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首页> 外文期刊>Journal of Immunological Methods >Selection and validation of antibody clones against IgG and IgA subclasses in switched memory B-cells and plasma cells
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Selection and validation of antibody clones against IgG and IgA subclasses in switched memory B-cells and plasma cells

机译:切换存储器B细胞和等离子体细胞中对IgG和IgA亚类抗体克隆的选择和验证

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The clinical value of assessing immunoglobulin (Ig)G and IgA subclasses in addition to the isotypes of soluble Igs in serum has been well established. > 20 years ago, the International Union of Immunological Societies and the World Health Organization performed collaborative studies in order to validate antibody (Ab) clones for the detection of IgG and IgA subclasses for a broad range of laboratory assays, except for flow cytometry. Here we analyzed the performance of commercially available Ab clones to detect IgG and IgA subclasses in memory B-cells and plasma cells (PCs) by flow cytometry. In a first step, 28 Ab clones were evaluated in peripheral blood from healthy donors. Only 17/28 clones showed reactivity against IgG and IgA subclasses expressed on the B-cell and PC surface membrane, including Ab clones for IgG(1) (SAG1, HP6188, HP6001 and HP6186), IgG(2) (SAG2, HP6014 and HP6002), IgG(3) (SAG3, HP6095 and HP6050), IgG(4) (SAG4), IgA(1) (SAA1, H69-11.4 and B3506B4) and IgA(2) (SAA2, 2E2, and A9604D2). In a second step, for each Ig subclass a single clone was selected according to its specificity and fluorescence intensity (resolution power), for further more detailed validation (SAG1, SAG2, SAG3, SAG4, SAA1 and SAA2). This validation process was carried out in 4 different laboratories by testing the selected Ab clones in human peripheral blood, bone marrow and tonsil samples, using different staining protocols (e.g. surface membrane and/or cytoplasmic staining). All selected Ab clones displayed strong positivity, high specificity and optimal resolution between negative and positive cells. Alternative Ab clones were also validated. Thus, our results show the feasibility of using the validated Ig subclass Ab clones in combination with other B cell-associated markers for detailed dissection of the memory B-cell and PC compartments that express distinct Ig subclasses in different human tissues.
机译:评估免疫球蛋白(IG)G和IgA亚类除了血清中可溶性Igs同样物外的临床价值已经很好地建立。 > 20年前,国际免疫社会和世界卫生组织联盟进行了合作研究,以便在流式细胞术外检测抗体(AB)克隆用于广泛的实验室测定的IgG和IgA亚类。在这里,我们通过流式细胞术分析了商业上可获得的AB克隆的性能,以通过流式细胞术检测内存B细胞和血浆细胞(PCS)中的IgG和IgA亚类。在第一步中,在来自健康供体的外周血中评估28AB克隆。仅17/28克隆显示对B细胞和PC表面膜上表达的IgG和IgA亚类的反应性,包括IgG(1)的AB克隆(SAG1,HP6188,HP6001和HP6186),IgG(2)(SAG2,HP6014和HP6002),IgG(3)(SAG3,HP6095和HP6050),IgG(4)(SAG4),IgA(1)(SAA1,H69-11.4和B3506B4)和IgA(2)(SAA2,2E2和A9604D2)。在第二步中,对于每个IG子类,根据其特异性和荧光强度(分辨率电源)选择单个克隆,用于进一步更详细的验证(SAG1,SAG2,SAG3,SAG4,SAA1和SAA2)。通过使用不同的染色方案(例如表面膜和/或细胞质染色),通过测试人外周血,骨髓和扁桃体样品中所选择的AB克隆,在4种不同的实验室中进行了该验证过程。所有选择的AB克隆显示出强阳性,高特异性和阳性细胞之间的最佳分辨率。还验证了替代AB克隆。因此,我们的结果表明,使用验证的Ig亚类AB克隆与其他B细胞相关标记组合的可行性,用于详细解剖储存B细胞和PC隔室,其在不同人体组织中表达不同的Ig亚类。

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