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Increased IgM and IgM immune complex-like material in the circulation of renal transplant recipients with primary cytomegalovirus infections.

机译:患有原发性巨细胞病毒感染的肾移植受者的循环中IgM和IgM免疫复合物样物质的含量增加。

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摘要

Twelve of 60 consecutive adult recipients of cadaver kidney transplants had increased polyethyleneglycol (PEG) precipitable IgM immune complex-like material in their circulation in the first 4 months after transplantation. All 10 recipients with primary CMV and two of four with secondary CMV infections had significant elevations in PEG precipitable IgM that coincided with rises in their CMV antibody titres. Ultracentrifuge analysis demonstrated two peaks of PEG precipitable material with sedimentation rates of about 20S and 40S. Total IgM immunoglobulin levels also were increased in transplant recipients with CMV infections, but this was less specific and occurred in patients without CMV infections. The Clq binding assay, which is more sensitive for IgG than IgM containing complexes, was positive in only three of 10 patients with primary CMV and none of four with secondary CMV. Granular deposits of IgM, but not IgG, were detected in the glomeruli of six of seven transplants biopsied during CMV infection. The PEG-IgM assay was not influenced by rejection or prednisone therapy. Thus, transplant patients, who develop primary CMV infections, produce elevated levels of circulating IgM and IgM immune complex-like material. These findings may help to differentiate CMV infection from transplant rejection as well as to increase our understanding of the special pathogenic properties of CMV in transplant recipients.
机译:在尸体肾脏移植的60位连续成人接受者中,有12位在移植后的前4个月血液中的聚乙二醇(PEG)可沉淀的IgM免疫复合物样物质增加。所有10名原发性CMV感染者和4名继发性CMV感染者中有2名的PEG可沉淀IgM显着升高,这与他们的CMV抗体滴度升高相吻合。超速离心分析显示了PEG可沉淀物质的两个峰,沉降速率约为20S和40S。总的IgM免疫球蛋白水平在CMV感染的移植接受者中也增加了,但是特异性较低,发生在没有CMV感染的患者中。 Clq结合测定法对IgG的敏感性高于含IgM的复合物,在10例原发性巨细胞病毒患者中只有3例呈阳性,而继发CMV的4例患者均无阳性。在CMV感染期间进行活检的7例移植物中,有6例的肾小球中检测到了IgM颗粒沉积物,但没有IgG。 PEG-IgM分析不受排斥或泼尼松治疗的影响。因此,发生原发性CMV感染的移植患者产生升高水平的循环IgM和IgM免疫复合物样物质。这些发现可能有助于将CMV感染与移植排斥反应区分开来,并有助于我们了解CMV在移植受体中的特殊致病特性。

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