4.7 Article

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

Journal

JOURNAL OF NEUROLOGY
Volume 265, Issue 5, Pages 1115-1122

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00415-018-8812-0

Keywords

Anti-CD20; Rituximab; Secondary antibody deficiency; Infection; Complication

Funding

  1. Medical Research Council [MR/L010305/1] Funding Source: Medline

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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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