Laboratory for Thrombosis Research, IRF Life Sciences, KU Leuven Campus Kulak Kortrijk, Belgium.
Service d'Hématologie Biologique, Hôpital Lariboisière, Assistance Publique-Hôpitaux de Paris, France.
Haematologica. 2019 Jun;104(6):1268-1276. doi: 10.3324/haematol.2018.205666. Epub 2018 Dec 6.
In autoantibody-mediated autoimmune diseases, autoantibody profiling allows patients to be stratified and links autoantibodies with disease severity and outcome. However, in immune-mediated thrombotic thrombocytopenic purpura (iTTP) patients, stratification according to antibody profiles and their clinical relevance has not been fully explored. We aimed to develop a new type of autoantibody profiling assay for iTTP based on the use of anti-idiotypic antibodies. Anti-idiotypic antibodies against 3 anti-spacer autoantibodies were generated in mice and were used to capture the respective anti-spacer idiotopes from 151 acute iTTP plasma samples. We next deciphered these anti-spacer idiotope profiles in iTTP patients and investigated whether these limited idiotope profiles could be linked with disease severity. We developed 3 anti-idiotypic antibodies that recognized particular idiotopes in the anti-spacer autoantibodies II-1, TTP73 or I-9, that are involved in ADAMTS13 binding; 35%, 24% and 42% of patients were positive for antibodies with the II-1, TTP73 and I-9 idiotopes, respectively. Stratifying patients according to the corresponding 8 anti-spacer idiotope profiles provided a new insight into the anti-spacer II-1, TTP73 and I-9 idiotope profiles in these patients. Finally, these limited idiotope profiles showed no association with disease severity. We successfully developed 3 anti-idiotypic antibodies that allowed us to determine the profiles of the anti-spacer II-1, TTP73 and I-9 idiotopes in iTTP patients. Increasing the number of patients and/or future development of additional anti-idiotypic antibodies against other anti-ADAMTS13 autoantibodies might allow idiotope profiles of clinical, prognostic value to be identified.
在自身抗体介导的自身免疫性疾病中,自身抗体分析可对患者进行分层,并将自身抗体与疾病严重程度和预后相关联。然而,在免疫介导的血栓性血小板减少性紫癜(iTTP)患者中,尚未充分探讨根据抗体谱及其临床相关性进行分层。我们旨在开发一种基于抗独特型抗体的新型 iTTP 自身抗体分析方法。我们在小鼠中生成了针对 3 种抗间隔区自身抗体的抗独特型抗体,并将其用于从 151 例急性 iTTP 血浆样本中捕获各自的抗间隔区独特型。接下来,我们在 iTTP 患者中破译了这些抗间隔区独特型谱,并研究了这些有限的独特型谱是否与疾病严重程度相关。我们开发了 3 种抗独特型抗体,它们分别识别参与 ADAMTS13 结合的抗间隔区自身抗体 II-1、TTP73 或 I-9 中的特定独特型;分别有 35%、24%和 42%的患者的抗体呈 II-1、TTP73 和 I-9 独特型阳性。根据相应的 8 种抗间隔区独特型谱对患者进行分层,为这些患者的抗间隔区 II-1、TTP73 和 I-9 独特型谱提供了新的认识。最后,这些有限的独特型谱与疾病严重程度无关。我们成功开发了 3 种抗独特型抗体,使我们能够确定 iTTP 患者抗间隔区 II-1、TTP73 和 I-9 独特型的谱。增加患者数量和/或未来开发针对其他抗 ADAMTS13 自身抗体的额外抗独特型抗体,可能会确定具有临床、预后价值的独特型谱。