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Eur J Neurol. 2015 Dec;22(12):1511-8, e82-3. doi: 10.1111/ene.12679. Epub 2015 Feb 16.

Neuromyelitis optica: a positive appraisal of seronegative cases.

Author information

1
INSERM U1043, CNRS, UMR 5282, Centre de Physiopathologie de Toulouse Purpan, Toulouse, France.
2
Service de Neurologie A, Observatoire Français de la Sclérose en Plaques, EDMUS Coordinating Center and Eugène Devic EDMUS Foundation against Multiple Sclerosis, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, Bron, France.
3
Team ONCOFLAM, INSERM U1028, CNRS, UMR 5292, Center for Research in Neuroscience of Lyon, Lyon, France.

Abstract

Neuromyelitis optica (NMO) is a rare inflammatory disorder of the central nervous system. The hallmark of NMO is the presence of specific autoantibodies directed against aquaporin 4 (AQP4-IgG). AQP4-IgG, included in diagnostic criteria, has enlarged the clinical spectrum of NMO and serves to predict relapses. Moreover AQP4-IgG has provided unprecedented insight in the immunopathology of NMO, representing a rationale for therapeutic intervention with relevant novel treatment strategies specific for NMO. However, some patients remain seronegative for AQP4-IgG despite a definite diagnosis of NMO and the use of the finest methods for antibody detection. Interestingly, seronegative NMO (NMO(neg)) patients exhibit different demographic and disease-related characteristics in comparison to seropositive patients. The recent association with autoantibodies specific for myelin oligodendrocyte glycoprotein (MOG) is the main indication that disease mechanisms might differ in NMO(pos) and NMO(neg), challenging the position of NMO(neg) patients in the spectrum of demyelinating diseases and therapeutic strategies to be adopted. Thus, a reappraisal of the NMO(neg) population is needed to improve NMO care. Here the current knowledge regarding NMO(neg) is reviewed and hypotheses on its pathogenesis are made including a comprehensive description of detection methods and the prevalence of AQP4-IgG and a review of the epidemiological, clinical and paraclinical characteristics of NMO(neg); finally an integrated view of the general pathophysiological mechanisms underlying NMO(neg) is provided.

KEYWORDS:

autoantibodies; autoimmune diseases; demyelinating diseases; neuromyelitis optica; optic neuritis; transverse myelitis

PMID:
25689634
DOI:
10.1111/ene.12679
[Indexed for MEDLINE]

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