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人类免疫缺陷病毒感染的儿科患者单核细胞中磷酸化齐多夫定的浓度。

Phosphorylated zidovudine concentrations in mononuclear cells in pediatric patients with human immunodeficiency virus infections.

作者信息

Wintermeyer S M, Nahata M C, Brady M T, Sobol B J, Baker R C, Hunkler J A, McOwen N M

机构信息

Children's Medical Center of Northwest Ohio, Toledo, USA.

出版信息

Pediatr AIDS HIV Infect. 1997 Apr;8(2):120-6.

Abstract

PURPOSE

The efficacy of zidovudine (ZDV) in patients with HIV-1 infection may decrease over time due to its decreased activation. The objectives of this study were to determine ZDV concentrations in plasma, active phosphorylated zidovudine (pZDV) concentrations in mononuclear cells, and assess the markers of immune function and drug toxicity during extended therapy.

METHODS

Pediatric patients (aged 3 months to 18 years) with HIV-1-infection were enrolled in the study. For each patient, one blood sample was collected at each of eight routine visits to measure plasma ZDV and ZDV concentrations by a radioimmunoassay. Data including demographic information, immunological markers (CD2+, CD3+, CD4+, CD5+/19+, CD8+, CD16+, CD19+, CD38+/8+ lymphocytes), hematologic function (absolute neutrophil count, white blood cell with differential, hemoglobin, and red blood cell count), concurrent medications, and dosage regimens were obtained.

RESULTS

The data from 13 patients were as follows: age: 2-18 years; range of ZDV dose: 76-238 mg/m2, total ZDV daily dosage: 264-720 mg/m2; duration of ZDV therapy prior to study: 1 to 37 months; time in study: 180-394 days; plasma ZDV concentration range: 5-1021 ng/ml; and pZDV concentration range: 0-5.382 pmol/10(6) cells. Both plasma ZDV and intracellular pZDV concentrations had a marked inter- and intrapatient variability. The pZDV concentrations decreased significantly over time in one pediatric patient (p < 0.05), tended to decrease but not significantly in three patients, and no decrease was detected in nine patients due to high variability. In our population, neither immunological nor drug toxicity markers changed over time.

CONCLUSIONS

Marked inter- and intrapatient variability in pZDV concentrations was observed. The ability to phosphorylate ZDV, however, did not appear to change significantly in 12 of 13 pediatric patients with HIV-1 infection during the study period of 6-13 months.

摘要

目的

齐多夫定(ZDV)在HIV-1感染患者中的疗效可能会随着时间推移因其活化作用降低而下降。本研究的目的是确定血浆中的ZDV浓度、单核细胞中活性磷酸化齐多夫定(pZDV)的浓度,并评估长期治疗期间的免疫功能标志物和药物毒性。

方法

将HIV-1感染的儿科患者(年龄3个月至18岁)纳入研究。对于每位患者,在八次常规就诊时各采集一份血样,通过放射免疫测定法测量血浆ZDV和pZDV浓度。获取的数据包括人口统计学信息、免疫标志物(CD2 +、CD3 +、CD4 +、CD5 + / 19 +、CD8 +、CD16 +、CD19 +、CD38 + / 8 +淋巴细胞)、血液学功能(绝对中性粒细胞计数、白细胞分类、血红蛋白和红细胞计数)、同时服用的药物以及给药方案。

结果

13例患者的数据如下:年龄2至18岁;ZDV剂量范围:76 - 238mg/m²,ZDV每日总剂量:264 - 720mg/m²;研究前ZDV治疗持续时间:1至37个月;研究时间:180 - 394天;血浆ZDV浓度范围:5 - 1021ng/ml;pZDV浓度范围:0 - 5.382pmol / 10⁶细胞。血浆ZDV和细胞内pZDV浓度在患者间和患者内均存在显著差异。一名儿科患者的pZDV浓度随时间显著下降(p < 0.05),三名患者有下降趋势但不显著,九名患者因变异性高未检测到下降。在我们的研究人群中,免疫标志物和药物毒性标志物均未随时间变化。

结论

观察到pZDV浓度在患者间和患者内存在显著差异。然而,在6至13个月的研究期间,13例HIV-1感染儿科患者中有12例磷酸化ZDV的能力似乎没有显著变化。

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