Analysis of Soluble and Humoral Immunological Parameters During Re-exposure with rFVIIIFc after History of Inhibitors.

IF 2.4 4区 医学 Q2 HEMATOLOGY
Anja Schmidt, Stephan Schultze-Strasser, Diana Stichel, Aleksander Orlowski, Christine Heller, Christoph Königs
{"title":"Analysis of Soluble and Humoral Immunological Parameters During Re-exposure with rFVIIIFc after History of Inhibitors.","authors":"Anja Schmidt, Stephan Schultze-Strasser, Diana Stichel, Aleksander Orlowski, Christine Heller, Christoph Königs","doi":"10.1055/a-2722-8734","DOIUrl":null,"url":null,"abstract":"<p><p>Little is known on the mechanisms of tolerance to factor VIII (FVIII) in haemophilia A (HA) patients. To identify immunological markers in tolerance development, samples from two patients with HA treated with rFVIIIFc after a history of inhibitors were analyzed. The patients have been followed closely during re-exposure with FVIII as part of immune tolerance induction. Plasma samples were analyzed for FVIII inhibitors and FVIII-specific antibodies. Analysis of further immunological markers was performed for patient 2 using peripheral blood mononuclear cells (PBMCs); additionally, cytokines in cell culture media were quantified. Laboratory data were compared to pharmacological parameters and clinical outcome.Both patients showed a decline in FVIII recovery (exposure day [ED] 12 for patient 1, ED 25 for patient 2). During that time patient 2 was positive for lupus anticoagulants and a low amount of FVIII-specific antibodies was detectable in ELISA. However, specificity could not be verified by competition and antibodies disappeared again after ED 25. Patient 1 developed FVIII-specific antibodies of subclass IgG4 after ED 229. Antibodies were mainly directed against the FVIII light chain. FVIII-responsive CD4<sup>+</sup> T-cells were detectable in the patient's PBMCs. Additionally, PMBCs showed an elevated production of IL-23 and TNF-α when stimulated with FVIII.A prospective analysis of the described parameters might help to identify the onset of an immune response. Even though the number of analyzed patients is low, the detailed analyses may help to further understand the development of tolerance to FVIII and to define starting points for further interventions against treatment complications through inhibitor development in HA.</p>","PeriodicalId":55074,"journal":{"name":"Hamostaseologie","volume":" ","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2026-02-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hamostaseologie","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1055/a-2722-8734","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Little is known on the mechanisms of tolerance to factor VIII (FVIII) in haemophilia A (HA) patients. To identify immunological markers in tolerance development, samples from two patients with HA treated with rFVIIIFc after a history of inhibitors were analyzed. The patients have been followed closely during re-exposure with FVIII as part of immune tolerance induction. Plasma samples were analyzed for FVIII inhibitors and FVIII-specific antibodies. Analysis of further immunological markers was performed for patient 2 using peripheral blood mononuclear cells (PBMCs); additionally, cytokines in cell culture media were quantified. Laboratory data were compared to pharmacological parameters and clinical outcome.Both patients showed a decline in FVIII recovery (exposure day [ED] 12 for patient 1, ED 25 for patient 2). During that time patient 2 was positive for lupus anticoagulants and a low amount of FVIII-specific antibodies was detectable in ELISA. However, specificity could not be verified by competition and antibodies disappeared again after ED 25. Patient 1 developed FVIII-specific antibodies of subclass IgG4 after ED 229. Antibodies were mainly directed against the FVIII light chain. FVIII-responsive CD4+ T-cells were detectable in the patient's PBMCs. Additionally, PMBCs showed an elevated production of IL-23 and TNF-α when stimulated with FVIII.A prospective analysis of the described parameters might help to identify the onset of an immune response. Even though the number of analyzed patients is low, the detailed analyses may help to further understand the development of tolerance to FVIII and to define starting points for further interventions against treatment complications through inhibitor development in HA.

抑制剂史后再暴露于rfviii - ifc时的可溶性和体液免疫参数分析。
血友病A (HA)患者对因子VIII (FVIII)的耐受性机制知之甚少。为了确定耐受性发展中的免疫标志物,对两例HA患者在抑制剂史后接受rfviii ifc治疗的样本进行了分析。作为免疫耐受诱导的一部分,在再次暴露于FVIII期间密切跟踪患者。分析血浆样本中FVIII抑制剂和FVIII特异性抗体。患者2使用外周血单个核细胞(PBMCs)进一步分析免疫标志物;另外,对细胞培养基中的细胞因子进行定量。将实验室数据与药理学参数和临床结果进行比较。两例患者均表现出FVIII恢复下降(患者1暴露日[ED] 12,患者2暴露日[ED] 25)。在此期间,患者2对狼疮抗凝血药物呈阳性,ELISA检测到少量fviii特异性抗体。但特异性无法通过竞争验证,ED 25后抗体再次消失。患者1在ED 229后产生fviii特异性IgG4亚类抗体。抗体主要针对FVIII轻链。患者外周血中检测到fviii反应性CD4+ t细胞。此外,pmbc在FVIII刺激下显示IL-23和TNF-α的产生升高。对所描述的参数进行前瞻性分析可能有助于确定免疫反应的开始。尽管分析的患者数量较少,但详细的分析可能有助于进一步了解FVIII耐受性的发展,并通过HA抑制剂的发展确定进一步干预治疗并发症的起点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Hamostaseologie
Hamostaseologie HEMATOLOGY-
CiteScore
5.50
自引率
6.20%
发文量
62
审稿时长
6-12 weeks
期刊介绍: Hämostaseologie is an interdisciplinary specialist journal on the complex topics of haemorrhages and thromboembolism and is aimed not only at haematologists, but also at a wide range of specialists from clinic and practice. The readership consequently includes both specialists for internal medicine as well as for surgical diseases.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书