MEPOLIZUMAB FOR CHURG-STRAUSS SYNDROME

被引:0
|
作者
Antoniu, S. A. [1 ]
机构
[1] Univ Med & Pharm, Iasi, Romania
关键词
Churg-Strauus syndrome; Eosinophilic esophagitis; Polyangitis; Immunosuppressor; Mepolizumab; EOSINOPHILIC GRANULOMATOSIS; POLYARTERITIS-NODOSA; MONOCLONAL-ANTIBODY; INTERLEUKIN-5; ASTHMA; POLYANGIITIS; IL-5; PHARMACOKINETICS; ACTIVATION; APOPTOSIS;
D O I
10.1358/dof.2014.039.04.2116667
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The Churg-Strauss syndrome (eosinophilic granulomatosis with polyangiitis) is a rare systemic disease which can manifest with asthma, neuritis, renal impairment or fibrosing myocarditis, the latter two features being associated with a significant life-threatening potential. In this disease, conventional therapy represented by systemic cortico steroids or other immunosuppressor agents is usually associated with a variable therapeutic response, and therefore other approaches should be considered. One such approach is represented by the inhibition of a specific pathway resulting in upregulated eosinophilic inflammation. A relevant example in this respect is mepolizumab, a monoclonal anti-IL-5 antibody initially investigated for asthma and currently also evaluated for Churg-Strauss syndrome and eosinophilic esophagitis. In Churg-Strauss syndrome, mepolizumab would have the advantage of inhibiting eosinophilic inflammation at the systemic level, and in fact, in the few existing clinical studies it was found to induce a sustained eosinophil depletion. However, the long-term efficacy and safety should be further documented.
引用
收藏
页码:269 / 274
页数:6
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