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格林-巴利综合征和慢性特发性脱髓鞘性多发性神经根神经病中的T淋巴细胞活化抗原

T lymphocyte activation antigens in Guillain-Barré syndrome and chronic idiopathic demyelinating polyradiculoneuropathy.

作者信息

Taylor W A, Hughes R A

机构信息

Neurology Department, United Medical, School of Guy's Hospital, London, U.K.

出版信息

J Neuroimmunol. 1989 Sep;24(1-2):33-9. doi: 10.1016/0165-5728(89)90095-7.

DOI:10.1016/0165-5728(89)90095-7
PMID:2808686
Abstract

Activated circulating T lymphocytes were measured in ten patients with Guillain-Barré syndrome (GBS) and in ten with chronic idiopathic demyelinating polyradiculoneuropathy (CIDP), each paired with an age- and sex-matched healthy control. Activated T cells were identified by double labelling with phycoerythrin-conjugated anti-CD3 antibody and biotinylated antibodies to activation antigens: human leucocyte antigen (HLA)-DR, transferrin receptor (TFR) or interleukin-2 receptor (IL-2R) visualised with an avidin-biotin-fluorescein system. The frequency of activated T cells was increased in the GBS group. The median of the DR-positive T cells in the patients was 3.4% (range 0.5-9.4%), compared with 1.4% (range 0-4.3%) in the controls (P less than 0.01). For TFR the corresponding medians were 3.3% (range 0.5-6.2%) in the patients and 0% (range 0-2.5%) in the controls (P less than 0.01), and for IL-2R 3.7% (range 0-6.0%) in the patients compared with 0% (range 0-2.9%) in the controls (P less than 0.01). In the CIDP group the median percentage of activated T cells was also increased but the differences were less significant: for DR, patients 2.4% (range 0-3.8%), controls 0.5% (range 0-2.0%, P less than 0.05); for TFR, patients 0% (range 0-5.3%), controls 0% (range 0-1.0%, not significant), and for IL-2R, patients 0% (range 0-2.5%), controls 0% (range 0-0.5%, not significant). The activated cells might be directed against microbial antigens encountered during the infection preceding GBS, autoantigens, bacterial antigens encountered during concurrent infection, or a combination of these.

摘要

对10例吉兰 - 巴雷综合征(GBS)患者和10例慢性特发性脱髓鞘性多发性神经根神经病(CIDP)患者进行了活化循环T淋巴细胞检测,每组均配对一名年龄和性别匹配的健康对照。通过用藻红蛋白偶联的抗CD3抗体和生物素化的活化抗原抗体进行双重标记来鉴定活化的T细胞:人白细胞抗原(HLA)-DR、转铁蛋白受体(TFR)或白细胞介素-2受体(IL-2R),使用抗生物素蛋白-生物素-荧光素系统进行可视化。GBS组中活化T细胞的频率增加。患者中DR阳性T细胞的中位数为3.4%(范围0.5 - 9.4%),而对照组为1.4%(范围0 - 4.3%)(P小于0.01)。对于TFR,患者和对照组的相应中位数分别为3.3%(范围0.5 - 6.2%)和0%(范围0 - 2.5%)(P小于0.01),对于IL-2R,患者为3.7%(范围0 - 6.0%),对照组为0%(范围0 - 2.9%)(P小于0.01)。在CIDP组中,活化T细胞的中位数百分比也有所增加,但差异不太显著:对于DR,患者为2.4%(范围0 - 3.8%),对照组为0.5%(范围0 - 2.0%,P小于0.05);对于TFR,患者为0%(范围0 - 5.3%),对照组为0%(范围0 - 1.0%,无显著性差异),对于IL-2R,患者为0%(范围0 - 2.5%),对照组为0%(范围0 - 0.5%,无显著性差异)。活化细胞可能针对GBS发病前感染期间遇到的微生物抗原、自身抗原、并发感染期间遇到的细菌抗原或这些抗原的组合。

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