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Anti-C5 as prophylactic therapy in atypical hemolytic uremic syndrome in living-related kidney transplantation.

作者信息

Pelicano Miquel Blasco, de Córdoba Santiago Rodríguez, Diekmann Fritz, Saiz Mercedes, Herrero Sara, Oppenheimer Federic, Campistol Josep M

出版信息

Transplantation. 2013 Aug 27;96(4):e26-9. doi: 10.1097/TP.0b013e31829d388d.

DOI:10.1097/TP.0b013e31829d388d
PMID:23958887
Abstract
摘要

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1
Anti-C5 as prophylactic therapy in atypical hemolytic uremic syndrome in living-related kidney transplantation.抗C5作为亲属活体肾移植中不典型溶血尿毒综合征的预防性治疗。
Transplantation. 2013 Aug 27;96(4):e26-9. doi: 10.1097/TP.0b013e31829d388d.
2
Eculizumab for atypical hemolytic-uremic syndrome.依库珠单抗用于非典型溶血性尿毒症综合征
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Tailored eculizumab therapy in the management of complement factor H-mediated atypical hemolytic uremic syndrome in an adult kidney transplant recipient: a case report.成人肾移植受者中补体因子H介导的非典型溶血性尿毒症综合征管理中的个性化依库珠单抗治疗：一例报告
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Successful 13-year ongoing remission with C5 inhibitor therapy following renal transplant in atypical hemolytic uremic syndrome.非典型溶血性尿毒症综合征肾移植后采用C5抑制剂治疗持续缓解13年
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Hemolytic Uremic Syndrome in Pregnancy and Postpartum.妊娠及产后溶血性尿毒症综合征
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Renal transplantation in patients with atypical haemolytic uraemic syndrome: a tailor made approach is necessary.非典型溶血尿毒综合征患者的肾移植：需要一种量身定制的方法。
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Prophylactic eculizumab prior to kidney transplantation for atypical hemolytic uremic syndrome.肾移植前预防性依库珠单抗治疗非典型溶血尿毒综合征。
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Prophylactic eculizumab after renal transplantation in atypical hemolytic-uremic syndrome.非典型溶血性尿毒症综合征肾移植后的预防性依库珠单抗治疗
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引用本文的文献

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The Rationale of Complement Blockade of the MCP Haplotype following Atypical Hemolytic Uremic Syndrome of Three Southeastern European Countries with a Literature Review.《三种东南欧国家非典型溶血尿毒症综合征后 MCP 单倍型补体阻断的理由：文献复习》
Int J Mol Sci. 2023 Aug 22;24(17):13041. doi: 10.3390/ijms241713041.
2
Eculizumab Use for Kidney Transplantation in Patients With a Diagnosis of Atypical Hemolytic Uremic Syndrome.依库珠单抗用于诊断为非典型溶血性尿毒症综合征患者的肾脏移植
Kidney Int Rep. 2018 Dec 3;4(3):434-446. doi: 10.1016/j.ekir.2018.11.010. eCollection 2019 Mar.
3
Complement C5-inhibiting therapy for the thrombotic microangiopathies: accumulating evidence, but not a panacea.
用于血栓性微血管病的补体C5抑制疗法：证据不断积累，但并非万灵药。
Clin Kidney J. 2017 Oct;10(5):600-624. doi: 10.1093/ckj/sfx081. Epub 2017 May 8.
4
Critical appraisal of eculizumab for atypical hemolytic uremic syndrome.依库珠单抗治疗非典型溶血性尿毒症综合征的批判性评价。
J Blood Med. 2016 Apr 12;7:39-72. doi: 10.2147/JBM.S36249. eCollection 2016.
5
Advances and challenges in the management of complement-mediated thrombotic microangiopathies.补体介导的血栓性微血管病管理中的进展与挑战
Ther Adv Hematol. 2015 Aug;6(4):171-85. doi: 10.1177/2040620715577613.
6
An international consensus approach to the management of atypical hemolytic uremic syndrome in children.儿童非典型溶血性尿毒症综合征管理的国际共识方法。
Pediatr Nephrol. 2016 Jan;31(1):15-39. doi: 10.1007/s00467-015-3076-8. Epub 2015 Apr 11.