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Journal of Clinical Microbiology, September 1999, p. 2910-2912, Vol. 37, No. 9
Departments of
Virology1 and Infectious
Diseases,2 Pitié-Salpêtrière
Hospital, Paris, France
Received 4 January 1999/Returned for modification 19 April
1999/Accepted 14 June 1999
In order to analyze the impact of protease gene polymorphism on
response to regimens containing a protease inhibitor, the entire
protease coding domain from 58 human immunodeficiency virus type 1 (HIV-1)-infected patients who were protease inhibitor naive was
sequenced before therapy was started. Plasma HIV-1 RNA levels were
measured at baseline and at month 3 and month 6 after treatment. All
patients were treated with a combination of two reverse transcriptase inhibitors and a protease inhibitor (saquinavir EOF
[n = 28], ritonavir [n = 16], or
indinavir [n = 14]). Before treatment, 30 different
positions whose codons differed from the subtype B consensus sequence
were observed. Major mutations associated with protease inhibitor
resistance were not observed. No statistical correlation between the
number of amino acid differences and the treatment efficacy at month 3 (
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Polymorphism of the Human Immunodeficiency Virus
Type 1 (HIV-1) Protease Gene and Response of HIV-1-Infected Patients to
a Protease Inhibitor
2.4 log) or month 6 (
2.7 log) was observed. At baseline, genotypic
analysis of the HIV-1 protease gene of patients who have never received
a protease inhibitor does not allow prediction of the efficacy of
regimens containing a protease inhibitor.
*
Corresponding author. Mailing address: Department of
Virology
CERVI, Hôpital Pitié-Salpêtrière,
47-83 Bd de l'Hôpital, 75651 Paris Cedex 13, France. Phone: 33 1 42 17 74 09. Fax: 33 1 42 17 74 11. E-mail:
vincent.calvez{at}psl.ap-hop-paris.fr.
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