Looney R John, Huggins Jennifer
Department of Medicine, Allergy, Immunology, Rheumatology Unit, School of Medicine and Dentistry, University of Rochester, 595 Elmwood Ave, Room G-6454, Rochester, NY 14642, USA.
Best Pract Res Clin Haematol. 2006;19(1):3-25. doi: 10.1016/j.beha.2005.01.032.
Intravenous immunoglobulin G (IVIG) has become increasingly important both as replacement therapy in primary and acquired humoral immunodeficiency and as an immunomodulatory therapy in autoimmune disease and transplantation. Multiple potential mechanisms for the effects of IVIG have now been recognized but the contribution of each mechanism in different diseases is uncertain. IVIG is generally well tolerated but serious side effects can occur and need to be addressed. IVIG has Food and Drug Administration (FDA) approval for a half dozen indications but these account for only about half the use of IVIG. This chapter reviews the development of IVIG for primary immunodeficiency, the evidence for efficacy of IVIG in autoimmune and inflammatory conditions, the risks associated with administration of IVIG, and steps that can be taken to minimize adverse events.
静脉注射免疫球蛋白G(IVIG)在原发性和获得性体液免疫缺陷的替代治疗以及自身免疫性疾病和移植中的免疫调节治疗方面都变得越来越重要。目前已经认识到IVIG作用的多种潜在机制,但每种机制在不同疾病中的作用尚不确定。IVIG一般耐受性良好,但可能会出现严重副作用,需要加以处理。IVIG已获得美国食品药品监督管理局(FDA)对六种适应症的批准,但这些仅占IVIG使用量的一半左右。本章回顾了IVIG用于原发性免疫缺陷的发展历程、IVIG在自身免疫和炎症性疾病中的疗效证据、IVIG给药相关风险以及可采取的将不良事件降至最低的措施。