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评价普通变异性免疫缺陷患者 B 淋巴细胞中的类别转换重组。

Evaluation of class switch recombination in B lymphocytes of patients with common variable immunodeficiency.

机构信息

Department of Immunology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

出版信息

J Immunol Methods. 2013 Aug 30;394(1-2):94-9. doi: 10.1016/j.jim.2013.05.008. Epub 2013 May 25.

DOI:10.1016/j.jim.2013.05.008
PMID:23714403
Abstract

Common variable immunodeficiency (CVID) is a heterogeneous group of disorders characterized by hypogammaglobulinemia and recurrent bacterial infections. Impaired antibody production in these patients is due to defect in B-cell differentiation into specific plasma cells. Class switch recombination (CSR), which plays a critical role in the production of different immunoglobulin isotypes, may be defective in a group of CVID patients. The aim of this study was to investigate the CSR process in B cells of CVID patients, by evaluating the expression of IgE mRNA and production of its protein in an IgE inductive medium. Peripheral blood mononuclear cells (PBMCs) from 29 CVID patients and 21 healthy controls were isolated and cultured in the presence of rhIL-4 and CD40L. IgE mRNA and IgE protein were measured by RT-PCR and ELISA techniques, respectively. Normal production of IgE mRNA was recorded in 23 out of 29 patients (79.31%) as well as all controls; while the remaining 6 patients (20.69%) were unable to express IgE mRNA indicating a defect in CSR. PBMCs of 16 out of 29 patients (55.2%) could not produce normal amounts of IgE compared with controls, after being stimulated by IL-4 and CD40L. Post B cell stimulation IgE production was impaired in about half of studied CVID patients. Defects in processes occur following the CSR process such as IgE mRNA transcription, protein production, and secretion can be the causative mechanism of CVID in patients with normal mRNA expression of the immunoglobulin but impaired protein production. Determination of these defects can help to clarify the various underlying mechanisms responsible for the development of CVID.

摘要

普通变异性免疫缺陷症(CVID)是一组异质性疾病,其特征为低丙种球蛋白血症和反复细菌感染。这些患者的抗体产生受损是由于 B 细胞分化为特定浆细胞的缺陷所致。类别转换重组(CSR)在产生不同免疫球蛋白同种型方面起着关键作用,在一组 CVID 患者中可能存在缺陷。本研究旨在通过评估 IgE 诱导培养基中 IgE mRNA 的表达及其蛋白的产生,来研究 CVID 患者 B 细胞的 CSR 过程。从 29 名 CVID 患者和 21 名健康对照者中分离出外周血单核细胞(PBMC),并在 rhIL-4 和 CD40L 的存在下进行培养。通过 RT-PCR 和 ELISA 技术分别测量 IgE mRNA 和 IgE 蛋白。在 29 名患者中的 23 名(79.31%)以及所有对照者中均记录到正常的 IgE mRNA 产生;而其余 6 名患者(20.69%)无法表达 IgE mRNA,表明 CSR 存在缺陷。与对照者相比,在 IL-4 和 CD40L 刺激后,29 名患者中的 16 名(55.2%)的 PBMC 无法产生正常量的 IgE。大约一半的研究 CVID 患者在 B 细胞刺激后 IgE 产生受损。CSR 过程后可能会出现 IgE mRNA 转录、蛋白产生和分泌等过程的缺陷,这可能是导致具有正常免疫球蛋白 mRNA 表达但蛋白产生受损的 CVID 患者的致病机制。确定这些缺陷有助于阐明导致 CVID 发展的各种潜在机制。

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