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  • Frontiers Media SA  (2)
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  • Frontiers Media SA  (2)
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  • 1
    Online Resource
    Online Resource
    Frontiers Media SA ; 2023
    In:  Frontiers in Neurology Vol. 14 ( 2023-6-26)
    In: Frontiers in Neurology, Frontiers Media SA, Vol. 14 ( 2023-6-26)
    Abstract: The detection of myelin oligodendrocyte glycoprotein autoantibodies (MOG-Ab) is essential for the diagnosis of MOG-Ab-associated disease (MOGAD). The clinical implications of different epitopes recognized by MOG-Ab are largely unknown. In this study, we established an in-house cell-based immunoassay for detecting MOG-Ab epitopes and examined the clinical characteristics of patients with MOG-Ab according to their epitopes. Methods We conducted a retrospective review of patients with MOG-Ab-associated disease (MOGAD) in our single center registry, and collected serum samples from enrolled patients. Human MOG variants were generated to detect epitopes recognized by MOG-Ab. The differences in clinical characteristics according to the presence of reactivity to MOG Proline42 (P42) were evaluated. Results Fifty five patients with MOGAD were enrolled. Optic neuritis was the most common presenting syndrome. The P42 position of MOG was a major epitope of MOG-Ab. The patients with a monophasic clinical course and childhood-onset patients were only observed in the group that showed reactivity to the P42 epitope. Conclusion We developed an in-house cell-based immunoassay to analyze the epitopes of MOG-Ab. The P42 position of MOG is the primary target of MOG-Ab in Korean patients with MOGAD. Further studies are needed to determine the predictive value of MOG-Ab and its epitopes.
    Type of Medium: Online Resource
    ISSN: 1664-2295
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2023
    detail.hit.zdb_id: 2564214-5
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  • 2
    Online Resource
    Online Resource
    Frontiers Media SA ; 2021
    In:  Frontiers in Immunology Vol. 12 ( 2021-7-29)
    In: Frontiers in Immunology, Frontiers Media SA, Vol. 12 ( 2021-7-29)
    Abstract: Clear associations have been found between vitamin D deficiency and several autoimmune diseases including multiple sclerosis (MS). However, the benefits of vitamin D supplementation on disease management remain a matter of debate. Objective and Methods Patients with MS ( N =12) and neuromyelitis optica spectrum disorder (NMOSD; N =12) were enrolled along with 15 healthy controls. Changes in lymphocyte subset proportions during stimulation of their peripheral blood mononuclear cells (PBMCs) with the active form of vitamin D, 1,25-dihydroxyvitamin D 3 (1,25(OH) 2 D 3 ), and correlations with serum concentrations of the vitamin D precursor 25-hydroxyvitamin D 3 (serum 25(OH)D 3 ) were explored. The impact of 1,25(OH) 2 D 3 stimulation on the expression of vitamin-D-responsive genes in immune cells was also investigated. Results In both MS and NMOSD, stimulation of PBMCs with 1,25(OH) 2 D 3 followed by steroid suppressed the proliferation of total lymphocytes and T cells. The ratio of CD19 + CD27 + memory B cells (Bmem) to all B cells after stimulation with 1,25(OH) 2 D 3 was negatively correlated with serum 25(OH)D 3 in MS (Spearman’s ρ =–0.594, p =0.042), but positively correlated in NMOSD (Pearson’s r = 0.739, p =0.006). However, there was no relationship between the ratio of Bmem to CD19 + CD24 + CD38 + regulatory B cells and serum 25(OH)D 3 in either MS or NMOSD. In addition, the level of 1,25(OH) 2 D 3 -induced CYP24A1 mRNA expression in PBMCs was significantly and negatively correlated with serum 25(OH)D 3 (for ΔC T , r =0.744, p =0.014) in MS. Conclusion These findings suggest a beneficial impact of stimulation of PBMCs with vitamin D followed by steroid on the T-cell population. The association between patient serum 25(OH)D 3 and the proportion of Bmem under immune-cell stimulation differed between MS and NMOSD. Further investigations are warranted with larger patient populations.
    Type of Medium: Online Resource
    ISSN: 1664-3224
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2021
    detail.hit.zdb_id: 2606827-8
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