NeuroImmunoModulation · 2013 · 31 citations · 22 references
Life SciencesImmunologyNeurologyAutoimmunityInflammationNeuroimmunologyCerebrospinal Fluid BiomarkersCerebrospinal Fluid ImmunologyCytokine BiologyCytokine-mediated PathologyMultiple SclerosisNeuroinflammationCentral Nervous System CytokinesCerebrospinal Fluid CytokinesDisease Activity MeasurementHigh-mobility Group Box 1 ProteinHigh-mobility Group Box 1 ReleaseHigh-mobility Group Box 1 SignalingNeuroinflammatory MarkersNeuroinflammatory Mediators
<b><i>Background:</i></b> Neuromyelitis optica (NMO) and multiple sclerosis (MS) are two autoimmune inflammatory demyelinating diseases in the central nervous system. Interleukin (IL)-6 and IL-17 may play important roles in the pathogenesis of these diseases. High-mobility group box protein 1 (HMGB1) can activate the nuclear factor <!-- NICHT DEFINIERT -Kleines Kapitaelchen K --> light chain enhancer of activated B cells and release cytokines such as IL-6 and IL-17. However, whether cerebrospinal fluid (CSF) HMGB1 levels were altered in NMO and MS patients is still unclear. <b><i>Objectives:</i></b> It was our aim to measure the CSF HMGB1 concentration in NMO patients and explore their relationship with IL-6, IL-17 and disease activity. <b><i>Methods:</i></b> CSF HMGB1 was measured by enzyme-linked immunosorbent assay in NMO (n = 22) and MS (n = 18) patients as well as in controls (n = 14). <b><i>Results:</i></b> CSF HMGB1 was notably higher in the NMO group compared with controls (p = 0.007). CSF HMGB1 positively correlated with IL-6 and IL-17 in NMO patients (IL-6, p = 0.034; IL-17, p < 0.001). <b><i>Conclusions:</i></b> In conclusion, our study suggests that CSF levels of HMGB1 are increased in patients with NMO and reflect the neuroinflammatory process.
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