Landay A, Ho J L, Hom D, Russell T, Zwerner R, Minuty J G, Kataaha P, Mmiro F, Jackson B
Department of Immunology/Microbiology, Rush-Presbyterian-St Luke's Medical Center, Chicago, Illinois 60612.
AIDS. 1993 Dec;7(12):1565-8. doi: 10.1097/00002030-199312000-00004.
To evaluate a manual method (Cytosphere) for quantifying CD4+ T-cell numbers.
Cross-sectional study of HIV-1-seronegative and HIV-1-seropositive individuals evaluated for absolute CD4 counts by both standardized flow cytometric measurements and manual Cytosphere technology using a hemacytometer.
University research hospitals in both the United States and Africa.
PATIENTS, PARTICIPANTS: Blood specimens from 382 patients were evaluated. These were broken down into 294 samples obtained from HIV-1-seropositive patients and 88 samples obtained from HIV-1-seronegative patients.
None.
Absolute CD4 cell number.
Evaluation of samples obtained from HIV-1 patients in both the United States and Africa demonstrated an overall correlation of the Cytosphere assay with flow cytometry of 0.912 (95% confidence interval, 0.895-0.928; P < 0.001). When samples were stratified based on CD4+ T-cell counts determined by flow cytometry, the Cytosphere assay had a 96% predictive value for correctly identifying individuals with CD4 T-cell counts > 200 x 10(6)/l and a 92% predictive value for correctly identifying individuals with CD4 T-cell counts < 200 x 10(6)/l.
This assay appears to have the potential for the quantitation of CD4 cells in the limited laboratory facilities in developing countries and to have a strong correlation with standard flow cytometric technology.
评估一种用于定量CD4+ T细胞数量的手工方法(血细胞球计数法)。
对HIV-1血清阴性和HIV-1血清阳性个体进行横断面研究,通过标准化流式细胞术测量和使用血细胞计数板的手工血细胞球计数技术评估绝对CD4计数。
美国和非洲的大学研究医院。
患者、参与者:对382例患者的血液标本进行评估。这些标本分为从HIV-1血清阳性患者获得的294份样本和从HIV-1血清阴性患者获得的88份样本。
无。
绝对CD4细胞数量。
对在美国和非洲从HIV-1患者获得的样本进行评估,结果显示血细胞球计数法与流式细胞术的总体相关性为0.912(95%置信区间,0.895 - 0.928;P < 0.001)。当根据流式细胞术确定的CD4+ T细胞计数对样本进行分层时,血细胞球计数法对于正确识别CD4 T细胞计数>200×10⁶/l的个体具有96%的预测价值,对于正确识别CD4 T细胞计数<200×10⁶/l的个体具有92%的预测价值。
该检测方法似乎有潜力在发展中国家有限的实验室设施中对CD4细胞进行定量,并且与标准流式细胞术技术有很强的相关性。