Combination treatment with zidovudine, didanosine, and nevirapine in infants with human immunodeficiency virus type 1 infection

被引:159
作者
Luzuriaga, K
Bryson, Y
Krogstad, P
Robinson, J
Stechenberg, B
Lamson, M
Cort, S
Sullivan, JL
机构
[1] UNIV CALIF LOS ANGELES, DEPT PEDIAT, LOS ANGELES, CA 90024 USA
[2] UNIV CONNECTICUT, SCH MED, DEPT PEDIAT, FARMINGTON, CT 06032 USA
[3] BAYSTATE MED CTR, DEPT PEDIAT, SPRINGFIELD, MA 01199 USA
[4] BOEHRINGER INGELHEIM PHARMACEUT INC, RIDGEFIELD, CT 06877 USA
关键词
D O I
10.1056/NEJM199705083361902
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background In infants and children with maternally acquired human immunodeficiency virus type 1 (HIV-1) infection, treatment with a single antiretroviral agent has limited efficacy. We evaluated the safety and efficacy of a three-drug regimen in a small group of maternally infected infants. Methods Zidovudine, didanosine, and nevirapine were administered in combination orally to eight infants 2 to 16 months of age. The efficacy of antiretroviral treatment was evaluated by serial measurements of plasma HIV-1 RNA, quantitative plasma cultures, and quantitative cultures of peripheral-blood mononuclear cells. Results The three-drug regimen was well tolerated, without clinically important adverse events. Within four weeks, there were reductions in plasma levels of HIV-1 RNA of at least 96 percent (1.5 log) in seven of the eight study patients. Over the 6-month study period, replication of HIV-1 was controlled in two infants who began therapy at 2 1/2 months of age. Plasma RNA levels were reduced by 0.5 to 1.5 log in five of the other six infants. Conclusions Although further observations are needed, it appears that in infants with maternally acquired HIV-1 infection, combined treatment with zidovudine, didanosine, and nevirapine is well tolerated and has sustained efficacy against HIV-1. (C)1997, Massachusetts Medical Society.
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页码:1343 / 1349
页数:7
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