Protease inhibitors: a therapeutic breakthrough for the treatment of patients with human immunodeficiency virus

As one of the largest growing classes of antiretroviral drugs, protease inhibitors are promising agents for the management of patients infected with the human immuno deficiency virus (HIV). We reviewed the literature and compared efficacy, dosing, side effects, and drug-interaction profiles of the p...

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Published inClinical therapeutics Vol. 19; no. 2; pp. 187 - 214
Main Authors Lewis, James S., Terriff, Colleen M., Coulston, Daniel R., Garrison, Mark W.
Format Journal Article
LanguageEnglish
Published Belle Mead, NJ EM Inc USA 01.03.1997
Excerpta Medica
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Abstract As one of the largest growing classes of antiretroviral drugs, protease inhibitors are promising agents for the management of patients infected with the human immuno deficiency virus (HIV). We reviewed the literature and compared efficacy, dosing, side effects, and drug-interaction profiles of the protease inhibitors saquinavir, ritonavir, indinavir, and nelfinavir. We addressed the used of these antiprotease agents as monotherapy versus use in combination therapy with other antiretroviral medications, and the potential for HIV to develop resistance to this drug class. We also discussed therapy with dual protease inhibitors and the use of protease inhibitors in pregnant or lactating women and in pediatric patients. Finally, we examined case reports of the addition of protease inhibitors to an antiretroviral regimen that ultimately decreases or reverses opportunistic infections
AbstractList As one of the largest growing classes of antiretroviral drugs, protease inhibitors are promising agents for the management of patients infected with the human immunodeficiency virus (HIV). We reviewed the literature and compared efficacy, dosing, side effects, and drug-interaction profiles of the protease inhibitors saquinavir, ritonavir, indinavir, and nelfinavir. We addressed the use of these antiprotease agents as monotherapy versus use in combination therapy with other antiretroviral medications, and the potential for HIV to develop resistance to this drug class. We also discussed therapy with dual protease inhibitors and the use of protease inhibitors in pregnant or lactating women and in pediatric patients. Finally, we examined case reports of the addition of protease inhibitors to an antiretroviral regimen that ultimately decreases or reverses opportunistic infections.
As one of the largest growing classes of antiretroviral drugs, protease inhibitors are promising agents for the management of patients infected with the human immuno deficiency virus (HIV). We reviewed the literature and compared efficacy, dosing, side effects, and drug-interaction profiles of the protease inhibitors saquinavir, ritonavir, indinavir, and nelfinavir. We addressed the used of these antiprotease agents as monotherapy versus use in combination therapy with other antiretroviral medications, and the potential for HIV to develop resistance to this drug class. We also discussed therapy with dual protease inhibitors and the use of protease inhibitors in pregnant or lactating women and in pediatric patients. Finally, we examined case reports of the addition of protease inhibitors to an antiretroviral regimen that ultimately decreases or reverses opportunistic infections
Author Lewis, James S.
Terriff, Colleen M.
Coulston, Daniel R.
Garrison, Mark W.
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Issue 2
Keywords human immunodeficiency virus
protease inhibitors
indinavir
nelfinavir
saquinavir
ritonavir
Human
Immunopathology
Monograph
Enzyme
Enzyme inhibitor
AIDS
Review
Immune deficiency
Infection
Peptidases
Chemotherapy
Treatment
Viral disease
Hydrolases
Antiviral
Language English
License CC BY 4.0
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PublicationTitle Clinical therapeutics
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Excerpta Medica
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  article-title: Evaluation of the pharmacokinetic interaction between ritonavir and delavirdine in healthy volunteers
  publication-title: Program and Abstracts of the Fourth Conference on Retroviruses and Opportunistic Infections
  contributor:
    fullname: Ferry
– year: 15181996
  ident: 10.1016/S0149-2918(97)80110-5_BIB51
  article-title: Absence of interaction between indinavir and fluconazole: A pharmacokinetic study in HIV patients
  publication-title: Program and Abstracts of the 36th Interscience Conference on Antimicrobial Agents and Chemotherapy, American Society for Microbiology
  contributor:
    fullname: De Wit
– volume: 8
  start-page: 1065
  year: 1992
  ident: 10.1016/S0149-2918(97)80110-5_BIB60
  article-title: HIV drug resistance
  publication-title: AIDS Res Hum Retroviruses
  doi: 10.1089/aid.1992.8.1065
  contributor:
    fullname: Richman
– year: 22261997
  ident: 10.1016/S0149-2918(97)80110-5_BIB49
  article-title: Effect of nevirapine on pharmacokinetics of indinavir and ritonavir in HIV-1 patients
  publication-title: Program and Abstracts of the Fourth Conference on Retroviruses and Opportunistic Infections
  contributor:
    fullname: Murphy
– year: 22261997
  ident: 10.1016/S0149-2918(97)80110-5_BIB77
  article-title: Salvage therapy using the combination of ritonavir and saquinavir in patients with advanced HIV infection
  publication-title: Program and Abstracts of the Fourth Conference on Retroviruses and Opportunistic Infections
  contributor:
    fullname: Steinhart
– volume: 2
  year: 1996
  ident: 10.1016/S0149-2918(97)80110-5_BIB10
  article-title: How the protease inhibitors work: Their mechanism of action, with schematic color illustrations
  publication-title: HIV Newsline
– year: 7121996
  ident: 10.1016/S0149-2918(97)80110-5_BIB21
  article-title: Assessment of single- and multiple-dose interactions between ritonavir and saquinavir
  publication-title: Program and Abstracts of the XI International Conference on AIDS
  contributor:
    fullname: Hsu
– year: 15181996
  ident: 10.1016/S0149-2918(97)80110-5_BIB24
  article-title: Rifabutin reduces saquinavir plasma levels in HIV-infected patients
  publication-title: Program and Abstracts of the 36th Interscience Conference on Antimicrobial Agents and Chemotherapy, American Society for Microbiology
  contributor:
    fullname: Sahai
– year: 22261997
  ident: 10.1016/S0149-2918(97)80110-5_BIB47
  article-title: Investigations of nelfinavir mesylate pharmacokinetic interactions with indinavir and ritonavir
  publication-title: Program and Abstracts of the Fourth Conference on Retroviruses and Opportunistic Infections
  contributor:
    fullname: Yuen
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Snippet As one of the largest growing classes of antiretroviral drugs, protease inhibitors are promising agents for the management of patients infected with the human...
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elsevier
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SubjectTerms AIDS-Related Opportunistic Infections - drug therapy
Animals
Antibiotics. Antiinfectious agents. Antiparasitic agents
Antiviral agents
Biological and medical sciences
Drug Interactions
Drug Therapy, Combination
Female
HIV Infections - drug therapy
human immunodeficiency virus
Humans
indinavir
Lactation - drug effects
Medical sciences
nelfinavir
Pharmacology. Drug treatments
Pregnancy
protease inhibitors
Protease Inhibitors - adverse effects
Protease Inhibitors - pharmacology
Protease Inhibitors - therapeutic use
ritonavir
saquinavir
Title Protease inhibitors: a therapeutic breakthrough for the treatment of patients with human immunodeficiency virus
URI https://dx.doi.org/10.1016/S0149-2918(97)80110-5
https://www.ncbi.nlm.nih.gov/pubmed/9152561
Volume 19
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