In Vitro Activity of Human Immunodeficiency Virus Protease Inhibitors againstPneumocystis carinii
Author(s) -
Chiara Atzori,
Elena Angeli,
Annalisa Mainini,
F Agostoni,
Valeria Micheli,
Antonietta Cargnel
Publication year - 2000
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/315437
Subject(s) - saquinavir , nelfinavir , indinavir , pneumocystis carinii , ritonavir , protease , virology , protease inhibitor (pharmacology) , pneumocystis pneumonia , biology , pneumonia , immunology , proteases , microbiology and biotechnology , medicine , pneumocystis jirovecii , virus , human immunodeficiency virus (hiv) , viral disease , sida , viral load , antiretroviral therapy , enzyme , biochemistry
Since 1996, the introduction of protease inhibitors (PIs) has led to a dramatic decrease of human immunodeficiency virus-related Pneumocystis carinii pneumonia. This effect is clearly due, in large part, to the induction of immune reconstitution by highly active antiretroviral therapy (HAART). However, it is conceivable that PIs had other beneficial effects, including direct activity against Pneumocystis. In this study, the occurrence of specific aspartyl proteases in Pneumocystis is described. These protease targets seemed to be affected in vitro by antiretroviral PIs. These data suggest intriguing implications for the possible antipneumocystis benefit of receiving indinavir, ritonavir, nelfinavir, or saquinavir during HAART.
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