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静脉注射用多价B族链球菌免疫球蛋白:概述

Polyvalent group B streptococcal immune globulin for intravenous administration: overview.

作者信息

Fischer G W, Hemming V G, Gloser H P, Bachmayer H, von Pilar C E, Wilson S R, Baron P A

机构信息

Department of Pediatrics, Uniformed Services University of the Health Sciences, Bethesda, Maryland 20814-4799.

出版信息

Rev Infect Dis. 1990 May-Jun;12 Suppl 4:S483-9; discussion S489-91. doi: 10.1093/clinids/12.supplement_4.s483.

Abstract

Immunoglobulin therapy is becoming an important modality for the prevention and treatment of bacterial and viral infection. Standard intravenous immunoglobulin (IVIG) is made from large pools of plasma obtained from normal blood donors. However, lot-to-lot variation in titers of antibody to specific microbial pathogens may diminish therapeutic efficacy. Since group B Streptococcus (GBS) is an important neonatal pathogen, a preparation with high titers of activity against GBS was prepared and studied. Plasma was obtained from volunteers immunized with a polyvalent GBS vaccine and was processed by the Swiss Red Cross for intravenous infusion. This high-titered GBS intravenous immunoglobulin (GBS-IVIG) was shown to be superior both in vitro and in vivo to standard IVIG. GBS-IVIG provided protection when therapy was delayed for up to 24 hours after infection. Standard IVIG did not protect animals against all GBS strains. However, GBS-IVIG enhanced survival from infection with all strains tested, even when the challenge dose of GBS was increased by 2 log units. Specific hyperimmune globulins to pathogens such as Haemophilus influenzae and Streptococcus pneumoniae have also been studied. Immunization of adult volunteers as a means of obtaining hyperimmune globulin appears to be an effective method of producing high-titered pathogen-specific preparations of IVIG.

摘要

免疫球蛋白疗法正成为预防和治疗细菌及病毒感染的一种重要方式。标准静脉注射免疫球蛋白(IVIG)由从正常献血者获取的大量血浆制成。然而,针对特定微生物病原体的抗体效价在批次间可能存在差异,这可能会降低治疗效果。由于B族链球菌(GBS)是一种重要的新生儿病原体,因此制备并研究了一种针对GBS具有高活性效价的制剂。血浆取自接种了多价GBS疫苗的志愿者,并由瑞士红十字会处理用于静脉输注。这种高滴度GBS静脉注射免疫球蛋白(GBS-IVIG)在体外和体内均显示出优于标准IVIG。当感染后治疗延迟长达24小时时,GBS-IVIG仍能提供保护。标准IVIG不能保护动物抵抗所有GBS菌株。然而,GBS-IVIG能提高所有测试菌株感染后的存活率,即使GBS的攻击剂量增加2个对数单位。针对诸如流感嗜血杆菌和肺炎链球菌等病原体的特异性高免疫球蛋白也已得到研究。将成年志愿者免疫作为获取高免疫球蛋白的一种手段,似乎是生产高滴度病原体特异性IVIG制剂的有效方法。

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