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通过加用美泊利单抗改善嗜酸性肉芽肿性多血管炎患者的慢性鼻-鼻窦炎并降低髓过氧化物酶-抗中性粒细胞胞浆抗体滴度

Improvement of Chronic Rhinosinusitis and Reduction of the Myeloperoxidase-Antineutrophil Cytoplasmic Antibody Titer in a Patient with Eosinophilic Granulomatosis with Polyangiitis by Additional Mepolizumab.

作者信息

Tamechika Shin-Ya, Isogai Shuntaro, Maeda Shinji, Naniwa Taio, Niimi Akio

机构信息

Department of Respiratory Medicine Allergy and Clinical Immunology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

Department of Rheumatology, Nagoya City East Medical Center, Nagoya, Japan.

出版信息

Case Rep Rheumatol. 2021 Mar 29;2021:5561762. doi: 10.1155/2021/5561762. eCollection 2021.

Abstract

A case of eosinophilic granulomatosis with polyangiitis (EGPA) in which chronic rhinosinusitis (CRS) was improved with a reduction in the myeloperoxidase-antineutrophil cytoplasmic antibody (MPO-ANCA) titer after the addition of mepolizumab is reported. A 55-year-old woman with EGPA receiving prednisolone 5 mg/day developed CRS with increases in the eosinophil count and the MPO-ANCA titer. Although it improved with prednisolone 15 mg/day in addition to mizoribine 150 mg/day, because azathioprine could not be taken orally due to side effects, it relapsed after prednisolone was tapered to 5 mg/day. There was no exacerbation of other vasculitis symptoms such as mononeuropathy multiplex. The patient was treated with additional mepolizumab 300 mg every 4 weeks, which resulted in the improvement of CRS and marked reductions of the eosinophil count and MPO-ANCA titer, and the reduction of prednisolone to 2 mg/day. Furthermore, even after tapering mepolizumab to 200 mg every 4 weeks, her condition remained stable without relapse of EGPA and without increases in the eosinophil count and MPO-ANCA titer. The clinical course of mepolizumab treatment in this patient suggests that the IL5-dependent inflammatory cascade is one of the factors contributing to the increase in MPO-ANCA in EGPA.

摘要

报告了1例嗜酸性肉芽肿性多血管炎(EGPA)患者,在加用美泊利单抗后,慢性鼻窦炎(CRS)得到改善,髓过氧化物酶抗中性粒细胞胞浆抗体(MPO-ANCA)滴度降低。一名55岁患有EGPA的女性,每天服用5mg泼尼松龙,出现了CRS,嗜酸性粒细胞计数和MPO-ANCA滴度升高。尽管除每天150mg咪唑立宾外,加用15mg/天泼尼松龙后病情有所改善,但由于硫唑嘌呤因副作用无法口服,在泼尼松龙减至5mg/天时病情复发。未出现多发性单神经病等其他血管炎症状加重的情况。该患者每4周额外接受300mg美泊利单抗治疗,结果CRS得到改善,嗜酸性粒细胞计数和MPO-ANCA滴度显著降低,泼尼松龙减至2mg/天。此外,即使将美泊利单抗减至每4周200mg后,她的病情仍保持稳定,EGPA未复发,嗜酸性粒细胞计数和MPO-ANCA滴度也未升高。该患者美泊利单抗治疗的临床过程表明,IL5依赖性炎症级联反应是导致EGPA中MPO-ANCA升高的因素之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75e5/8024092/2de90f6979cf/CRIRH2021-5561762.001.jpg

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