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Guillain-Barré syndrome--a classical autoimmune disease triggered by infection or vaccination.

机译:格林-巴雷综合征(Guillain-Barrésyndrome)-一种经典的自身免疫性疾病,由感染或疫苗接种引发。

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Guillain-Barré syndrome (GBS) is a rare autoimmune disorder, the incidence of which is estimated to be 0.6-4/100,000 person/year worldwide. Often, GBS occurs a few days or weeks after the patient has had symptoms of a respiratory or gastrointestinal microbial infection. The disorder is sub-acute developing over the course of hours or days up to 3 to 4?weeks. About a third of all cases of Guillain-Barré syndrome are preceded by Campylobacter jejuni infection. C. jejuni strains isolated from GBS patients have a lipooligosaccharide (LOS) with a GM1-like structure. Molecular mimicry between LOS and the peripheral nerves as a cause of GBS was demonstrated in animal models of human GBS. Following the "swine flu" virus vaccine program in the USA in 1976, an increase in incidence of GBS was observed and the calculated relative risk was 6.2. Later studies have found that influenza vaccines contained structures that can induce anti-GM1 (ganglioside) antibodies after inoculation into mice. More recent information has suggested that the occurrence of GBS after currently used influenza and other vaccines is rare. GBS involves genetic and environmental factors, may be triggered by infections or vaccinations, and predisposition can be predicted by analyzing some of these factors.
机译:格林-巴利综合征(GBS)是一种罕见的自身免疫性疾病,在全球范围内,其发病率估计为0.6-4 / 100,000人/年。 GBS通常在患者出现呼吸道或胃肠道微生物感染症状后数天或数周发生。这种疾病在长达3到4周的几小时或几天内是亚急性的。空肠弯曲菌感染是所有格林-巴利综合征病例的三分之一。从GBS患者中分离出的空肠弯曲杆菌菌株具有脂环寡糖(LOS),具有类似GM1的结构。在人GBS的动物模型中证实了LOS和周围神经之间的分子模拟是GBS的原因。继1976年在美国实施“猪流感”病毒疫苗计划后,观察到GBS发生率增加,计算出的相对风险为6.2。后来的研究发现,流感疫苗所含的结构在接种到小鼠后可以诱导抗GM1(神经节苷脂)抗体。最近的信息表明,在目前使用的流感和其他疫苗之后,发生GBS的情况很少。 GBS涉及遗传和环境因素,可能由感染或疫苗接种触发,并且可以通过分析其中的一些因素来预测易感性。

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