人类免疫缺陷病毒(HIV)感染者外周血中凋亡T淋巴细胞的检测。

Cytometry Pub Date : 2000-02-15
A Kunkl, M Paola Terranova, C Ferlini, G Astegiano, G Mazzarello, G Scambia, A Fattorossi
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引用次数: 0

摘要

细胞凋亡已被证明是hiv感染者T细胞耗竭的一种机制,并可用于监测疾病进展。我们通过新开发的细胞渗透DNA染色Apostain研究了130例不同阶段HIV患者中凋亡T淋巴细胞的存在。采集血液于EDTA中,在缓冲氯化铵中裂解,在新鲜制备的1%多聚甲醛中固定,在-80℃下分装保存。样品解冻,用FITC偶联cd3单克隆抗体和Apostain双染色。然后进行流式细胞术,并在CD3与侧散点图上对T细胞进行门控。以同样方式处理的正常样品用于建立非凋亡细胞与凋亡细胞的边界。入组时可检测到凋亡细胞的受试者比例与CDC临床分类A、B、C之间无统计学意义的相关性,但A类的凋亡率有较低的趋势(A= 29%, B=40%, C=41%)。相反,CDC T细胞2、3类Apostain阳性患者比例显著高于CDC T细胞2、3类(chi(2)检验,1=6%,2=32%,3=49%,P=0.072)。最重要的是,Apostain试验在3.5-7个月的CDC B类和2类随访中确定了有疾病进展风险的受试者(分别通过Fisher精确检验P=0.008和P=0.0003)。在其他类别中也观察到类似的趋势,尽管统计上不显著。Apostain测试不需要大量的新鲜样本操作,也不需要繁琐的培养技术,似乎适合在临床环境中识别疾病进展风险较高的HIV受试者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Detection of apoptotic T lymphocytes in peripheral blood of human immunodeficiency virus (HIV)-infected subjects by apostain.

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.

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