Steele R W, Burks A W, Williams L W
Department of Pediatrics, University of Arkansas for Medical Sciences.
Ann Allergy. 1988 Feb;60(2):89-94.
At the present time there are three commercially available intravenous immunoglobulin (IVIG) preparations. There is no distinct therapeutic advantage for any one product over any other. Intravenous immunoglobulin is currently approved for the treatment of antibody deficiency syndromes and for acute and chronic idiopathic thrombocytopenic purpura. In addition, controlled clinical trials have demonstrated efficacy for the treatment of Kawasaki disease and for the prevention of the following infections: sepsis in preterm neonates, sepsis in infants with AIDS, and cytomegalovirus infection in the immune-compromised host. Open (uncontrolled) studies have suggested benefit in the treatment of neonatal sepsis, chronic Epstein-Barr virus infection, and a number of autoimmune diseases. Additional carefully designed studies must be completed before IVIG therapy can be recommended for these latter categories. In published reports, dosage of IVIG and intervals between infusions have varied considerably. For all current indications, the physician must therefore individualize treatment and thoroughly review any recent literature that may clarify guidelines to IVIG therapy. Significant adverse reactions are rare but high cost remains the main obstacle to more routine implementation.
目前有三种市售的静脉注射免疫球蛋白(IVIG)制剂。任何一种产品相对于其他产品都没有明显的治疗优势。静脉注射免疫球蛋白目前被批准用于治疗抗体缺乏综合征以及急性和慢性特发性血小板减少性紫癜。此外,对照临床试验已证明其对治疗川崎病以及预防以下感染有效:早产儿败血症、艾滋病婴儿败血症以及免疫功能低下宿主的巨细胞病毒感染。开放性(非对照)研究表明其对治疗新生儿败血症、慢性EB病毒感染以及多种自身免疫性疾病有益。在能推荐将IVIG疗法用于后几类疾病之前,必须完成更多精心设计的研究。在已发表的报告中,IVIG的剂量和输注间隔差异很大。因此,对于所有当前适应证,医生必须个体化治疗,并彻底查阅近期可能阐明IVIG治疗指南的文献。严重不良反应很少见,但高成本仍然是更常规应用的主要障碍。