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在日本的 33 名自身免疫性因子 XIII 缺乏症患者中检测因子 XIII 抑制剂。

Detection of factor XIII inhibitors in 33 patients with autoimmune factor XIII deficiency in Japan.

机构信息

Department of Molecular Patho-Biochemistry and Patho-Biology, Yamagata University School of Medicine, Yamagata, 990-9585, Japan.

The Japanese Collaborative Research Group (JCRG) On Autoimmune Acquired Coagulation Factor Deficiencies Supported By the Japanese Ministry of Health, Labor and Welfare (MHLW), Yamagata, Japan.

出版信息

Int J Hematol. 2024 Oct;120(4):472-481. doi: 10.1007/s12185-024-03807-y. Epub 2024 Jun 19.

DOI:10.1007/s12185-024-03807-y
PMID:38896335
Abstract

Autoimmune factor XIII (FXIII) deficiency (AiF13D) is a rare hemorrhagic disease. The anti-FXIII autoantibodies that cause this disease are classified into three types: type Aa inhibits the heterotetramer assembly and activation of FXIII, type Ab inhibits the enzymatic activity of activated FXIII, and type B enhances the elimination of FXIII from the blood. The former two are FXIII inhibitors and may be lethal if overlooked by conventional functional assays. To reliably detect both types of FXIII inhibitors, a new assay was developed by incorporating 5-(biotinamido)pentylamine (BAPA) into α-plasmin inhibitor (PI-BAPA assay). This assay was tested on plasma samples from 128 participants, including 60 healthy controls, 35 patients with non-immune acquired FXIII deficiency, and 33 patients with AiF13D (29 with type Aa inhibitors and 4 with type Ab inhibitors). The PI-BAPA assay successfully detected type Aa and Ab inhibitors in 5-step dilution cross-mixing tests between patient and normal plasma. This assay also showed comparable or superior inhibition rates in the 1:1 mixing test compared to conventional ammonia release and amine incorporation assays. Receiver operating characteristic curve analysis confirmed the excellent specificity and sensitivity of this assay for determining inhibition rates, and the assay has already been used for AiF13D diagnosis.

摘要

自身免疫性因子 XIII (FXIII) 缺乏症 (AiF13D) 是一种罕见的出血性疾病。导致这种疾病的抗 FXIII 自身抗体分为三类:Aa 型抑制 FXIII 异四聚体的组装和激活,Ab 型抑制活化 FXIII 的酶活性,B 型增强 FXIII 从血液中的清除。前两种是 FXIII 抑制剂,如果被常规功能检测忽视,可能是致命的。为了可靠地检测这两种类型的 FXIII 抑制剂,我们将 5-(生物素氨基)戊基胺 (BAPA) 纳入 α-纤溶酶抑制剂 (PI-BAPA 测定法),开发了一种新的检测方法。该测定法在来自 128 名参与者的血浆样本上进行了测试,包括 60 名健康对照者、35 名非免疫性获得性 FXIII 缺乏症患者和 33 名 AiF13D 患者(29 名患者存在 Aa 抑制剂,4 名患者存在 Ab 抑制剂)。PI-BAPA 测定法在患者与正常血浆的 5 步稀释交叉混合测试中成功检测到 Aa 和 Ab 抑制剂。与传统的氨释放和胺掺入测定法相比,该测定法在 1:1 混合测试中显示出可比或更高的抑制率。受试者工作特征曲线分析证实了该测定法在确定抑制率方面具有优异的特异性和敏感性,该测定法已用于 AiF13D 诊断。

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Management of autoimmune factor XIII deficiency in a frail, elderly patient.一位虚弱老年患者的自身免疫性因子 XIII 缺乏症的管理。
Blood Coagul Fibrinolysis. 2023 Sep 1;34(6):408-413. doi: 10.1097/MBC.0000000000001202. Epub 2023 Feb 7.
3
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J Thromb Haemost. 2023 Feb;21(2):255-268. doi: 10.1016/j.jtha.2022.11.019. Epub 2022 Dec 22.
4
Frequent bleeding symptoms associated with autoimmune acquired factor XIII/13 deficiency due to anti-factor XIII A and B subunit antibodies.由于抗因子XIII A和B亚基抗体导致自身免疫性获得性因子XIII/13缺乏相关的频繁出血症状。
Am J Hematol. 2022 Nov;97(11):1497-1500. doi: 10.1002/ajh.26685. Epub 2022 Aug 25.
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