Acute onset of autoimmune hepatitis after initiation of B cell depletion therapy in multiple sclerosis

Mara Bahri , Ankur Sheel , Austin Bolker , Wei Chen , Khalid Mumtaz , Cole A. Harrington
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Abstract

Background

Autoimmune hepatitis (AIH) is a chronic inflammatory liver disease that may coexist in the multiple sclerosis population and remain undiagnosed. AIH has previously been reported following treatment with interferon beta, glatiramer acetate, natalizumab and high dose corticosteroids in people with multiple sclerosis (MS).

Case presentation

We present a rare case of autoimmune hepatitis onset after B cell depletion with ocrelizumab in a person with multiple sclerosis (MS).

Case report

Two weeks after the second dose of ocrelizumab, patient presented with jaundice and acute liver injury. Liver biopsy revealed pathological features of autoimmune hepatitis with negative workup for viral etiologies. A six month steroid taper and azathioprine resulted in normalization of liver function tests and clinical and radiological stability of multiple sclerosis and AIH at two years of follow-up.

Conclusions

Whether B cell depletion with ocrelizumab directly resulted in emergence of AIH is unclear. Regulatory B cells have been proposed to play a protective role in AIH pathogenesis and B cell depletion may provoke the emergence of AIH through loss of regulatory B cells.

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多发性硬化症患者接受 B 细胞清除疗法后急性发作自身免疫性肝炎
背景自身免疫性肝炎(AIH)是一种慢性炎症性肝病,可能同时存在于多发性硬化症患者中,但一直未被诊断出来。病例介绍我们报告了一例罕见的自身免疫性肝炎病例,该病例是多发性硬化症(MS)患者在使用奥克立珠单抗消耗 B 细胞后发病的。病例报告在使用第二剂奥克立珠单抗两周后,患者出现黄疸和急性肝损伤。肝脏活检显示其病理特征为自身免疫性肝炎,病毒性病因检查阴性。经过六个月的类固醇减量和硫唑嘌呤治疗后,患者的肝功能检查恢复正常,随访两年后,多发性硬化和自身免疫性肝炎的临床和放射学表现稳定。有人认为调节性B细胞在AIH发病机制中起保护作用,而B细胞耗竭可能会通过调节性B细胞的丧失引发AIH的出现。
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