In:
Neurology - Neuroimmunology Neuroinflammation, Ovid Technologies (Wolters Kluwer Health), Vol. 4, No. 4 ( 2017-07), p. e363-
Kurzfassung:
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.
Materialart:
Online-Ressource
ISSN:
2332-7812
DOI:
10.1212/NXI.0000000000000363
Sprache:
Englisch
Verlag:
Ovid Technologies (Wolters Kluwer Health)
Publikationsdatum:
2017
ZDB Id:
2767740-0
