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A paraprotein in severe combined immunodefeciency disease detected by immunoelectrophoretic analysis of plasma.

机译:通过血浆免疫电泳分析检测到的重症合并免疫缺陷疾病中的一种副蛋白。

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摘要

A qualitative study was made of the plasma immunoglobulins of a child with severe combined immunodeficiency. By immunoelectrophoresis an immunoglobulin with an abnormal electrophoretic mobility was detected. This protein possessed mu heavy chain determinants, gave no detectable reaction with antisera specific for light chains, was of a relatively small molecular size, and was probably not composed of subunits held together by easily reduced disulfide bonds. The light chains that were present in this patient's plasma had a homogeneous electrophoretic mobility. The patient's plasma also contained at least two other immunoglobulins whose antigenic identity could not be established. One of these was abnormal in its electrophoretic mobility. The presence of the abnormal protein with mu determinants in the plasma of the second unrelated child with a similar disease suggests that the detection of this protein may have implications for the diagnosis or classification of immunodeficiency diseases.
机译:对患有严重合并免疫缺陷的儿童的血浆免疫球蛋白进行了定性研究。通过免疫电泳检测到具有异常电泳迁移率的免疫球蛋白。该蛋白具有μ个重链决定簇,与轻链特异性抗血清没有可检测到的反应,分子量相对较小,并且可能不是由容易还原的二硫键结合在一起的亚基组成。该患者血浆中存在的轻链具有均一的电泳迁移率。患者的血浆中还含有至少两种其他无法确定其抗原性的免疫球蛋白。其中之一是其电泳迁移率异常。在患有相似疾病的第二个无关儿童的血浆中存在具有mu决定簇的异常蛋白,这表明该蛋白的检测可能对免疫缺陷疾病的诊断或分类有影响。

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