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在一名因子 XI 缺乏症患者中鉴定出一种有缺陷的因子 XI 交叉反应物质。

Identification of a defective factor XI cross-reacting material in a factor XI-deficient patient.

作者信息

Mannhalter C, Hellstern P, Deutsch E

出版信息

Blood. 1987 Jul;70(1):31-7.

PMID:2439152
Abstract

A homozygous factor XI-deficient girl, who appeared to be positive for cross-reacting material (CRM+) was studied for clarification. Factor XI antigen (F XI:Ag) was measured by radial immunodiffusion using monospecific, heterologous anti-factor XI antibodies. Factor XI coagulant activity (F XI:C) was determined in a modified activated partial thromboplastin time (APTT) test. The ratio of F XI:C to F XI:Ag was 0.04 for the proposita, as compared with 0.7 to 0.74 in the other family members. In contrast, 12 normal individuals had ratios of F XI:C to F XI:Ag of 1.04 +/- 0.15. F XI esterolytic activity was clearly higher than F XI:C in the proband, but not in her relatives. Immunoblotting studies demonstrated F XI CRM in the patient's plasma. Chromatography on diethylaminoethanol (DEAE)-Sephadex at pH 8.4 led to an almost complete removal of F XI from the plasma. The defective F XI was not bound to a negatively charged kaolin surface due to an abnormal interaction with high-mol-wt kininogen (HMWK).

摘要

对一名纯合子因子 XI 缺乏的女孩进行了研究以明确情况,该女孩的交叉反应物质似乎呈阳性(CRM+)。使用单特异性、异源抗因子 XI 抗体通过放射免疫扩散法测定因子 XI 抗原(F XI:Ag)。在改良的活化部分凝血活酶时间(APTT)试验中测定因子 XI 凝血活性(F XI:C)。先证者的 F XI:C 与 F XI:Ag 的比值为 0.04,而其他家庭成员的该比值为 0.7 至 0.74。相比之下,12 名正常个体的 F XI:C 与 F XI:Ag 的比值为 1.04±0.15。先证者的 F XI 酯解活性明显高于 F XI:C,但其亲属并非如此。免疫印迹研究在患者血浆中证实了 F XI CRM。在 pH 8.4 条件下于二乙氨基乙醇(DEAE)-葡聚糖凝胶上进行层析,几乎可使血浆中的 F XI 完全去除。由于与高分子量激肽原(HMWK)存在异常相互作用,缺陷型 F XI 未与带负电荷的高岭土表面结合。

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