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A comparison of two 125I C1q binding tests to detect soluble immune complexes in serum of patients with malignant disease.

机译:两种125I C1q结合试验检测恶性疾病患者血清中可溶性免疫复合物的比较。

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摘要

The 125I C1q deviation test and the modified 125I C1q PEG precipitation test were compared in their ability to detect soluble immune complexes in serum using a model system of HSA-rabbit-anti-HSA, and were then applied to sera collected from patients with malignant and non-malignant conditions. Despite close agreement in the model system, the two tests gave divergent results for the presence of C1q binding substances in individual serum samples collected from patients. The inherent complexities of interpreting C1q binding in serum, in terms of the presence of soluble immune complexes, makes it questionable whether either test can be relied upon to provide a means of identifying these complexes in the sera from patients with malignant disease.
机译:使用HSA-兔-抗-HSA模型系统比较了125I C1q偏差测试和改良的125I C1q PEG沉淀测试在血清中检测可溶性免疫复合物的能力,然后将其应用于从恶性和恶性肿瘤患者中收集的血清非恶性疾病。尽管在模型系统中达成了一致,但是对于从患者收集的各个血清样本中存在的C1q结合物质,这两个测试给出了不同的结果。就可溶性免疫复合物的存在而言,解释血清中C1q结合的内在复杂性使人们怀疑是否可以依靠任何一种测试来提供从恶性疾病患者中鉴定血清中这些复合物的手段。

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