Evolving models of the immunopathogenesis of T cell–mediated drug allergy: The role of host, pathogens, and drug response

KD White, WH Chung, SI Hung, S Mallal… - Journal of Allergy and …, 2015 - Elsevier
Immune-mediated (IM) adverse drug reactions (ADRs) are an underrecognized source of
preventable morbidity, mortality, and cost. Increasingly, genetic variation in the HLA loci is …

Antiretroviral therapy and management of HIV infection

PA Volberding, SG Deeks - The Lancet, 2010 - thelancet.com
Antiretroviral therapy of HIV infection has changed a uniformly fatal into a potentially chronic
disease. There are now 17 drugs in common use for HIV treatment. Patients who can access …

Mortality and causes of death in people diagnosed with HIV in the era of highly active antiretroviral therapy compared with the general population: an analysis of a …

S Croxford, A Kitching, S Desai, M Kall… - The Lancet Public …, 2017 - thelancet.com
Background Deaths in HIV-positive people have decreased since the introduction of highly
active antiretroviral therapy (HAART) in 1996. Fewer AIDS-related deaths and an ageing …

Once-daily dolutegravir versus darunavir plus ritonavir in antiretroviral-naive adults with HIV-1 infection (FLAMINGO): 48 week results from the randomised open-label …

B Clotet, J Feinberg, J van Lunzen, MA Khuong-Josses… - The Lancet, 2014 - thelancet.com
Background Dolutegravir has been shown to be non-inferior to an integrase inhibitor and
superior to a non-nucleoside reverse transcriptase inhibitor (NNRTI). In FLAMINGO, we …

Once-daily dolutegravir versus raltegravir in antiretroviral-naive adults with HIV-1 infection: 48 week results from the randomised, double-blind, non-inferiority SPRING …

F Raffi, A Rachlis, HJ Stellbrink, WD Hardy, C Torti… - The Lancet, 2013 - thelancet.com
Summary Background Dolutegravir (S/GSK1349572) is a once-daily HIV integrase inhibitor
with potent antiviral activity and a favourable safety profile. We compared dolutegravir with …

Co-formulated elvitegravir, cobicistat, emtricitabine, and tenofovir versus co-formulated efavirenz, emtricitabine, and tenofovir for initial treatment of HIV-1 infection: a …

PE Sax, E DeJesus, A Mills, A Zolopa, C Cohen… - The Lancet, 2012 - thelancet.com
Background The integrase inhibitor elvitegravir (EVG) has been co-formulated with the
CYP3A4 inhibitor cobicistat (COBI), emtricitabine (FTC), and tenofovir disoproxil fumarate …

Impact of late diagnosis and treatment on life expectancy in people with HIV-1: UK Collaborative HIV Cohort (UK CHIC) Study

M May, M Gompels, V Delpech, K Porter, F Post… - Bmj, 2011 - bmj.com
Objectives To estimate life expectancy for people with HIV undergoing treatment compared
with life expectancy in the general population and to assess the impact on life expectancy of …

Non-nucleoside reverse transcriptase inhibitors (NNRTIs), their discovery, development, and use in the treatment of HIV-1 infection: a review of the last 20 years (1989 …

MP de Béthune - Antiviral research, 2010 - Elsevier
It is almost 20 years since NNRTIs were identified as a new class of antiretroviral drugs for
the treatment of HIV-1 infection. Although they belong to different and diverse chemical …

Rilpivirine versus efavirenz with tenofovir and emtricitabine in treatment-naive adults infected with HIV-1 (ECHO): a phase 3 randomised double-blind active-controlled …

JM Molina, P Cahn, B Grinsztejn, A Lazzarin, A Mills… - The Lancet, 2011 - thelancet.com
Background Efavirenz with tenofovir-disoproxil-fumarate and emtricitabine is a preferred
antiretroviral regimen for treatment-naive patients infected with HIV-1. Rilpivirine, a new non …

Effect of transmitted drug resistance on virological and immunological response to initial combination antiretroviral therapy for HIV (EuroCoord-CHAIN joint project): a …

L Wittkop, HF Günthard, F De Wolf, D Dunn… - The Lancet infectious …, 2011 - thelancet.com
Background The effect of transmitted drug resistance (TDR) on first-line combination
antiretroviral therapy (cART) for HIV-1 needs further study to inform choice of optimum drug …