Aquaporin-4 antibodies in patients treated with natalizumab for suspected MS

Anna Gahlen; Anne-Kathrin Trampe; Steffen Haupeltshofer; Marius Ringelstein; Orhan Aktas; Achim Berthele; Brigitte Wildemann; Ralf Gold; Sven Jarius; Ingo Kleiter

doi:10.1212/NXI.0000000000000363

Aquaporin-4 antibodies in patients treated with natalizumab for suspected MS

Neurol Neuroimmunol Neuroinflamm. 2017 Jun 16;4(4):e363. doi: 10.1212/NXI.0000000000000363. eCollection 2017 Jul.

Affiliation

¹ Department of Neurology (A.G., A.-K.T., S.H., R.G., I.K.), St. Josef-Hospital, Ruhr-University Bochum; Department of Neurology (M.R., O.A.), Medical Faculty, Heinrich-Heine-University Düsseldorf; Department of Neurology (A.B.), Klinikum Rechts der Isar, Technische Universität München; and Molecular Neuroimmunology Group (B.W., S.J.), Department of Neurology, University of Heidelberg, Germany.

Abstract

Objective: To evaluate (1) the frequency of aquaporin-4 antibody (AQP4-ab)-seropositive cases among patients treated with natalizumab (NAT) and previously diagnosed with MS (MS^NAT) in a nationwide cohort, (2) the clinical course of NAT-treated AQP4-ab-seropositive neuromyelitis optica spectrum disorder (NMOSD) patients (NMO^NAT), (3) AQP4-ab titers in NMO^NAT and AQP4-ab-seropositive NMOSD treated with other immunotherapies (NMO^IT), and (4) immune mechanisms influencing disease activity in NMO^NAT.

Methods: MS^NAT serum samples were retrospectively screened with a cell-based assay for AQP4-IgG and titers determined by ELISA. The annualized relapse rate (ARR) and disability progression were assessed. Serum levels of proinflammatory cytokines (interleukin [IL]-1β, IL-4, IL-6, IL-8, IL-10, IL-17, IL-21, and interferon [IFN]-γ) and the chemokine CXCL-10 of NMO^NAT patients identified in this (n = 4) and a previous study (n = 5) were measured by cytometric bead array and ELISA.

Results: Of the 1,183 MS^NAT patients (851 female, median 9 NAT infusions), only 4 (0.33%; 3 female, 1 male) had AQP4-IgG. Of these, 2 fulfilled the 2006 NMO criteria and all met the 2015 NMOSD criteria. The ARR was higher in NMO^NAT vs MS^NAT (p = 0.0182). All 4 NMO^NAT patients had relapses and 2 had an increase of disability. AQP4-ab titers were higher in NMO^NAT (n = 9) vs NMO^IT (n = 13; p = 0.0059). IL-8, IL-1β, and IFN-γ serum levels were significantly higher, and CXCL-10 was significantly lower in NMO^NAT vs NMO^IT.

Conclusions: Misdiagnosis of NMOSD with MS is rare. NAT was not able to control disease activity in NMO^NAT patients, who had higher serum levels of AQP4-IgG and proinflammatory cytokines than patients with NMOSD treated with other immunotherapies.