14 research outputs found

    Anti‐GM<sub>1</sub> IgG antibodies and <i>campylobacter </i>bacteria in Guillain‐BarrĂ© syndrome:Evidence of molecular mimicry

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    In Guillain‐BarrĂ© syndrome antibodies to GM1 and the presence of an antecedent Campylobacter jeJunei infection are correlated with a more severe course of the disease. From a group of 137 consecutive GBS patients, 11 sera had elevated titers of anti‐GM1 IgG antibodies during the acute stage of disease. Each serum sample was preincubated with three different Penner serotypes of whole C. jeJunei (PEN O:4/59, PEN O:41) and Campylobacter coli (PEN O:22) bacteria. The PEN O:4/59 serotype, isolated from the stools of a Guillain‐BarrĂ© syndrome patient, inhibited 63 to 93% of the anti‐GM1 activity in 6 of 11 patients. The PEN O:41 inhibited 63 to 100% of the anti‐GM1 antibody activity in 9 of 11 patients. The PEN O:22 inhibited anti‐GM1 antibody activity in only 2 of 11 patients (80 and 86%). Two Guillain‐BarrĂ© syndrome patients did not show antibody absorption by any of the Campylobacter serotypes tested, although this does not exclude the involvement of other serotypes. An Escherichia coli control strain did not significantly absorb anti‐GM1 antibodies. The results of this study indicate that anti‐GM1 IgG antibodies in Guillain‐BarrĂ© syndrome sera recognize surface epitopes on whole Campylobacter bacteria and that this recognition is strain‐specific. This provides evidence for molecular mimicry in the pathogenesis of Guillain‐BarrĂ© syndrome.</p

    EnergAR:exploring the energy transition at home

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    Anti‐GM<sub>1</sub> IgG antibodies and <i>campylobacter </i>bacteria in Guillain‐BarrĂ© syndrome:Evidence of molecular mimicry

    Get PDF
    In Guillain‐BarrĂ© syndrome antibodies to GM1 and the presence of an antecedent Campylobacter jeJunei infection are correlated with a more severe course of the disease. From a group of 137 consecutive GBS patients, 11 sera had elevated titers of anti‐GM1 IgG antibodies during the acute stage of disease. Each serum sample was preincubated with three different Penner serotypes of whole C. jeJunei (PEN O:4/59, PEN O:41) and Campylobacter coli (PEN O:22) bacteria. The PEN O:4/59 serotype, isolated from the stools of a Guillain‐BarrĂ© syndrome patient, inhibited 63 to 93% of the anti‐GM1 activity in 6 of 11 patients. The PEN O:41 inhibited 63 to 100% of the anti‐GM1 antibody activity in 9 of 11 patients. The PEN O:22 inhibited anti‐GM1 antibody activity in only 2 of 11 patients (80 and 86%). Two Guillain‐BarrĂ© syndrome patients did not show antibody absorption by any of the Campylobacter serotypes tested, although this does not exclude the involvement of other serotypes. An Escherichia coli control strain did not significantly absorb anti‐GM1 antibodies. The results of this study indicate that anti‐GM1 IgG antibodies in Guillain‐BarrĂ© syndrome sera recognize surface epitopes on whole Campylobacter bacteria and that this recognition is strain‐specific. This provides evidence for molecular mimicry in the pathogenesis of Guillain‐BarrĂ© syndrome.</p

    Ileum resection is the most predictive factor for osteoporosis in patients with Crohn's disease

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    INTRODUCTION: Crohn's disease is associated with a host of factors potentially increasing the risk for osteoporosis and fractures. The aim of our study was to identify the most predictive factors for skeletal pathology in this patients. METHODS: Using a cross-sectional study design, 146 randomly selected patients with Crohn's disease of variable disease activity who were given standard therapy to control disease activity, including glucocorticoids, and who attended the outpatient clinic of the Gastroenterology Unit on regular follow-up visits were studied. Bone mineral density (BMD) measurements and lateral X-rays of the spine were performed, and biochemical parameters of bone turnover, gonadal hormones and C-reactive protein (CRP) as markers of disease activity were measured in all patients. RESULTS: There were 61 men and 85 women, with a mean age of 43 years and mean disease duration of 20 years. The majority of patients (86%) had been treated with glucocorticoids at some stage during their illness at a median dose of 7.5 mg/day, 43% were currently using these agents and 66% had undergone an intestinal resection. Twenty-one percent of patients had below-normal 25-hydroxy vitamin D levels. Osteoporosis was documented in 26% of patients, predominantly at the femoral neck, but also at the lumbar spine or at both sites; osteopenia was documented in 45% of patients. Prevalence of vertebral and non-vertebral fractures was, respectively, 6% and 12%. Ileum resection was the most predictive factor for osteoporosis: RR 3.84 (CI 1.24-9.77, p=0.018), followed by age: RR 1.05 (CI 1.02-1.08, p <0.001) and current or past glucocorticoid use: RR 1.94 (CI 0.92-4.10, p=0.08). CONCLUSION: Our data suggest that in patients with Crohn's disease, the risk of osteoporosis is best predicted by a history of ileum resectio
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