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三种 ELISA 方案检测 RTS,S/AS01 诱导的抗 CSP IgG 抗体的相关性。

Correlations between three ELISA protocols measurements of RTS,S/AS01-induced anti-CSP IgG antibodies.

机构信息

KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.

Department of Biological Sciences, Pwani University, Kilifi, Kenya.

出版信息

PLoS One. 2023 May 23;18(5):e0286117. doi: 10.1371/journal.pone.0286117. eCollection 2023.

Abstract

BACKGROUND

RTS,S/AS01 induced anti-circumsporozoite protein (CSP) IgG antibodies are associated with the vaccine efficacy. There is currently no international standardisation of the assays used in the measurement of anti-CSP IgG antibody concentrations for use in evaluations of the vaccine's immunogenicity and/or efficacy. Here, we compared the levels of RTS,S/AS01 induced anti-CSP IgG antibodies measured using three different enzyme-Linked ImmunoSorbent Assays (ELISA).

METHODS

196 plasma samples were randomly selected from the 447 samples collected during the RTS,S/AS01 phase IIb trial in 2007 from Kenyan children aged between 5-17 months. The vaccine-induced anti-CSP IgG antibodies were then measured using two independently developed ELISA protocols ('Kilifi-RTS,S' and 'Oxford-R21') and compared to the results from the reference 'Ghent-RTS,S' protocol for the same participants. For each pair of protocols, a deming regression model was fitted. Linear equations were then derived to aid in conversions into equivalent ELISA units. The agreement was assessed using Bland and Altman method.

FINDINGS

The anti-CSP IgG antibodies measured from the three ELISA protocols were in agreement, and were positively and linearly correlated; 'Oxford' and 'Kilifi' r = 0.93 (95% CI 0.91-0.95), 'Oxford' and 'Ghent' r = 0.94 (95% CI: 0.92-0.96), and 'Kilifi' and 'Ghent' r = 0.97 (95% CI: 0.96-0.98), p<0.0001 for all correlations.

CONCLUSIONS

With the linearity, agreement and correlations established between the assays, conversion equations can be applied to convert results into equivalent units, enabling comparisons of immunogenicities across different vaccines of the same CSP antigens. This study highlights the need for the international harmonisation of anti-CSP antibody measurements.

摘要

背景

RTS,S/AS01 诱导的抗环子孢子蛋白(CSP)IgG 抗体与疫苗效力相关。目前,用于评估疫苗免疫原性和/或效力的抗 CSP IgG 抗体浓度测量中使用的检测方法没有国际标准化。在这里,我们比较了使用三种不同酶联免疫吸附测定(ELISA)测量的 RTS,S/AS01 诱导的抗 CSP IgG 抗体水平。

方法

从 2007 年肯尼亚 5-17 个月龄儿童中随机选择了 196 份来自 RTS,S/AS01 二期临床试验的 447 份血浆样本。然后使用两种独立开发的 ELISA 方案(“Kilifi-RTS,S”和“Oxford-R21”)测量疫苗诱导的抗 CSP IgG 抗体,并与同一参与者的参考“Ghent-RTS,S”方案的结果进行比较。对于每对方案,拟合了一个 Deming 回归模型。然后推导出线性方程以帮助转换为等效 ELISA 单位。使用 Bland 和 Altman 方法评估一致性。

结果

三种 ELISA 方案测量的抗 CSP IgG 抗体一致,呈正相关且线性相关;“Oxford”和“Kilifi”r = 0.93(95%CI 0.91-0.95),“Oxford”和“Ghent”r = 0.94(95%CI:0.92-0.96),“Kilifi”和“Ghent”r = 0.97(95%CI:0.96-0.98),所有相关性均为 p<0.0001。

结论

鉴于检测之间的线性、一致性和相关性,转换方程可用于将结果转换为等效单位,从而能够比较具有相同 CSP 抗原的不同疫苗的免疫原性。本研究强调了需要对 CSP 抗体测量进行国际协调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/90eb/10204981/03a6f7bc213e/pone.0286117.g001.jpg

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