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定量抗 PA IgG ELISA;山羊中与炭疽毒素中和测定法的评估和可比性。

Quantitative anti-PA IgG ELISA; assessment and comparability with the anthrax toxin neutralization assay in goats.

机构信息

Department of Veterinary Tropical Diseases, University of Pretoria, Onderstepoort 0110, South Africa.

出版信息

BMC Vet Res. 2013 Dec 27;9:265. doi: 10.1186/1746-6148-9-265.

Abstract

BACKGROUND

Presently, few data exist on the level and duration of anti-protective antigen (PA) IgG in vaccinated livestock. Various adaptation of enzyme-linked immunosorbent assays (ELISAs) have been developed in studies to assess immune response following vaccination, albeit mostly in laboratory rodent models. The quantitative anti-anthrax IgG ELISA in this study describes a method of enumerating the concentration of anti-PA specific IgG present in sera of immunized goats, with the aid of an affinity-purified caprine polyclonal anti-anthrax PA-83 IgG standard. This was compared with the anthrax toxin neutralization assay (TNA) which measures a functional subset of toxin neutralizing anti-PA IgG.

RESULTS

The measured concentrations obtained in the standard curve correlated with the known concentration at each dilution. Percentage recovery of the standard concentrations ranged from 89 to 98% (lower and upper asymptote respectively). Mean correlation coefficient (r2) of the standard curve was 0.998. Evaluation of the intra-assay coefficient of variation showed ranges of 0.23-16.90% and 0.40-12.46% for days 28 and 140 sera samples respectively, following vaccination. The mean inter-assay coefficient of variation for triplicate samples repeated on 5 different days was 18.53 and 12.17% for days 28 and 140 sera samples respectively. Spearman's rank correlation of log-transformed IgG concentrations and TNA titres showed strong positive correlation (rs = 0.942; p = 0.01).

CONCLUSION

This study provides evidence that an indirect ELISA can be used for the quantification of anti-anthrax PA IgG in goats with the added advantage of using single dilutions to save time and resources. The use of such related immunoassays can serve as potential adjuncts to potency tests for Sterne and other vaccine types under development in ruminant species. This is the first report on the correlation of polyclonal anti-anthrax PA83 antibody with the TNA in goats.

摘要

背景

目前,关于接种疫苗的牲畜中抗保护性抗原 (PA) IgG 的水平和持续时间的数据很少。尽管大多数研究都是在实验室啮齿动物模型中进行的,但已经开发出各种酶联免疫吸附测定 (ELISA) 来评估疫苗接种后的免疫反应。本研究中的定量抗炭疽 IgG ELISA 描述了一种在免疫山羊血清中计数存在的抗-PA 特异性 IgG 浓度的方法,该方法借助亲和纯化的山羊多克隆抗炭疽 PA-83 IgG 标准品。这与炭疽毒素中和测定 (TNA) 进行了比较,该测定测量了毒素中和抗-PA IgG 的功能亚群。

结果

标准曲线中测量的浓度与每个稀释度的已知浓度相关。标准浓度的回收率范围为 89%至 98%(下限和上限渐近线分别)。标准曲线的平均相关系数 (r2) 为 0.998。评估日内变异系数显示,接种后第 28 天和第 140 天血清样本的范围分别为 0.23-16.90%和 0.40-12.46%。在 5 天的不同时间重复进行的三重复样本的平均日间变异系数分别为第 28 天和第 140 天血清样本的 18.53%和 12.17%。对 log 转换后的 IgG 浓度和 TNA 滴度进行 Spearman 秩相关分析显示,两者呈强正相关(rs=0.942;p=0.01)。

结论

本研究提供了证据表明,间接 ELISA 可用于定量山羊中的抗炭疽 PA IgG,并且使用单一稀释液可节省时间和资源,这是一个额外的优势。在绵羊和其他正在开发的反刍动物疫苗类型中,此类相关免疫测定可作为效力测试的潜在辅助手段。这是首次报道山羊中多克隆抗炭疽 PA83 抗体与 TNA 的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1a4/3892015/328a23653cf9/1746-6148-9-265-1.jpg

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