用数学分析方法评价人免疫球蛋白制剂中乙型肝炎病毒表面抗原抗体效价的可能性

E. L. Postnova, A. A. Movsesyants
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引用次数: 0

摘要

科学的相关性。抗乙型肝炎病毒表面抗原(HBsAg)免疫球蛋白用于成人和儿童接触后预防乙型肝炎和治疗轻中度急性病毒性乙型肝炎。人免疫球蛋白制剂的临床有效性取决于其效力,而效力是通过对乙型肝炎病毒表面抗原(抗hbs抗体)的抗体含量来评估的。目前,这种评估涉及使用免疫测定技术,如酶联免疫吸附测定(ELISA)。的目标。本研究探讨了几种数学方法,用于分析基于elisa的人免疫球蛋白制剂的抗hbs抗体效价测定中获得的实验数据。材料和方法。本研究采用人抗hbs免疫球蛋白国际标准,两种免疫球蛋白制剂,ELISA检测试剂盒对血清或血浆样品中抗hbs抗体进行检测和定量。结果。采用夹心ELISA法,确定了测定的抗- hbs抗体浓度取决于校准曲线计算方法的选择(即手工分析、使用paralline软件的平行线分析、线性回归和4参数logistic回归)。测定的抗hbs抗体浓度变化±19 IU/mL。根据研究结果,错误选择数据分析方法可能导致测试样品中分析物效价(浓度)的错误计算。结论。该研究表明,需要改进数学方法来评估用于测定人免疫球蛋白制剂中抗hbs抗体浓度的实验数据。考虑到生物分析方法的要求和可用设备的能力,必须从手动计算切换到自动计算(例如,使用4参数逻辑模型)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Possibility of using mathematical analysis methods to evaluate the potency of antibodies to hepatitis B virus surface antigen in human immunoglobulin preparations
Scientific relevance. Anti-hepatitis B virus surface-antigen (HBsAg) immunoglobulins are used to prevent hepatitis B in adults and children after exposure and to treat mild to moderate acute viral hepatitis B. The clinical effectiveness of human immunoglobulin preparations is determined by their potency, which is assessed by the content of antibodies to hepatitis B virus surface antigen (anti-HBs antibodies). Currently, this assessment involves using immunoassay techniques, such as enzyme-linked immunosorbent assay (ELISA). Aim. This study examined several mathematical methods for analysing the experimental data obtained in ELISA-based anti-HBs antibody potency assays of human immunoglobulin preparations. Materials and methods. This study used the international standard for human anti-HBs immunoglobulin, two immunoglobulin preparations, and an ELISA test kit for the detection and quantification of anti-HBs antibodies in serum or plasma samples. Results. Using sandwich ELISA, the authors ascertained that the measured anti-HBs antibody concentration depended on the choice of calibration curve calculation method (i.e. manual analysis, parallel-line analysis using PARALINE software, linear regression, and 4-parameter logistic regression). The measured anti-HBs antibody concentrations varied by ± 19 IU/mL. According to the study results, an incorrectly selected method of data analysis can lead to an erroneous calculation of the analyte potency (concentration) in the test sample. Conclusions. The study demonstrated the need for improved mathematical methods for the evaluation of experimental data used to determine the anti-HBs antibody concentration in human immunoglobulin preparations. It is essential to switch from manual to automated calculation (for example, using a 4-parameter logistic model), taking into account the requirements for bioanalytical methods and the capabilities of the available equipment.
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