Neuromyelitis optica and pregnancy during therapeutic B cell depletion: infant exposure to anti-AQP4 antibody and prevention of rebound relapses with low-dose rituximab postpartum

Author:

Ringelstein M1,Harmel J1,Distelmaier F2,Ingwersen J1,Menge T1,Hellwig K3,Kieseier B1,Mayatepek E2,Hartung H-P1,Kuempfel T4,Aktas O1

Affiliation:

1. Department of Neurology, Medical Faculty, Heinrich-Heine-University Düsseldorf, Germany

2. Department of General Pediatrics, Neonatology and Pediatric Cardiology, University Children’s Hospital, Medical Faculty, Heinrich-Heine-University Düsseldorf, Germany

3. Department of Neurology, St. Josef-Hospital, Ruhr University Bochum, Germany

4. Institute of Clinical Neuroimmunology, Ludwig-Maximilians-University Munich, Germany

Abstract

Neuromyelitis optica (NMO) predominantly affects women, some in childbearing age, and requires early therapeutic intervention to prevent disabling relapses. We report an anti-AQP4 antibody-seropositive patient who became pregnant seven months after low-dose (100 mg) rituximab application. Pregnancy showed no complications, and low-dose rituximab restarted two days after delivery resulted in neurological stability for 24 months. Remarkably, her otherwise healthy newborn presented with anti-AQP4 antibody and reduced B lymphocyte counts in umbilical cord blood, which normalized three months later. Confirming and extending previous reports, our case suggests that low-dose rituximab might be compatible with pregnancy and prevent rebound NMO disease activity postpartum.

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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