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血友病 A 中重组因子 VIII-Fc(rFVIIIFc)的观察性研究。

Observational study of recombinant factor VIII-Fc, rFVIIIFc, in hemophilia A.

机构信息

University of Pittsburgh Department of Medicine and Hemophilia Center of Western PA, Pittsburgh, PA, United States of America.

University of Pittsburgh Department of Medicine and Hemophilia Center of Western PA, Pittsburgh, PA, United States of America; Chilren's Hospital of Pittsburgh, University of Pittsburgh, Pittsburgh, PA, United States of America.

出版信息

Thromb Res. 2020 Nov;195:51-54. doi: 10.1016/j.thromres.2020.07.004. Epub 2020 Jul 5.

Abstract

INTRODUCTION

rFVIIIFc (Eloctate) is an extended-half-life recombinant factor VIII-Fc fusion protein that may promote factor VIII (FVIII) tolerance through Fc immunoregulatory properties. Yet, little is known regarding its immunogenicity in patients with hemophilia A (HA) or in HA with inhibitors (HA-I), including tolerized, immune tolerance induction (ITI)-refractory, or ITI-naïve.

METHODS

We reviewed medical records of 60 patients, including 2 previously-untreated patients (PUPs) and 58 previously-treated patients (PTPs), cared for between 01/01/06 and 06/01/17, on whom anti-FVIII antibody data were available before and after initiating rFVIIIFc. Continuous data were analyzed by student's t-test, and discrete data by chi square or Fisher's exact test.

RESULTS

After initiating rFVIIIFc, one of two HA PUPs developed a low-responding (LR) inhibitor after 10 exposures, which resolved (anti-VIII<0.6 B.U.) within 8 additional exposures, while none of 41 HA PTPS developed an inhibitor. Among 19 HA-I PTPs with detectable inhibitors prior to rFVIIIFc, 5 developed an anamnestic response to rFVIIIFc, including 1 of 8 (12.5%) low-responding (LR), and 4 of 9 (44.9%) high-responding (HR), of whom 3 were ITI-naïve and 1 ITI-refractory. Inhibitors resolved in 4 HR within 2 months of continuing rFVIIIFc (median) but persisted in 1 LR at low titer. The remaining 11 HA-I PTPs, including 4 HR and seven LR, had no detectable inhibitor at the time of or after initiating rFVIIIFc.

DISCUSSION

rFVIIIFc was immunogenic in HA PUPs and in HA-I PTPs persistently ITI-naïve or ITI-refractory, with inhibitor resolution in the majority. rFVIIIFc immunogenicity appears to be similar to other FVIII products.

摘要

简介

rFVIIIFc(Eloctate)是一种延长半衰期的重组因子 VIII-Fc 融合蛋白,通过 Fc 免疫调节特性可能促进因子 VIII(FVIII)的耐受性。然而,对于血友病 A(HA)或有抑制剂的 HA(HA-I)患者,包括耐受、免疫耐受诱导(ITI)难治或 ITI-初治患者,其免疫原性知之甚少。

方法

我们回顾了 60 名患者的病历,包括 2 名未接受过治疗的患者(PUP)和 58 名接受过治疗的患者(PTP),他们在 2006 年 1 月 1 日至 2017 年 6 月 1 日之间接受了治疗,在开始使用 rFVIIIFc 之前和之后都有抗 FVIII 抗体的数据。连续数据采用学生 t 检验分析,离散数据采用卡方或 Fisher 确切检验分析。

结果

在开始使用 rFVIIIFc 后,两名 HA PUP 中的一名在 10 次暴露后产生了低反应性(LR)抑制剂,在另外 8 次暴露后(抗 VIII<0.6 B.U.)得到解决,而 41 名 HA PTPS 中没有一名产生抑制剂。在开始使用 rFVIIIFc 之前有可检测抑制剂的 19 名 HA-I PTP 中,有 5 名对 rFVIIIFc 产生了回忆反应,包括 1 名低反应性(LR)和 4 名高反应性(HR),其中 3 名是 ITI-初治,1 名是 ITI-难治。在继续使用 rFVIIIFc 2 个月内(中位数),4 名 HR 的抑制剂得到解决,但 1 名 LR 的抑制剂仍持续低滴度存在。其余 11 名 HA-I PTP,包括 4 名 HR 和 7 名 LR,在开始使用 rFVIIIFc 时或之后均未检测到抑制剂。

讨论

rFVIIIFc 在 HA PUP 和持续 ITI-初治或 ITI-难治的 HA-I PTP 中具有免疫原性,大多数患者的抑制剂得到解决。rFVIIIFc 的免疫原性似乎与其他 FVIII 产品相似。

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