14 research outputs found

    O brendiranju ĆŸigova i pečata

    Get PDF
    MBP staining of murine organotypic brain slices shows myelin health status of all MOG-positive samples (MOG 1-10) and MOG-negative control (Ctrl 1) as well as healthy control sample (HC 1) in combination with human complement. (DOCX 6029 kb

    time to cognitive dysfunction.

    No full text
    <p>Kaplan-Meier curves of the risk of developing cognitive dysfunction according to disability status 10 years after onset. Log rank test used for calculation of significancy.</p

    Percentages of CD3+ T cells (A), CD19+CD138− mature B cells (B) and CD19+CD138+ plasma blasts (C) in the CSF of patients with a CIS, RRMS, CPMS and OND.

    No full text
    <p>Individual data points are shown as circles and horizontal bars indicate means. Data were compared using the Kruskal-Wallis test and Dunn's multiple comparison post-hoc test and overall p-values are shown in each figure. # = significant differences to the OND group.</p

    Correlation of CSF B cells with other inflammatory parameters.

    No full text
    <p><b>1</b> data are shown as median (range), p-value: groups were compared using <b>2</b> Mann-Whitney U test or <b>3</b> Spearmans nonparametric correlations.</p><p>Abbreviations: MRI Gd+ lesions = presence of gadolinium-enhancing lesions on T1-weighted MRI (neg = negative, pos = positive), MRI T2 lesions = number of lesions on T2-weighted MRI, Q-Alb = albumin quotient, OCB = oligoclonal bands, MMP = matrix metalloproteinase, R = Spearman's correlation coefficient, ns = statistically not significant.</p

    CSF B cell subsets.

    No full text
    <p>(A) Dot plots of CSF leucocytes according to their CD45-PerCP versus side scatter properties (left panel) and forward versus side scatter properties (right panel). Region 1 (R1, left panel) was used for acquisition of a minimum number of 1000 events and region 2 (R2, right panel) was used for analysis. CSF analysis of representative patients with a CIS (B), RRMS (C), CPMS (D) and OND (E) for the presence of CD3+ T cells and CD19+ B cells (left panel), and CD19+CD138− mature B cells, CD19+CD138+ plasma blasts and CD19−CD138+ plasma cells (right panel). The numbers represent the relative percentages of these cell populations.</p

    Demographic, clinical and CSF data of analyzed patients.

    No full text
    <p><b>1</b> data are shown as median (range), p-value: groups were compared using <b>2</b> Qui-Square test or <b>3</b> Kruskal-Wallis test and Dunn's multiple comparison post-hoc test, # statistically significant different from OND control group.</p><p>Abbreviations: n = number of patients, y = years, EDSS = expanded disability status score, acute relapse = number of patients with an acute relapse, MRI Gd+ lesions = presence of gadolinium-enhancing lesions on T1-weighted MRI (neg = negative, pos = positive), ≄9 T2 MRI lesions = ≄9 lesions on T2-weighted MRI, OCB = oligoclonal bands, Q-Alb = albumin quotient, MMP = matrix metalloproteinase, ratio = CSF∶serum ratio, ns = statistically not significant.</p

    Different staining patterns of NMO-IgG in M-1 and M-23 AQP4 transfected cells.

    No full text
    <p>Anti-AQP4 IgG (red) in NMO patient's serum targets AQP4 (green), which is expressed by transiently transfected HEK cells. Performing the assay for M-23 AQP4 (<b>A</b>, green) versus M-1 AQP4 (<b>B</b>, green), results in different staining patterns of NMO-IgG (red). Weaker binding was observed to M-1 AQP4, which contrary to M-23 AQP4 forms only few orthogonal arrays of particles.</p

    M-1 and M-23 AQP4-IgG titer values in follow-up samples.

    No full text
    <p>Higher titer values of NMO-IgG in two patients with recurrent ON (1<sup>st</sup> sample) after conversion into NMO (2<sup>nd</sup> sample) after 2.6 and 8.7 years. With increasing M-23 AQP4-IgG titers, patient one developed Abs against full length AQP4, whereas patient two remained M-1 AQP4-IgG negative.</p
    corecore