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系统性红斑狼疮中自发免疫球蛋白A分泌及缺乏有丝分裂原反应性B细胞

Spontaneous immunoglobulin A secretion and lack of mitogen-responsive B cells in systemic lupus erythematosus.

作者信息

Saiki O, Saeki Y, Kishimoto S

出版信息

J Clin Invest. 1985 Nov;76(5):1865-70. doi: 10.1172/JCI112180.

Abstract

In an analysis of lymphocyte functions of systemic lupus erythematosus (SLE) patients, B cell abnormalities such as a lack of mitogen-responsive B cells and a predominance of spontaneous IgA-secreting cells (SC) were found. Lymphocyte functions of 20 SLE patients were studied. Impaired proliferative response to B cell mitogen, Staphylococcus aureus strain Cowan I (Cowan I), was observed, whereas the response to T cell mitogen phytohemagglutinin was normal. High levels of spontaneous IgA-SC were observed in SLE patients (greater than 10(2) cells/10(4) peripheral blood mononuclear cells [PBMC]), whereas spontaneous IgM-, IgG-, or IgE-SC were not proportionately increased. The number of spontaneous IgA-SC decreased with time in culture and became undetectable by day 5 of culture. In contrast, spontaneous immunoglobulin- (IgM, IgG, and IgA) SC were not observed in healthy volunteers (less than 10 cells/10(4) PBMC). Moreover, in SLE patients failure of induction of immunoglobulin-secreting cells (ISC) was observed when B cells were stimulated by Cowan I and B cell differentiation factor at any day tested, whereas ISC were induced in healthy volunteers on day 6 of culture. Depletion of T cells or macrophages did not affect the results obtained. These results suggest that the abnormalities observed in SLE B cells are not due to the in vitro direct effects of suppressor macrophages or suppressor T cells, and that the condition of the predominance of spontaneous IgA-SC and the unresponsiveness to exogenous stimulation may be emblematic of hyperactive B cells in SLE.

摘要

在一项对系统性红斑狼疮(SLE)患者淋巴细胞功能的分析中,发现了B细胞异常,如缺乏有丝分裂原反应性B细胞和自发性分泌IgA的细胞(SC)占优势。研究了20例SLE患者的淋巴细胞功能。观察到对B细胞有丝分裂原金黄色葡萄球菌Cowan I株(Cowan I)的增殖反应受损,而对T细胞有丝分裂原植物血凝素的反应正常。SLE患者中观察到高水平的自发性IgA-SC(大于10²细胞/10⁴外周血单个核细胞[PBMC]),而自发性IgM-、IgG-或IgE-SC没有相应增加。自发性IgA-SC的数量在培养过程中随时间减少,到培养第5天时变得无法检测到。相比之下,健康志愿者中未观察到自发性免疫球蛋白(IgM、IgG和IgA)SC(小于10细胞/10⁴PBMC)。此外,在SLE患者中,当在任何测试日用Cowan I和B细胞分化因子刺激B细胞时,观察到免疫球蛋白分泌细胞(ISC)诱导失败,而健康志愿者在培养第6天诱导出了ISC。T细胞或巨噬细胞的清除不影响所得结果。这些结果表明,SLE B细胞中观察到的异常不是由于抑制性巨噬细胞或抑制性T细胞的体外直接作用,并且自发性IgA-SC占优势和对外源刺激无反应的情况可能是SLE中B细胞过度活跃的标志。

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1
AUTOANTIBODIES AND DISEASE.自身抗体与疾病
Adv Immunol. 1964;27:351-95. doi: 10.1016/s0065-2776(08)60711-7.

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