共 50 条
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.
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页码:1115 / 1122
页数:8
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