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Self-reactive IgG4 antibodies are associated with blocking of pathology in human lymphatic filariasis

机译:自活性IgG4抗体与人类淋巴丝体病变的阻断有关

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Lymphatic filariasis, a chronic disfiguring disease exhibits complex pathology. Based on different clinical manifestations, infected individuals are categorized into asymptomatic-carriers and chronic-patients. The mechanism behind differential clinical outcomes remains unclear. Roles of filaria-specific B cell responses in filariasis have been documented, whereas the contribution of B1 cell response and poly-specific IgG and IgA in the context of clinical filariasis is not deciphered. In this study, we measured the poly-specific IgG and IgA levels in different clinical categories of filariasis. Asymptomatic-carriers exhibited increased IgG4 antibodies against both filarial-antigens as well as auto-antigens compared to other clinical categories, although IgG against these auto-antigens remained lower. IgA levels against both filarial and auto-antigens were decreased in asymptomatic-carriers. A positive correlation between anti-filarial IgG4 and IgG4 against auto-antigens were observed, suggesting the synergistic role of poly-specific natural IgG4 with anti-filarial IgG4 in blocking the pathogenesis in asymptomatic microfilarial cases.
机译:淋巴丝虫病,一种慢性毁容疾病表现出复杂的病理学。基于不同的临床表现,受感染的个体分为无症状载体和慢性患者。差异临床结果背后的机制仍然不清楚。已经记录了丝体病毒中特异性B细胞反应的作用,而B1细胞反应和聚特异性IgG和IgA在临床丝虫病的上下文中的贡献则不会破坏。在这项研究中,我们测量了不同临床类别的丝虫病类别的多特异性IgG和IgA水平。与其他临床类别相比,无症状载体表现出对丝抗原的IgG4抗体以及自身抗原,尽管对这些自动抗原的IgG保持较低。在无症状载体中降低了对丝叶和自抗原的IgA水平。观察到抗丝状IgG4和IgG4与自身抗原的阳性相关性,表明聚特异性天然IgG4与抗丝状IgG4阻断无症状微型病例中的发病机制的协同作用。

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