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阿仑单抗治疗多发性硬化症导致 B 细胞耗竭治疗后严重自身免疫并发症持续缓解。

B cell depletion therapy resulting in sustained remission of severe autoimmune complications following Alemtuzumab treatment of Multiple Sclerosis.

机构信息

Department of Neurology, St Vincent's Hospital, Sydney, NSW, Australia; St Vincent's Clinical School, University of New South Wales, Sydney, NSW, Australia.

St Vincent's Clinical School, University of New South Wales, Sydney, NSW, Australia; Department of Radiology, St Vincent's Hospital, Sydney, NSW, Australia.

出版信息

Mult Scler Relat Disord. 2019 Oct;35:100-103. doi: 10.1016/j.msard.2019.07.016. Epub 2019 Jul 20.

DOI:10.1016/j.msard.2019.07.016
PMID:31357122
Abstract

Secondary autoimmune disorders (AID) are a recognised complication of alemtuzumab treatment for multiple sclerosis. We have previously reported two female multiple sclerosis patients treated with alemtuzumab who developed rare but severe secondary AID; acquired haemophilia A and autoimmune encephalitis with seizures. Both cases proved to be refractory to treatment with conventional immuno-therapy. However, treatment of the patients with anti-CD20 therapy resulted in sustained remission. This observation validates anti-CD20 therapy as a potential treatment option in patients with autoimmune complications of alemtuzumab that are postulated to arise as a result of B cell hyperpopulation.

摘要

继发自身免疫性疾病(AID)是阿仑单抗治疗多发性硬化症的已知并发症。我们之前曾报道过两名接受阿仑单抗治疗的多发性硬化症女性患者,她们出现了罕见但严重的继发 AID;获得性血友病 A 和伴有癫痫发作的自身免疫性脑炎。这两种情况均被证明对常规免疫治疗无反应。然而,用抗 CD20 治疗对患者进行治疗导致持续缓解。这一观察结果证实了抗 CD20 治疗作为阿仑单抗引起的自身免疫并发症患者的一种潜在治疗选择的有效性,这些并发症据推测是由于 B 细胞过度增殖引起的。

相似文献

1
B cell depletion therapy resulting in sustained remission of severe autoimmune complications following Alemtuzumab treatment of Multiple Sclerosis.阿仑单抗治疗多发性硬化症导致 B 细胞耗竭治疗后严重自身免疫并发症持续缓解。
Mult Scler Relat Disord. 2019 Oct;35:100-103. doi: 10.1016/j.msard.2019.07.016. Epub 2019 Jul 20.
2
Mitigating alemtuzumab-associated autoimmunity in MS: A "whack-a-mole" B-cell depletion strategy.减轻 MS 中阿仑单抗相关自身免疫:一种“打地鼠”的 B 细胞耗竭策略。
Neurol Neuroimmunol Neuroinflamm. 2020 Aug 7;7(6). doi: 10.1212/NXI.0000000000000868. Print 2020 Nov 5.
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Autoimmune encephalitis following alemtuzumab treatment of multiple sclerosis.多发性硬化症用阿仑单抗治疗后出现自身免疫性脑炎。
Mult Scler Relat Disord. 2019 Feb;28:31-33. doi: 10.1016/j.msard.2018.12.004. Epub 2018 Dec 3.
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Acquired haemophilia A as a secondary autoimmune disease after alemtuzumab treatment in multiple sclerosis: A case report.获得性血友病 A 作为多发性硬化症阿仑单抗治疗后的继发自身免疫性疾病:一例报告。
Mult Scler Relat Disord. 2019 Jan;27:403-405. doi: 10.1016/j.msard.2018.11.029. Epub 2018 Nov 29.
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Lymphocyte pharmacodynamics are not associated with autoimmunity or efficacy after alemtuzumab.淋巴细胞药代动力学与阿仑单抗治疗后的自身免疫或疗效无关。
Neurol Neuroimmunol Neuroinflamm. 2019 Oct 29;7(1). doi: 10.1212/NXI.0000000000000635. Print 2020 Jan.
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Acquired haemophilia A complicating alemtuzumab therapy for multiple sclerosis.获得性血友病A并发阿仑单抗治疗多发性硬化症。
BMJ Case Rep. 2017 Dec 5;2017:bcr-2017-223016. doi: 10.1136/bcr-2017-223016.
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Autoimmune thyroid disease following treatment with alemtuzumab for multiple sclerosis.多发性硬化症用阿仑单抗治疗后发生自身免疫性甲状腺疾病。
Int J Immunopathol Pharmacol. 2019 Jan-Dec;33:2058738419843690. doi: 10.1177/2058738419843690.
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Incidence, management, and outcomes of autoimmune nephropathies following alemtuzumab treatment in patients with multiple sclerosis.在多发性硬化症患者中使用阿仑单抗治疗后的自身免疫性肾病的发病率、处理方法和结局。
Mult Scler. 2019 Aug;25(9):1273-1288. doi: 10.1177/1352458519841829. Epub 2019 Apr 15.
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Marked neutropenia: Significant but rare in people with multiple sclerosis after alemtuzumab treatment.显著但罕见:阿仑单抗治疗多发性硬化症后出现中性粒细胞减少症。
Mult Scler Relat Disord. 2017 Nov;18:181-183. doi: 10.1016/j.msard.2017.09.028. Epub 2017 Sep 25.
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Life-threatening autoimmune warm hemolytic anemia following treatment for multiple sclerosis with alemtuzumab.在使用阿仑单抗治疗多发性硬化症后,发生危及生命的自身免疫性温性溶血性贫血。
Mult Scler. 2018 May;24(6):811-813. doi: 10.1177/1352458517729766. Epub 2018 Jan 23.

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