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Resistance Profiles in Patients with Viral Rebound on Potent Antiretroviral Therapy
Author(s) -
Alessandro CozziLepri,
Caroline Sabin,
Schlomo Staszewski,
Kurt Hertogs,
Axel H. E. Müller,
Holger F. Rabenau,
Andrew Phillips,
Veronica Miller
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 - 10.1086/315301
Subject(s) - nevirapine , lamivudine , zidovudine , regimen , viral load , drug resistance , virology , protease inhibitor (pharmacology) , medicine , reverse transcriptase inhibitor , reverse transcriptase , viral disease , virus , biology , antiretroviral therapy , polymerase chain reaction , microbiology and biotechnology , hepatitis b virus , biochemistry , gene
The prevalence of phenotypic drug resistance was assessed in 60 patients with a viral rebound after they received a protease inhibitor (PI)- or nonnucleoside reverse transcriptase inhibitor (NNRTI)-containing regimen (baseline). Resistance testing was done within 36 weeks of viral rebound; no resistance testing was available at baseline. All patients had previously received zidovudine; 86.0% had received lamivudine. In total, 45.1% of the patients had strains resistant to the PI that they started and 88.9% given nevirapine had strains with reduced susceptibility to that drug. Overall, 46 patients (76.7%) harbored a strain resistant to >/=1 drug of their initial PI- or NNRTI-containing regimen. Of 53 patients who remained on treatment at the time of the study (40 had switched to a different combination from that at baseline), 6 harbored isolates susceptible to all drugs they had ever received. Thus, patients with viral rebound while on potent antiretroviral therapy usually have reduced susceptibility to >/=1 drug. Viral rebound also occurs in persons in whom resistant strains could not be detected by the assay used.

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