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Determination of echinococcosis IgG antibodies using magnetic bead-based chemiluminescence immunoassay.
Chen, Cuicui; Liang, Huankun; Peng, Fenglan; Zhong, Shuhai; Lu, Yanhong; Guo, Guiling; Li, Laiqing.
Afiliação
  • Chen C; Guangzhou Youdi Bio-Technology Co., Ltd., Guangzhou 510663, China; Jinan Laide Biotechnology Co., Ltd., Jinan 271100, China.
  • Liang H; Guangzhou Youdi Bio-Technology Co., Ltd., Guangzhou 510663, China.
  • Peng F; Taian Disabled Soldiers' Hospital of Shandong Province, Taian 271099, China.
  • Zhong S; Guangzhou Youdi Bio-Technology Co., Ltd., Guangzhou 510663, China.
  • Lu Y; Guangzhou Youdi Bio-Technology Co., Ltd., Guangzhou 510663, China.
  • Guo G; Guangzhou Youdi Bio-Technology Co., Ltd., Guangzhou 510663, China.
  • Li L; Guangzhou Youdi Bio-Technology Co., Ltd., Guangzhou 510663, China; Jinan Laide Biotechnology Co., Ltd., Jinan 271100, China. Electronic address: lilaiqing191@163.com.
J Immunol Methods ; 520: 113513, 2023 09.
Article em En | MEDLINE | ID: mdl-37307908
ABSTRACT
Echinococcosis is a kind of parasitic disease shared by humans and animals. The aim of this study was to establish a new detection method for echinococcosis screening using magnetic bead-based chemiluminescence immunoassay (CLIA). A magnetic bead-based CLIA to determine anti-echinococcosis IgG antibodies was optimized and established. The sensitivity, accuracy, precision and recovery rate were evaluated using the national reference serum, and the reference interval, specificity and comparison assays were performed using the clinical negative/positive echinococcosis serum samples. This study established a new CLIA to determine anti-echinococcosis IgG antibodies. The sensitivity of this CLIA method was higher than that of the registered ELISA kit and the national standard, the conformance rate of the negative/positive references was 100% (8/8), the CVs of the sensitivity reference were all below 5%, and the CVs of the precision reference were 5.7%. There was no obvious cross-reactivity with the common parasitic disease-positive serum and serum interferents. Clinical sample testing found that the cutoff value of this CLIA was 5537.15 (RLU), and there was no significant difference between the CLIA method and the registered ELISA kit. This study established a fully automated CLIA method with high sensitivity, specificity, accuracy, precision, recovery rate, and satisfactory clinical testing performance, which may provide a new choice for echinococcosis screening.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunoglobulina G / Luminescência Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Imunoglobulina G / Luminescência Idioma: En Ano de publicação: 2023 Tipo de documento: Article