IgA对呼吸道病毒灭活的机制,包括上皮内中和

Mary B. Mazanec , Yung T. Huang , Sanjay W. Pimplikar , Michael E. Lamm
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引用次数: 12

摘要

IgA被认为在呼吸道和其他粘膜中提供三个级别的抗病毒保护。首先,IgA抗体可以与游离病毒粒子结合,阻止它们粘附上皮。其次,由于IgA通过聚合免疫球蛋白受体(pIgR)通过上皮细胞主动转运进入粘膜分泌物,IgA可能能够通过与新合成的病毒蛋白结合而中断感染上皮细胞内的病毒产生。最后,由于粘膜免疫球蛋白是由固有层的浆细胞产生的,IgA抗体可以通过pIgR将上皮细胞释放的病毒抗原运送回粘膜分泌物中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanisms of inactivation of respiratory viruses by IgA, including intraepithelial neutralization

IgA is thought to provide three levels of anti-viral protection in the respiratory and other mucous membranes. First, IgA antibodies can complex with free virions, preventing their adhesion to the epithelium. Second, since IgA is actively transported by the polymeric immunoglobulin receptor (pIgR) through epithelial cells into the mucosal secretions, IgA may be able to interrupt virus production within infected epithelial cells by binding to newly synthesized viral proteins. Finally, since mucosal immunoglobulins are produced by plasma cells in the lamina propria, IgA antibodies, via the pIgR, can potentially shuttle viral antigens released from epithelial cells back into the mucosal secretions.

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