Long-term effects of protease-inhibitor-based combination therapy on CD4 T-cell recovery in HIV-1-infected children and adolescents

被引:66
作者
Soh, CH
Oleske, JM
Brady, MT
Spector, SA
Borkowsky, W
Burchett, SK
Foca, MD
Handelsman, E
Jiménez, E
Dankner, WM
Hughes, MD
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[2] Univ Med & Dent New Jersey, Div Allergy Immunol, Newark, NJ 07103 USA
[3] Childrens Hosp, Dept Infect Dis, Columbus, OH 43205 USA
[4] Univ Calif San Diego, Dept Pediat, San Diego, CA 92103 USA
[5] NYU Med Ctr, New York, NY 10016 USA
[6] Bellevue Hosp, New York, NY USA
[7] Childrens Hosp, Boston, MA 02115 USA
[8] Childrens Hosp New York, Div Infect Dis, New York, NY USA
[9] Columbia Univ, New York, NY USA
[10] Childrens Med Ctr Brooklyn, Brooklyn, NY USA
[11] San Juan City Hosp, Rio Piedras, PR USA
[12] Duke Univ, Med Ctr, Durham, NC USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0140-6736(03)15098-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background There is limited evidence about longer-term effects of combination antiretroviral therapy that includes protease inhibitors (Pls) on the immunological status of HIV-1-infected children. Better understanding might help to resolve questions on when to initiate treatment. Methods The change in percentage of CD4-positive T lymphocytes (CD4%) was investigated in 1012 previously treated HIV-1-infected children (aged 0-17 years) who were enrolled in research clinics in the USA before 1996 and followed up to 2000. 702 started Pl-based combination therapy. Data analyses ignored subsequent treatment changes. Findings Among the 1012 children, the median CD4% increased from 22% to 28% between 1996, when Pls were first prescribed, and 2000. For the 702 who started Pl-based therapy, the mean CD4% increase after 3 years was largest among participants with the greatest immunosuppression (15.7%, 10.6%, 5.1%, and 2.0% for participants with CD4% before therapy of <5%, 5-14%, 15-24%, and ≥25%; p<0.0001). After adjustment for pre-PI CD4%, the mean increase was largest among the youngest participants (9.2%, 8.0%, and 4.3% for ages <5 years, 5-9 years, and ≥10 years; p=0.001). However, only a minority of significantly immunocompromised participants (33%, 26%, and 49% of those with pre-Pl CD4% of <5%, 5-14%, or 15-24%) achieved CD4% values above 25%, whereas 84% of those with pre-PI values above 25% maintained such values. Interpretation Although Pl-based therapy was associated with substantial improvements in CD4%, initiation before severe immunosuppression and at younger ages may be more effective for recovery or maintenance of normal CD4%. Randomised investigation of when to start combination therapy in children, particularly infants, is needed.
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页码:2045 / 2051
页数:7
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