医学
慢性炎症性脱髓鞘性多发性神经病
免疫学
重症肌无力
皮肌炎
静脉注射免疫球蛋白
格林-巴利综合征
抗体
血小板减少性紫癜
血液学
川崎病
免疫系统
自身免疫性疾病
自身免疫
内科学
动脉
作者
Amal Ephrem,Namita Misra,Ghada S. Hassan,Suryasarathi Dasgupta,Sandrine Delignat,J.P. Duong Van Huyen,Soulaïma Chamat,Fabienne Prost,Sébastien Lacroix‐Desmazes,S. V. Kavery,M Kazatchkine
标识
DOI:10.1007/s10238-005-0079-y
摘要
Intravenous immunoglobulin (IVIg) has been used in the treatment of primary and secondary antibody deficiencies for over two decades. Since the early 1980s, the therapeutic efficacy of IVIg has been established in idiopathic thrombocytopenic purpura, Guillain-Barré syndrome, chronic inflammatory demyelinating polyneuropathy, myasthenia gravis, dermatomyositis and Kawasaki syndrome, and the prevention of graft versus host disease in recipients of allogeneic bone marrow transplants. Its use has also been reported in a large number of other autoimmune and systemic inflammatory conditions. In this review, we discuss the mechanisms by which IVIg exerts immunomodulatory effects in immune pathologies.
科研通智能强力驱动
Strongly Powered by AbleSci AI