TY - JOUR
T1 - Patterns of resistance mutations selected by treatment of human immunodeficiency virus type 1 infection with zidovudine, didanosine, and nevirapine
AU - Hanna, George J.
AU - Johnson, Victoria A.
AU - Kuritzkes, Daniel R.
AU - Richman, Douglas D.
AU - Leigh Brown, Andrew J.
AU - Savara, Anu V.
AU - Hazelwood, J. Darren
AU - D'Aquila, Richard T.
N1 - Funding Information:
Financial support: NIH (grants AI29193, AI07387, AI01696, AI27659, AI40876, AI32775, AI27767, AI32770, AI27670, AI38858, AI36214, and AI29164; contract 96VC001); Core Laboratory Research Facilities of the University of Alabama at Birmingham School of Medicine; University of Alabama at Birmingham Center for AIDS Research; Birmingham Veterans Affairs Medical Center; and Research Center for AIDS and HIV Infection of the San Diego Veterans Affairs Medical Center. Supplemental support for virology studies was provided by Boehringer Ingelheim Pharmaceuticals, Inc. Study medications were provided by Boehringer Ingelheim Pharmaceuticals, Bristol-Myers Squibb Company, and Glaxo Wellcome Company.
PY - 2000
Y1 - 2000
N2 - Resistance mutations selected in reverse transcriptase (RT) by incompletely suppressive therapy with combination zidovudine and didanosine with or without nevirapine were identified in 141 human immunodeficiency virus type 1 isolates from peripheral blood mononuclear cells of 57 individuals in the AIDS Clinical Trials Group protocol 241. After prolonged treatment (16-48 weeks), the most common nevirapine-selected mutations were RT 181C (15/30 isolates [50%]), 190A (15/30 [50%]), and 101E (9/30 [30%]). RT 103N and 188L, which individually confer cross-resistance to all nonnucleoside RT inhibitors, were seen in a minority of viruses (6/30 [20%] and 4/30 [13%], respectively). Didanosine-resistance mutations arose rarely. A newly recognized mutation, RT 44D, was selected by the nucleosides. Two distinct zidovudine-resistance mutational patterns were noted. Mutations selected during treatment with zidovudine, didanosine, and nevirapine differed among individuals and changed over time. Resistance testing is necessary to identify which mutations are selected by nevirapine-containing combinations.
AB - Resistance mutations selected in reverse transcriptase (RT) by incompletely suppressive therapy with combination zidovudine and didanosine with or without nevirapine were identified in 141 human immunodeficiency virus type 1 isolates from peripheral blood mononuclear cells of 57 individuals in the AIDS Clinical Trials Group protocol 241. After prolonged treatment (16-48 weeks), the most common nevirapine-selected mutations were RT 181C (15/30 isolates [50%]), 190A (15/30 [50%]), and 101E (9/30 [30%]). RT 103N and 188L, which individually confer cross-resistance to all nonnucleoside RT inhibitors, were seen in a minority of viruses (6/30 [20%] and 4/30 [13%], respectively). Didanosine-resistance mutations arose rarely. A newly recognized mutation, RT 44D, was selected by the nucleosides. Two distinct zidovudine-resistance mutational patterns were noted. Mutations selected during treatment with zidovudine, didanosine, and nevirapine differed among individuals and changed over time. Resistance testing is necessary to identify which mutations are selected by nevirapine-containing combinations.
UR - http://www.scopus.com/inward/record.url?scp=0034081772&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0034081772&partnerID=8YFLogxK
U2 - 10.1086/315329
DO - 10.1086/315329
M3 - Article
C2 - 10720511
AN - SCOPUS:0034081772
SN - 0022-1899
VL - 181
SP - 904
EP - 911
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 3
ER -