首页> 外文期刊>Cytometry: The Journal of the Society for Analytical Cytology >Detection of apoptotic T lymphocytes in peripheral blood of human immunodeficiency virus (HIV)-infected subjects by Apostain
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Detection of apoptotic T lymphocytes in peripheral blood of human immunodeficiency virus (HIV)-infected subjects by Apostain

机译:Apostain检测人免疫缺陷病毒(HIV)感染者外周血中凋亡的T淋巴细胞

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Apoptosis has been indicated as a mechanism of T cell depletion in HIV-infected subjects and useful in monitoring disease progression. We investigated for the presence of apoptotic T lymphocytes in 130 HIV subjects in various stages of disease by the newly developed cell permeant DNA dye Apostain, Blood was collected in EDTA, lysed in buffered ammonium chloride, fixed in freshly prepared 1% paraformaldehyde and stored in aliquots at -80 degrees C. Samples were thawed and double stained with FITC conjugated-CD3 monoclonal antibody and Apostain, Flow cytometry was then performed and T cells gated on a CD3 versus side scatter dot plot. Normal samples treated in the same manner served to establish the boundary separating non-apoptotic from apoptotic cells. There was no statistically significant association between the proportion of subjects with detectable apoptotic cells and CDC clinical categories A, B and C at the time of admission to the study, although a trend toward a lower apoptotic rate in category A (A= 29%, B=40% and C=41%) was noticed. Conversely, CDC T cell categories 2 and 3 contained significantly higher proportions of Apostain positive patients (1=6%, 2=32% and 3=49%, P=0.072, by chi(2) test), Most importantly, Apostain test identified subjects at risk of disease progression during a 3.5-7 months follow-up in CDC category B and 2 (P=0.008 and P=0.0003, by Fisher's exact test, respectively). a similar, albeit not statistically significant trend was observed also in the other categories, Not requiring extensive manipulation of fresh samples nor cumbersome culture techniques, Apostain test appears suitable for identifying HIV subjects at higher risk of disease progression in clinical settings. (C) 2000 Wiley-Liss, Inc. [References: 19]
机译:已经表明凋亡是HIV感染的受试者中T细胞耗竭的机制,并且可用于监测疾病的进展。我们通过新开发的细胞渗透性DNA染料Apostain调查了130个处于疾病各个阶段的HIV受试者中凋亡性T淋巴细胞的存在,将血液收集到EDTA中,在缓冲的氯化铵中溶解,固定在新鲜制备的1%多聚甲醛中,并保存在在-80℃下等分试样。将样品解冻并用FITC缀合的CD3单克隆抗体和Apostain进行双染色,然后进行流式细胞术,并在CD3对侧向散射点图上对T细胞进行门控。以相同方式处理的正常样品用于建立区分非凋亡细胞与凋亡细胞的边界。进入研究时,具有可检测凋亡细胞的受试者比例与CDC临床A,B和C类之间没有统计学上的显着相关性,尽管A类中凋亡率呈下降趋势(A = 29%,观察到B = 40%和C = 41%。相反,CDC T细胞类别2和3包含更高比例的Apostain阳性患者(通过chi(2)测试,分别为1 = 6%,2 = 32%和3 = 49%,P = 0.072),最重要的是,Apostain测试确定了在CDC B类和2类CDC的3.5-7个月随访期间有疾病进展风险的受试者(分别通过Fisher精确检验分别为P = 0.008和P = 0.0003)。尽管在其他类别中也没有观察到类似的趋势,但在统计学上也没有显着趋势。不需要大量操作新鲜样品或繁琐的培养技术,Apostain测试似乎适用于在临床环境中鉴定出具有较高疾病进展风险的HIV受试者。 (C)2000 Wiley-Liss,Inc. [参考:19]

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