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急性多发性神经根神经炎(格林-巴利综合征)中的淋巴细胞亚群及抑制细胞活性

Lymphocyte subpopulations and suppressor cell activity in acute polyradiculoneuritis (Guillain-Barré syndrome).

作者信息

Hughes R A, Aslan S, Gray I A

出版信息

Clin Exp Immunol. 1983 Mar;51(3):448-54.

Abstract

Ficoll-Triosil separated peripheral blood mononuclear (PBM) cells were analysed by fluorescent microscopy with Ortho monoclonal antisera to T cells (OKT3+) helper cells (OKT4+) and suppressor cytotoxic cells (OKT8+) and with polyclonal antiserum to surface immunoglobulin. Twenty-five normal subjects, 16 patients with acute polyradiculoneuritis (Guillain-Barré syndrome, AP) and 10 patients with other neurological diseases were studied. The percentages of OKT3+, OKT4+ and immunoglobulin bearing cells were similar in the three patient groups but the percentage of OKT8+ cells was reduced to 13.5 +/- 4.1 (mean +/- s.d.) compared with 19.4 +/- 4.9 in the normal subjects and 18.5 +/- 3.1 in the patients with other neurological diseases. The ratio of OKT4+/OKT8+ cells was correspondingly increased to 3.5 +/- 2.1 compared with 2.1 +/- 0.5 in the normal subjects and 2.1 +/- 0.4 in the patients with other neurological diseases. In one test of suppressor cell function Con A incubated mitomycin treated PBM cells were added to autologous PBM cells stimulated with Con A to compare the degree of suppression with that produced by control incubated mitomycin treated cells (Con A suppression test). In a second test of suppressor cell function short lived suppressor cell (SLS) activity was assayed by comparing PBM stimulation by Con A added at the start of culture with that produced by Con A added after 24 hr. Neither test revealed any significant differences between AP patients and control subjects.

摘要

用Ficoll-Triosil分离的外周血单个核(PBM)细胞,通过荧光显微镜,使用针对T细胞(OKT3 +)、辅助性T细胞(OKT4 +)和抑制性细胞毒性细胞(OKT8 +)的Ortho单克隆抗血清以及针对表面免疫球蛋白的多克隆抗血清进行分析。研究了25名正常受试者、16名急性多发性神经根神经炎患者(格林-巴利综合征,AP)和10名患有其他神经系统疾病的患者。三组患者中OKT3 +、OKT4 +和携带免疫球蛋白细胞的百分比相似,但OKT8 +细胞的百分比降至13.5±4.1(平均值±标准差),而正常受试者为19.4±4.9,患有其他神经系统疾病的患者为18.5±3.1。OKT4 + /OKT8 +细胞的比例相应增加至3.5±2.1,而正常受试者为2.1±0.5,患有其他神经系统疾病的患者为2.1±0.4。在一项抑制细胞功能测试中,将经丝裂霉素处理的伴刀豆球蛋白A(Con A)孵育的PBM细胞加入到经Con A刺激的自体PBM细胞中,以比较抑制程度与经对照孵育的丝裂霉素处理细胞所产生的抑制程度(Con A抑制试验)。在第二项抑制细胞功能测试中,通过比较培养开始时添加的Con A与培养24小时后添加的Con A对PBM的刺激作用,测定短期抑制细胞(SLS)活性。两项测试均未显示AP患者与对照受试者之间有任何显著差异。

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