2 to 2.5 nM for 9 HIV-1 isolates and 1.4 to 5.6 nM for 15 HIV-2 isolates. HIV-2 integrase mutants G140S/Q148R and G140S/Q148H were 34- and 110-fold resistant to bictegravir, respectively; other resistance-associated mutations conferred ≤5-fold changes in bictegravir susceptibility. Our findings indicate that bictegravir-based antiretroviral therapy should be evaluated in HIV-2-infected individuals.


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