Ogiwara Kenichi, Furukawa Shoko, Shinohara Sho, Tabuchi Yuka, Arai Nobuo, Noguchi-Sasaki Mariko, Soeda Tetsuhiro, Shima Midori, Nogami Keiji
Department of Pediatrics, Nara Medical University, Kashihara, Nara, Japan.
Reagent Engineering, Sysmex Corporation, Kobe, Japan.
Haemophilia. 2023 Jan;29(1):329-335. doi: 10.1111/hae.14662. Epub 2022 Sep 22.
Emicizumab markedly shortens the activated partial thromboplastin time (aPTT), resulting in inaccurate measurements of procoagulant and anticoagulant factor activities. We have recently reported that mixtures of two different anti-idiotype monoclonal antibodies against emicizumab (anti-emicizumab-mAbs) allow measurement of factor (F)VIII activity (FVIII:C) and FVIII inhibitor in emicizumab-containing plasmas. It is unknown whether anti-emicizumab mAbs can work for other aPTT-based procoagulant and anticoagulant assays.
To investigate whether anti-emicizumab mAbs were measured by all of the aPTT-based assays tested.
Two anti-emicizumab-mAbs (300 μg/mL each) were preincubated with emicizumab (200 μg/mL)-spiked FVIII-deficient plasma; we then measured FVIII:C, FIX:C, FXI:C, FXII:C, protein (P)C:C, PS:C, global PC-FV (aPTT-based), and prothrombin time (PT), diluted Russel's viper venom time (dRVVT), chromogenic-based FVIII:C, FIX:C and PC:C (non-aPTT-based). Emicizumab (100 μg/mL)-spiked haemophilia (H)A plasmas from patients (n = 23) were also measured.
Emicizumab shortened the clotting time in all aPTT-based assays, resulting in high levels of FVIII:C, FIX:C, FXI:C and FXII:C; low levels of PC:C and PS:C; and false-positive results for activated PC resistance. The addition of anti-emicizumab-mAbs to emicizumab-added plasma restored all factors to the initial levels without emicizumab. Chromogenic FVIII:C measurement by human FIXa/FX was affected by emicizumab, but anti-emicizumab mAbs cancelled this effect. PT-based assays and dRVVT, chromogenic FIX:C and PC:C assays showed no effect with emicizumab. Twenty-three plasma samples from HA patients also showed similar patterns.
Anti-emicizumab mAbs in vitro could cancel the effect of emicizumab, irrespective of the test base, resulting in accurate measurements of procoagulant and anticoagulant factor activity.
艾美赛珠单抗可显著缩短活化部分凝血活酶时间(aPTT),导致对促凝血和抗凝血因子活性的测量不准确。我们最近报道,两种不同的抗艾美赛珠单抗独特型单克隆抗体(抗艾美赛珠单抗单克隆抗体)的混合物可用于测量含艾美赛珠单抗血浆中的因子(F)VIII活性(FVIII:C)和FVIII抑制剂。尚不清楚抗艾美赛珠单抗单克隆抗体是否可用于其他基于aPTT的促凝血和抗凝血检测。
研究抗艾美赛珠单抗单克隆抗体是否能通过所有测试的基于aPTT的检测方法进行测量。
将两种抗艾美赛珠单抗单克隆抗体(各300μg/mL)与添加了艾美赛珠单抗(200μg/mL)的FVIII缺陷血浆预孵育;然后我们测量FVIII:C、FIX:C、FXI:C、FXII:C、蛋白(P)C:C、PS:C、整体PC-FV(基于aPTT)和凝血酶原时间(PT)、稀释的罗素蝰蛇毒时间(dRVVT)、基于显色法的FVIII:C、FIX:C和PC:C(非基于aPTT)。还对来自患者(n = 23)的添加了艾美赛珠单抗(100μg/mL)的血友病(H)A血浆进行了测量。
艾美赛珠单抗缩短了所有基于aPTT的检测中的凝血时间,导致FVIII:C、FIX:C、FXI:C和FXII:C水平升高;PC:C和PS:C水平降低;以及活化PC抵抗出现假阳性结果。向添加了艾美赛珠单抗的血浆中添加抗艾美赛珠单抗单克隆抗体可使所有因子恢复到未添加艾美赛珠单抗时的初始水平。用人FIXa/FX进行的显色法FVIII:C测量受艾美赛珠单抗影响,但抗艾美赛珠单抗单克隆抗体消除了这种影响。基于PT的检测以及dRVVT、显色法FIX:C和PC:C检测显示艾美赛珠单抗无影响。来自HA患者的23份血浆样本也显示出类似模式。
体外抗艾美赛珠单抗单克隆抗体可消除艾美赛珠单抗的影响,无论检测基础如何,从而实现对促凝血和抗凝血因子活性的准确测量。