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系统性红斑狼疮和混合性结缔组织病中的B细胞增殖与分化

B-cell proliferation and differentiation in systemic lupus erythematosus and mixed connective tissue disease.

作者信息

Kallenberg C G, van Dissel-Emiliani F, Huitema M G, Limburg P C, The T H

机构信息

Department of Clinical Immunology, University Hospital, Groningen, The Netherlands.

出版信息

J Clin Lab Immunol. 1988 Jun;26(2):55-61.

PMID:3264025
Abstract

Systemic lupus erythematosus (SLE) and mixed connective tissue disease (MCTD) are characterized by B-cell hyperactivity as manifested by spontaneous in vitro production of immunoglobulins (Ig), but pokeweed mitogen (PWM)-induced Ig synthesis of peripheral blood (PB) mononuclear cells, a T-cell dependent process, is markedly decreased. We analyzed the defective capacity to produce Ig in vitro in 11 patients with SLE and 11 with MCTD. PWM-activated PB T-cells, both from SLE- and MCTD-patients, did not differ from control T-cells in their capacity to produce B-cell growth factors (BCGF) and B-cell differentiation factors (BCDF). However, B-cell proliferative responsiveness to control T-cell factors was decreased compared to control B-cells (p less than 0.01). In contrast to PB B-cells splenic B-cells from a patient with MCTD who underwent splenectomy were highly responsive to T-cell factors in a dose dependent way. It is concluded that the defective PWM-induced Ig production of PB lymphocytes in SLE/MCTD is due to decreased responsiveness of PB B cells to T-cell factors. However, analysis of splenic lymphocytes may be more representative for evaluation of the immunoregulatory disturbances in these disorders.

摘要

系统性红斑狼疮(SLE)和混合性结缔组织病(MCTD)的特征是B细胞功能亢进,表现为体外自发产生免疫球蛋白(Ig),但T细胞依赖性过程——外周血(PB)单个核细胞的商陆丝裂原(PWM)诱导的Ig合成明显减少。我们分析了11例SLE患者和11例MCTD患者体外产生Ig的缺陷能力。来自SLE和MCTD患者的PWM激活的PB T细胞在产生B细胞生长因子(BCGF)和B细胞分化因子(BCDF)的能力方面与对照T细胞没有差异。然而,与对照B细胞相比,B细胞对对照T细胞因子的增殖反应性降低(p<0.01)。与PB B细胞相反,一名接受脾切除术的MCTD患者的脾B细胞以剂量依赖方式对T细胞因子高度反应。结论是,SLE/MCTD中PB淋巴细胞PWM诱导的Ig产生缺陷是由于PB B细胞对T细胞因子的反应性降低。然而,脾淋巴细胞分析可能更能代表评估这些疾病中的免疫调节紊乱。

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引用本文的文献

1
B cell activation in clinically quiescent systemic lupus erythematosus (SLE) is related to immunoglobulin levels, but not to levels of anti-dsDNA, nor to concurrent T cell activation.临床静止期系统性红斑狼疮(SLE)中的B细胞活化与免疫球蛋白水平有关,但与抗双链DNA水平无关,也与同时存在的T细胞活化无关。
Clin Exp Immunol. 1993 Jul;93(1):39-44. doi: 10.1111/j.1365-2249.1993.tb06494.x.
2
T lymphocyte activation in systemic lupus erythematosus analysed by proliferative response to nucleoplasmic proteins on nitrocellulose immunoblots.通过对硝酸纤维素免疫印迹上核质蛋白的增殖反应分析系统性红斑狼疮中的T淋巴细胞活化。
Clin Exp Immunol. 1989 Aug;77(2):168-74.
3
Cytokine-independent progression of immunoglobulin production in vitro by B lymphocytes from patients with systemic lupus erythematosus.
系统性红斑狼疮患者B淋巴细胞在体外不依赖细胞因子的免疫球蛋白产生过程
Clin Exp Immunol. 1991 Feb;83(2):274-9. doi: 10.1111/j.1365-2249.1991.tb05627.x.
4
Abnormal production of B cell growth factor in patients with systemic lupus erythematosus.系统性红斑狼疮患者B细胞生长因子的异常产生。
Clin Exp Immunol. 1992 Jul;89(1):26-31. doi: 10.1111/j.1365-2249.1992.tb06872.x.