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不同IgG亚类抗体针对流感嗜血杆菌b型荚膜多糖的功能活性。

Functional activity of different IgG subclass antibodies against type b capsular polysaccharide of Haemophilus influenzae.

作者信息

Weinberg G A, Granoff D M, Nahm M H, Shackelford P G

出版信息

J Immunol. 1986 Jun 1;136(11):4232-6.

PMID:3486228
Abstract

The biologic activity of different human IgG subclass antibodies directed against the Haemophilus influenzae type b (Hib) capsular polysaccharide (PRP) was compared by using an in vitro complement-mediated bactericidal assay and an in vivo passive protection assay in infant rats. An IgG pool was made by Sephacryl S-300 chromatography of sera from adults immunized with PRP vaccine. An IgG2 subclass fraction was prepared by column immunoabsorption of the IgG pool with anti-IgG1 monoclonal antibody. An IgG1 subclass fraction was eluted from the affinity matrix. IgG1, IgG2, IgG3, and IgG4 concentrations in the fractions were measured by solid-phase competitive radioimmunoassays, and anti-PRP antibody was measured by a modified Farr assay. Each fraction was greater than 90% pure IgG2 or IgG1, respectively. There were no significant differences in the minimal anti-PRP antibody concentrations required to kill 50% of Hib cells in vitro (IgG, 0.22; IgG1, 0.21; and IgG2, 0.42 microgram/ml). Similarly, equivalent amounts of anti-PRP antibody of the IgG1 or IgG2 fractions protected against bacteremia (IgG1, 0.12; IgG2, 0.24 microgram per rat). IgG absorbed to remove anti-PRP antibody was neither bactericidal nor protective. Thus IgG1 and IgG2 anti-PRP antibody have equivalent functional activities against Hib as determined by these biologic assays.

摘要

通过体外补体介导的杀菌试验和幼鼠体内被动保护试验,比较了针对b型流感嗜血杆菌(Hib)荚膜多糖(PRP)的不同人IgG亚类抗体的生物学活性。用PRP疫苗免疫的成人血清经Sephacryl S - 300层析制备IgG池。用抗IgG1单克隆抗体通过柱免疫吸附法从IgG池中制备IgG2亚类组分。从亲和基质上洗脱得到IgG1亚类组分。用固相竞争性放射免疫分析法测定各组分中IgG1、IgG2、IgG3和IgG4的浓度,用改良的Farr分析法测定抗PRP抗体。各组分分别大于90%纯的IgG2或IgG1。体外杀死50% Hib细胞所需的最低抗PRP抗体浓度无显著差异(IgG为0.22;IgG1为0.21;IgG2为0.42微克/毫升)。同样,等量的IgG1或IgG2组分的抗PRP抗体可预防菌血症(IgG1为0.12;IgG2为0.24微克/只大鼠)。吸附去除抗PRP抗体的IgG既无杀菌作用也无保护作用。因此,通过这些生物学试验确定,IgG1和IgG2抗PRP抗体对Hib具有同等的功能活性。

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