Secondary antibody deficiency: a complication of anti-CD20 therapy for neuroinflammation

被引:67
|
作者
Tallantyre, E. C. [1 ,2 ]
Whittam, D. H. [3 ,4 ]
Jolles, S. [1 ,2 ]
Paling, D. [5 ,6 ]
Constantinesecu, C. [7 ]
Robertson, N. P. [1 ,2 ]
Jacob, A. [3 ,4 ]
机构
[1] Univ Hosp Wales, Cardiff, S Glam, Wales
[2] Cardiff Univ, Sch Med, Cardiff, S Glam, Wales
[3] Walton Ctr NHS Trust, Liverpool L9 7LJ, Merseyside, England
[4] Univ Liverpool, Liverpool, Merseyside, England
[5] NIHR Sheffield Biomed Res Ctr Translat Neurosci, Sheffield, S Yorkshire, England
[6] Royal Hallamshire Hosp, Sheffield, S Yorkshire, England
[7] Univ Nottingham, Nottingham, England
基金
英国医学研究理事会;
关键词
Anti-CD20; Rituximab; Secondary antibody deficiency; Infection; Complication; B-CELL DEPLETION; RELAPSING MULTIPLE-SCLEROSIS; LIVED PLASMA-CELLS; NEUROMYELITIS-OPTICA; RITUXIMAB; SAFETY; OCRELIZUMAB; EFFICACY; PREDICTORS; DISEASE;
D O I
10.1007/s00415-018-8812-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
B-cell depleting anti-CD20 monoclonal antibody therapies are being increasingly used as long-term maintenance therapy for neuroinflammatory disease compared to many non-neurological diseases where they are used as remission-inducing agents. While hypogammaglobulinaemia is known to occur in over half of patients treated with medium to long-term B-cell-depleting therapy (in our cohort IgG 38, IgM 56 and IgA 18%), the risk of infections it poses seems to be under-recognised. Here, we report five cases of serious infections associated with hypogammaglobulinaemia occurring in patients receiving rituximab for neuromyelitis optica spectrum disorders. Sixty-four per cent of the whole cohort of patients studied had hypogammaglobulinemia. We discuss the implications of these cases to the wider use of anti-CD20 therapy in neuroinflammatory disease.
引用
收藏
页码:1115 / 1122
页数:8
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