Tanaka Haruyuki, Sakai Kazuya, Tamura Shusuke, Shiwaku Hiroya, Nakamura Junko, Ueda Yasunori, Bamba Seiya, Nishikubo Masashi, Nagai Yuya, Matsumoto Masanori
Department of Hematology, Nara Medical University, Kashihara, Nara, Japan.
Department of Blood Transfusion Medicine, Nara Medical University, Kashihara, Nara, Japan.
Ann Hematol. 2025 Mar;104(3):1507-1514. doi: 10.1007/s00277-025-06318-w. Epub 2025 Mar 19.
Immune-mediated thrombotic thrombocytopenic purpura (iTTP) is a rare but life-threatening disorder characterized by severe thrombocytopenia, hemolytic anemia, and end-organ ischemic damage. The introduction of caplacizumab, an anti-von Willebrand factor A1 nanobody, has revolutionized the treatment of patients with iTTP by preventing fatal thrombotic events and shortening the time to platelet normalization. Despite its benefits, caplacizumab does not address the challenge of anti-ADAMTS13 autoantibody production, posing a risk of ADAMTS13 inhibitor boosting and delayed recovery of ADAMTS13 activity. Here, we highlight three challenging cases from the Japanese TTP registry involving patients with iTTP who experienced severe ADAMTS13 inhibitor boosting. This delayed the recovery of ADAMTS13, and extended administration of caplacizumab while requiring additional therapeutic plasma exchange (TPE) and immunosuppressive therapy. All patients demonstrated delayed recovery of ADAMTS13 activity despite initial clinical improvement. Prolonged use of caplacizumab masked the persistence of ADAMTS13 inhibitors, emphasizing the need for close monitoring and timely interventions. Although recent proposals for TPE-free regimens show promise, our findings underscore that TPE remains essential for removing residual autoantibodies and preventing disease exacerbation in certain patients. Stratifying patients based on initial ADAMTS13 inhibitor titers and optimizing immunosuppressive strategies may help identify those at risk of severe inhibitor boosting. Further research is required to refine treatment protocols and ensure the safe withdrawal of caplacizumab while achieving sustained recovery of ADAMTS13 activity.
免疫介导的血栓性血小板减少性紫癜(iTTP)是一种罕见但危及生命的疾病,其特征为严重血小板减少、溶血性贫血和终末器官缺血性损伤。抗血管性血友病因子A1纳米抗体卡泊珠单抗的引入,通过预防致命性血栓事件和缩短血小板恢复正常的时间,彻底改变了iTTP患者的治疗方式。尽管卡泊珠单抗有诸多益处,但它并未解决抗ADAMTS13自身抗体产生的问题,存在ADAMTS13抑制剂增强和ADAMTS13活性恢复延迟的风险。在此,我们重点介绍日本TTP登记处的三例具有挑战性的病例,这些病例涉及经历严重ADAMTS13抑制剂增强的iTTP患者。这延迟了ADAMTS13的恢复,延长了卡泊珠单抗的给药时间,同时需要额外的治疗性血浆置换(TPE)和免疫抑制治疗。尽管最初临床症状有所改善,但所有患者的ADAMTS13活性恢复均延迟。长期使用卡泊珠单抗掩盖了ADAMTS13抑制剂的持续存在,强调了密切监测和及时干预的必要性。尽管最近关于无TPE方案的提议显示出前景,但我们的研究结果强调,TPE对于清除残留自身抗体和预防某些患者疾病恶化仍然至关重要。根据初始ADAMTS13抑制剂滴度对患者进行分层并优化免疫抑制策略,可能有助于识别有严重抑制剂增强风险的患者。需要进一步研究以完善治疗方案,并确保在实现ADAMTS13活性持续恢复的同时安全停用卡泊珠单抗。