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在一名多发性硬化症患者的脑脊液和血清中鉴定出一种独特的个体基因型。

Identification of a unique idiotype in cerebrospinal fluid and serum of a patient with multiple sclerosis.

作者信息

Baird L G, Tachovsky T G, Sandberg-Wollheim M, Koprowski H, Nisonoff A

出版信息

J Immunol. 1980 May;124(5):2324-8.

PMID:6154100
Abstract

Anti-idiotypic antibodies were prepared in mouse ascites fluid against the CSF-IgG of a patient with multiple sclerosis. After adsorption with pooled human IgG, the ascites fluid antibodies precipitated 20% of labeled autologous CSF IgG. By using a competitive radioimmunoassay, less than one microgram of unlabeled CSF IgG produced 50% inhibition of binding autologous 125I-labeled CSF IgG, whereas 50 micrograms of normal HIgG was not inhibitory. The idiotype could be found in both serum and CSF IgG and persisted over a 5-year period. The absolute concentration of idiotype in the CSF varied somewhat but remained from 4 to 10 times greater than that of the serum. One of 14 heterologous MS CSF was found to contain small amounts of inhibitory protein; eight CSF from patients with other neurologic diseases did not contain the idiotype.

摘要

以一名多发性硬化症患者的脑脊液免疫球蛋白(CSF-IgG)为抗原,在小鼠腹水中制备了抗独特型抗体。用混合人免疫球蛋白吸附后,腹水抗体沉淀了20%的标记自体脑脊液免疫球蛋白。通过竞争性放射免疫测定法,不到1微克的未标记脑脊液免疫球蛋白可产生50%的自体125I标记脑脊液免疫球蛋白结合抑制,而50微克的正常人类免疫球蛋白则无抑制作用。独特型可在血清和脑脊液免疫球蛋白中发现,并持续存在5年。脑脊液中独特型的绝对浓度有所变化,但仍比血清中的高4至10倍。14份异源性多发性硬化症脑脊液中有1份含有少量抑制性蛋白;8份其他神经系统疾病患者的脑脊液中未含有独特型。

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