Indirect quenching fluororeceptor assay of anti-AChR antibodies.

M Messripour, S Moein
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引用次数: 2

Abstract

A fluororeceptor assay (FRA) has been developed for the determination of antibodies against acetylcholine receptor (AChR), employing an antifluorescein serum and fluorescein-labeled AChR. Antiserum raised against rat muscle AChR in rabbit and the labeled AChR are incubated with antifluorescein serum at room temperature. At high levels of anti-AChR, binding of the labeled AChR prevented subsequent binding of the fluorescein groups by antifluorescein, resulting in little change in the signals of the label. Conversely, at low levels of anti-AChR, the free fraction of the labeled AChR is available to be bound by antifluorescein, which markedly reduced fluorescence intensity of the label. Thus, the fluorescence intensity of the assay mixture directly reflects the amount of anti-AChR antibodies in the serum. It is concluded that the availability of fluorescein-labeled AChR and the antibody directed against it permit measurement of anti-AChR antibodies in human myasthenia. The quality of the assay and its preliminary clinical application have been evaluated.

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抗achr抗体的间接猝灭荧光受体测定。
采用抗荧光素血清和荧光素标记的乙酰胆碱受体(AChR),建立了一种荧光受体测定法(FRA),用于测定抗乙酰胆碱受体(AChR)抗体。兔大鼠肌AChR抗血清和标记的AChR与抗荧光素血清室温孵育。在高水平的抗AChR下,标记的AChR的结合阻止了抗荧光素随后与荧光素基团的结合,导致标记的信号几乎没有变化。相反,在低水平的抗AChR时,标记的AChR的自由部分可被抗荧光素结合,这显着降低了标记的荧光强度。因此,检测混合物的荧光强度直接反映血清中抗achr抗体的数量。由此得出结论,荧光素标记的AChR和针对它的抗体的可用性允许测定人肌无力的抗AChR抗体。对该方法的质量及其初步临床应用进行了评价。
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