Interferon Alpha Association with Neuromyelitis Optica

Nasrin Asgari,Kirsten Ohm Kyvik,Egon Stenager,Troels Steenstrup,Soeren Thue Lillevang,Anne Voss

doi:10.1155/2013/713519

Abstract

Interferon-alpha (IFN-α) has immunoregulatory functions in autoimmune inflammatory diseases. The goal of this study was to determine occurrence and clinical consequences of IFN-α in neuromyelitis optica (NMO) patients. Thirty-six NMO and 41 multiple sclerosis (MS) patients from a population-based retrospective case series were included. Expanded Disability Status Scale (EDSS) score and MRI findings determined disease activity. Linear regression was used to assess the effects of the level of IFN-α on disability (EDSS). IFN-α was determined by sensitive ELISA assays. IFN-α was detectable in sera from 9/36 NMO patients, significantly more often than in the MS group (2/41) (P = 0.0197). A higher frequency of IFN-α was observed in NMO patients with acute relapse compared to NMO patients in remission (P < 0.001) and compared to the MS patients with relapse (P = 0.010). In NMO patients, the levels of IFN-α were significantly associated with EDSS (P = 0.0062). It may be concluded that IFN-α was detectable in a subgroup of NMO patients. Association of IFN-α levels with clinical disease activity and severity suggests a role for IFN-α in disease perpetuation and may provide a plausible explanation for a negative effect of IFN-1 treatment in NMO patients.

Highlights

Inflammation in the central nervous system (CNS) is a decisive feature of multiple sclerosis (MS) and neuromyelitis optica (NMO) [1, 2]
MS seems to be induced by T-cellmediated attacks on the myelin, whereas NMO involves antibodies directed against the water channel aquaporin-4 (AQP4), which is highly expressed in astrocytes in the CNS [1, 3]
IFN-α was detected in sera from 9/36 NMO patients (5 anti-AQP4 antibody positive), significantly more than 2/41 MS patients (2/41) (odds ratio (OR) = 6.5; 95% confidence interval (CI) (1.18–64.96, P = 0.02)) (Figure 1)

Summary

Introduction

Inflammation in the central nervous system (CNS) is a decisive feature of multiple sclerosis (MS) and neuromyelitis optica (NMO) [1, 2]. MS seems to be induced by T-cellmediated attacks on the myelin, whereas NMO involves antibodies directed against the water channel aquaporin-4 (AQP4), which is highly expressed in astrocytes in the CNS [1, 3]. The exact importance of IFNs in NMO disease pathogenesis has not yet been elucidated. The therapeutic action of IFN-β in MS reduces relapses and delays disability progression involving numerous mechanisms [7]. In conformity with this observation, mice deficient in IFN1 receptor (IFNAR) signaling develop more severe experimental autoimmune encephalomyelitis (EAE) as a model for Clinical and Developmental Immunology

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