Sandra Romero-Steiner, Patricia F Holder, Patricia Gomez de Leon, Willie Spear, Thomas W Hennessy, George M Carlone
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引用次数: 31
Abstract
Determination of antibody avidity measurements can be difficult in human serum depending on the population evaluated. We evaluated three approaches for the determination of antibody avidity for immunoglobulin G (IgG). These approaches were (i) elution of bound antibody with increasing concentrations of a chaotropic agent using a single serum dilution, (ii) binding interference of multiple serum dilutions by a single concentration of a chaotrope, and (iii) elution of multiple serum dilutions by a single concentration of a chaotrope. Parameters that affect the determination of avidity measurements and their limitations were evaluated with pre- and post-Haemophilus influenzae type b conjugate vaccination sera (n=89). We determined that elution of low-avidity antibodies present in multiple dilutions of the serum sample by a single concentration of a chaotrope (0.15 M sodium thiocyanate [NaSCN]) was optimal for the determination of avidity measurements throughout a wide range of IgG concentrations (0.94 to 304.6 microg/ml). The percent reduction in concentration as determined by the elution assay with 0.15 M NaSCN correlated highly (r=0.84) with weighted averages obtained by an elution assay with multiple solutions of NaSCN. The correlation (r=0.57) between elution and binding interference, when a single concentration of a chaotrope was used, was lower than the correlation between the two elution methods (r=0.84). We found that the serum dilution, the heterogeneity of the antibody population, and the concentration of the chaotrope were the primary variables affecting avidity determinations. In this study, we present multiple analysis methods depending on the methodology used. We also present the factors that affect the analysis of avidity determinations given the polyclonal nature of human sera. This experimental approach should benefit the evaluation of similar antibodies induced by other bacterial polysaccharide vaccines.
根据评估人群的不同,在人血清中测定抗体亲和度可能是困难的。我们评估了测定免疫球蛋白G (IgG)抗体亲和力的三种方法。这些方法是(i)用单一血清稀释剂增加混乱剂浓度来洗脱结合抗体,(ii)用单一浓度的混乱剂来结合干扰多种血清稀释剂,(iii)用单一浓度的混乱剂来洗脱多种血清稀释剂。用b型流感嗜血杆菌结合疫苗接种前和接种后血清评估影响贪婪度测定的参数及其局限性(n=89)。我们确定,通过单一浓度的混乱剂(0.15 M硫氰酸钠[NaSCN])洗脱存在于多次稀释的血清样品中的低亲和度抗体,对于在广泛的IgG浓度范围内(0.94至304.6微克/毫升)测定亲和度测量是最佳的。0.15 M NaSCN洗脱法测定的浓度降低百分比与多种NaSCN溶液洗脱法所得的加权平均值高度相关(r=0.84)。当使用单一浓度的混乱物时,洗脱与结合干扰之间的相关性(r=0.57)低于两种洗脱方法之间的相关性(r=0.84)。我们发现血清稀释度、抗体群体的异质性和混乱物的浓度是影响抗体测定的主要变量。在本研究中,我们根据所使用的方法提出了多种分析方法。我们还提出了考虑到人血清的多克隆性质,影响贪婪测定分析的因素。该实验方法可用于评价其他细菌多糖疫苗诱导的类似抗体。