Predictors of immunological failure after initial response to highly active antiretroviral therapy in HIV-1-infected adults: A EuroSIDA study

被引:48
作者
Dragsted, UB
Mocroft, A
Vella, S
Viard, JP
Hansen, ABE
Panos, G
Mercey, D
Machala, L
Horban, A
Lundgren, JD
机构
[1] Hvidovre Univ Hosp, Copenhagen HIV Programme, DK-2650 Hvidovre, Denmark
[2] Rigshosp, DK-2100 Copenhagen, Denmark
[3] Royal Free Hosp, London NW3 2QG, England
[4] UCL, Sch Med, London W1N 8AA, England
[5] Ist Super Sanita, I-00161 Rome, Italy
[6] Hop Necker Enfants Malad, Paris, France
[7] 1st IKA Hosp, Athens, Greece
[8] Fac Hosp Bulovka, Prague, Czech Republic
[9] Cent Diagnost & Terapii AIDS, Warsaw, Poland
来源
JOURNAL OF INFECTIOUS DISEASES | 2004年 / 190卷 / 01期
关键词
D O I
10.1086/420786
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Factors that determine the immunological response to highly active antiretroviral therapy (HAART) are poorly defined. Objective. Our aim was to investigate predictors of immunological failure after initial CD4(+) response. Methods. Data were from EuroSIDA, a prospective, international, observational human immunodeficiency virus (HIV) type 1 cohort. Results. Of 2347 patients with an increase in CD4(+) cell count greater than or equal to100 cells/muL within 6-12 months of the initiation of HAART, 550 (23%) subsequently experienced immunological failure (CD4(+) count less than or equal to the pre-HAART value). The incidence of failure was 11.6 incidences/100 person-years of follow-up (95% confidence interval [CI], 10.2-13.4) during the first 12 months and decreased significantly over time (P < .0001). Independent predictors of immunological failure were pre-HAART CD4(+) cell count (per 50% higher; relative hazard [RH], 2.05; 95% CI, 1.83-2.31; P < .0001), time-updated virus load (per 1 log(10) higher; RH, 1.77; 95% CI, 1.64-1.92; P < .0001), and HIV-1 risk behavior (for a global comparison of risk groups). Conclusion. The risk of immunological failure in patients with an immunological response to HAART diminishes with a longer time receiving treatment and is associated with pretreatment CD4(+) cell count, ongoing viral replication, and intravenous drug use.
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页码:148 / 155
页数:8
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