Chris Stone

ORCID: 0000-0001-6457-2663
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About
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Research Areas
  • HIV Research and Treatment
  • HIV/AIDS drug development and treatment
  • HIV/AIDS Research and Interventions
  • Diabetes Treatment and Management
  • Peptidase Inhibition and Analysis
  • Cardiac Fibrosis and Remodeling
  • Pancreatic function and diabetes
  • Neuropeptides and Animal Physiology
  • Metabolism, Diabetes, and Cancer
  • Inhalation and Respiratory Drug Delivery
  • Cardiovascular Function and Risk Factors
  • Nuclear Receptors and Signaling
  • Adenosine and Purinergic Signaling
  • Pneumocystis jirovecii pneumonia detection and treatment
  • HIV-related health complications and treatments
  • Food Allergy and Anaphylaxis Research
  • Cardiac Ischemia and Reperfusion
  • Cardiac Imaging and Diagnostics
  • Cardiovascular Disease and Adiposity
  • Electrospun Nanofibers in Biomedical Applications
  • Adipose Tissue and Metabolism
  • Tissue Engineering and Regenerative Medicine
  • Hepatitis C virus research

Rhode Island Hospital
2024

Brown University
2024

SPRINT
2024

National Heart Lung and Blood Institute
2024

Sprint (United States)
2024

Age UK
2003-2004

GlaxoSmithKline (United Kingdom)
2003-2004

Wellcome Library
1998-2001

Goethe University Frankfurt
2000

The Gurdon Institute
2000

The safety, pharmacokinetics, and antiretroviral activity of lamivudine alone in combination with zidovudine was studied pregnant women infected human immunodeficiency virus type 1 (HIV-1) their neonates. Women received the drugs orally from week 38 pregnancy to after delivery. Neonate therapy began 12 h delivery continued for week. Both treatment regimens were well-tolerated newborns. Lamivudine pharmacokinetics similar those nonpregnant adults. freely crossed placenta secreted breast milk....

10.1086/314431 article EN The Journal of Infectious Diseases 1998-11-01

Abacavir (1592U89) is a nucleoside inhibitor of human immunodeficiency virus (HIV) type 1 reverse transcriptase (RT). Resistance to abacavir was studied with alone and in combination other analogues cell culture, isolates from zidovudine/lamivudine clinical trials, the first dose-escalating 12-week trial (CNA2001) evaluate potency. vitro selected for mutations at HIV RT codons K65R, L74V, Y115F, M184V. However, combined zidovudine against M184V mutation. therapy vivo resulted large decreases...

10.1086/315317 article EN The Journal of Infectious Diseases 2000-03-01

Objective To assess the antiviral efficacy, safety and adherence in patients switched to an abacavir-containing nucleoside reverse transcriptase inhibitor (NRTI) regimen after long-term HIV-1 RNA suppression with a dual NRTI/protease (PI) combination. Methods In open-label, multicentre study, receiving 2NRTI plus PI for at least 6 months, history of undetectable plasma since initiation therapy < 50 copies/ml screening, were randomly assigned replace abacavir (n = 105) or continue same...

10.1097/00002030-200108170-00009 article EN AIDS 2001-08-01

To examine changes in HIV-1 susceptibility (genotype and phenotype) during an initial abacavir monotherapy phase followed by the addition of zidovudine lamivudine.Sixty infected, antiretroviral therapy-naive subjects were randomized to receive 100, 300 or 600 mg twice daily. Subjects completing 24 weeks therapy meeting a protocol defined switch criterion could open label abacavir/zidovudine/lamivudine.Plasma reverse transcriptase was genotyped at baseline, week 12, last time point on ABC...

10.1097/00002030-200001280-00012 article EN AIDS 2000-01-01

Objective To evaluate HIV-1 reverse transcriptase genotypic and phenotypic indicators of resistance to abacavir (ABC) as predictors ABC antiviral efficacy. Design The study was a retrospective, combined analysis five multicentre trials in which added single agent background antiretroviral therapy experienced adults. Methods Baseline genotype susceptibility were determined the association phenotype with virological response after addition analysed. Results Overall, 68% these...

10.1177/135965350400900102 article EN Antiviral Therapy 2004-01-01

To compare the antiviral activity of abacavir (ABC) with stable background therapy (SBG) and SBG alone in antiretroviral therapy-experienced subjects as demonstrated by proportion plasma HIV-1 RNA < or = 400 copies/ml, CD4 cell count profiles, safety tolerance two regimens over 16 weeks.One-hundred eighty-five infected adults, counts > 100 x 10(6)/l 400-50,000 copies/ml who had received for at least 12 weeks, were randomized to receive ABC (300 mg twice daily) placebo a double blind,...

10.1097/00002030-200005050-00003 article EN AIDS 2000-05-01

The resistance of HIV clinical isolates with or without M184V was analysed in relation to plasma HIV-1-RNA level and time on therapy. number thymidine analogue mutations (TAMs) lower M184V, this independent therapy for T215F/Y, D67N L210W. This suggests a direct effect the reduced selection TAMs. Lamivudine use significantly associated median fold zidovudine stavudine. Treatments lamivudine lamivudine/zidovudine retain significant activity despite [1,2]. Larder et al. [3] showed that delay...

