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生成抗独特型抗体以检测急性血栓性血小板减少性紫癜患者抗间隔抗体的独特型表位。

Generation of anti-idiotypic antibodies to detect anti-spacer antibody idiotopes in acute thrombotic thrombocytopenic purpura patients.

机构信息

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.

出版信息

Haematologica. 2019 Jun;104(6):1268-1276. doi: 10.3324/haematol.2018.205666. Epub 2018 Dec 6.

DOI:10.3324/haematol.2018.205666
PMID:30523052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6545854/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae8/6545854/207f9f2ab15f/1041268.fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae8/6545854/5efcb42b8fea/1041268.fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae8/6545854/e1625e3b0a92/1041268.fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae8/6545854/2ddd1bff2298/1041268.fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae8/6545854/89a7225e3e5a/1041268.fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae8/6545854/f4f6444f98a2/1041268.fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae8/6545854/207f9f2ab15f/1041268.fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae8/6545854/5efcb42b8fea/1041268.fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae8/6545854/e1625e3b0a92/1041268.fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae8/6545854/2ddd1bff2298/1041268.fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae8/6545854/89a7225e3e5a/1041268.fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae8/6545854/f4f6444f98a2/1041268.fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ae8/6545854/207f9f2ab15f/1041268.fig6.jpg

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