10.1097/00002030-200208160-00017 article EN AIDS 2002-08-01

BACKGROUND: Coronary artery disease is the leading cause of death worldwide. It imposes an enormous symptomatic burden on patients, leaving many with residual despite optimal procedural therapy and up to one-thirds debilitating angina amenable neither procedures, nor current pharmacological options. Semaglutide (SEM), a GLP-1 (glucagon-like peptide 1) agonist originally approved for management diabetes, has garnered substantial attention its capacity attenuate cardiovascular risk. Although...

10.1161/atvbaha.124.321850 article EN Arteriosclerosis Thrombosis and Vascular Biology 2024-12-12

ABSTRACT Mutations selected or deselected during passage of human immunodeficiency virus strain HXB2 resistant variants with tenofovir (TFV), abacavir (ABC), and lamivudine (3TC) differed depending on the drug combination genotype. In wild-type virus, TFV-ABC TFV-3TC K65R (with reduced susceptibility to all three inhibitors) then Y115F. TFV-containing regimens might increase selection, which confers multiple nucleoside reverse transcriptase inhibitor resistance.

10.1128/aac.48.4.1413-1415.2004 article EN Antimicrobial Agents and Chemotherapy 2004-03-26

Abacavir (ABC) selects for four mutations (K65R, L74V, Y115F and M184V) in HIV-1 reverse transcriptase (RT), both vitro during monotherapy vivo. The aim of this analysis was to compare the selection these other nucleoside inhibitor (NRTI)-associated by ABC-containing therapies presence absence concurrent lamivudine (3TC) and/or zidovudine (ZDV) assess effect on phenotypic susceptibility NRTIs.This study a retrospective patterns NRTI-associated selected following virological failure six...

10.1111/j.1468-1293.2004.00243.x article EN HIV Medicine 2004-11-01

To determine HIV-1 reverse transcriptase (RT) and protease (PRO) mutations selected in isolates from antiretroviral therapy (ART)-experienced patients receiving an efavirenz/abacavir/amprenavir salvage regimen.Open-label, single arm of abacavir, 300 mg twice daily, amprenavir, 1200 daily efavirenz, 600 once ART-experienced which 42% were non-nucleoside inhibitor-naive. The virology population examined consisted all who took at least 16 weeks study drugs (n=74). Plasma sequencing was carried...

10.1177/135965350300800205 article EN Antiviral Therapy 2003-02-01

Our novel lab-grown, human 3-D extracellular matrix (ECM) represents a therapeutic approach to prevent pathological remodeling and heart failure in an animal model of attack. This finding may help develop nonsurgical modalities aimed at reducing the global burden cardiovascular disease.

10.1152/ajpheart.00581.2024 article EN AJP Heart and Circulatory Physiology 2024-12-20

Introduction: Interest is increasing in using novel diabetic medications, such as GLP-1 receptor agonists, to manage coronary artery disease. Dipeptidyl peptidase-4 (DPP-4) inhibitors enhance activity through the same pathway agonists; however, DPP-4 have not been fully evaluated setting of ischemic heart We chose study inhibitor linagliptin (LIN) a swine model chronic myocardial ischemia (CMI). Goals: Study effect LIN clinically relevant CMI gain insight into potential therapies for...

10.1161/circ.150.suppl_1.4143581 article EN Circulation 2024-11-12

Introduction: The effect of obesogenic diet on the outcomes coronary artery disease are controversial with some clinical studies suggesting a paradoxical favorable obesity. We seek to better understand effects high-fat chronic myocardial ischemia using swine model and Proteomic Analysis. Methods: Twenty 6-week-old Yorkshire received 5 weeks normal (n=9, ND) or (n=11, HFD) prior placement an ameroid constrictor left circumflex induce ischemia. continued ND HFD for seven after procedure. At...

10.1161/circ.150.suppl_1.4145779 article EN Circulation 2024-11-12

Interest is increasing in using novel diabetic medications, such as glucagon-like peptide 1 (GLP-1) receptor agonists, to manage coronary artery disease. Dipeptidyl peptidase-4 (DPP-4) inhibitors enhance GLP-1 activity through the same pathway agonists; however, DPP-4 have not been fully evaluated setting of ischemic heart We chose study inhibitor linagliptin (LIN) a porcine model chronic ischemia. Seventeen Yorkshire swine underwent left thoracotomy and ameroid constrictor placement over...

10.1016/j.jpet.2024.100532 article EN Journal of Pharmacology and Experimental Therapeutics 2024-12-24

Objective Although both clinical data and animal models suggest cardiovascular benefits following administration of Dipeptidyl Peptidase 4 (DPP-4) inhibitors, the underlying mechanisms remain unclear. We therefore sought to evaluate effect DPP-4 inhibitor sitagliptin on myocardial fibrosis, insulin signaling in chronic ischemia using a swine model. An ameroid constrictor placement left coronary circumflex artery thirteen Yorkshire model ischemia. After two weeks recovery, were assigned one...

10.1371/journal.pone.0307922 article EN cc-by PLoS ONE 2024-07-29
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