Mao Naiying, Dong Mei, Zhu Zhen, Huang Qi, Yu Xiali, Xie Hui, Dong Jianping, Sun Jingyi, Huang Fang, Xu Wenbo
NHC Key Laboratory of Medical Virology and Viral Diseases, WHO WPRO Regional Reference Laboratory of Measles and Rubella, Measles Laboratory in National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
Institute for Immunization and Prevention, Beijing Center for Disease Control and Prevention, Beijing Academy for Preventive Medicine, Beijing Institute of Tuberculosis Control Research and Prevention, Beijing, China.
China CDC Wkly. 2022 Oct 7;4(40):890-894. doi: 10.46234/ccdcw2022.185.
Oral fluids (OFs) have been broadly used as non-invasive samples for evaluating protective IgG antibodies from natural infection or vaccination, especially in pediatric populations.
Paired OF and serum were collected from both individuals who received a booster dose of the inactive coronavirus disease 2019 (COVID-19) vaccine as well as those who did not have a history of COVID-19 vaccination and infection (as the control group). The total human IgG antibody (HIgG) content was evaluated as a marker of OF sampling quality. An in-house adapted magnetic particle-based chemiluminescence immunoassay was used for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) IgG antibody detection in the OF. The SARS-CoV-2 IgG antibody in the serum samples was detected using a commercial immunoassay.
In total, 579 paired OF and serum samples were collected. An additional 172 OF samples were collected from preschool children. The results indicated that the HIgG concentration in qualified OF samples should be higher than 0.3 µg/mL. Compared to the serum assay, the in-house OF immunoassay for detecting IgG antibodies against SARS-CoV-2 had 95.06% accuracy, 95.03% sensitivity, and 100% specificity.
Overall, the in-house immunoassay for detecting SARS-CoV-2 IgG antibodies in OF showed high potential for application towards serological surveillance and immunization effect assessment after large-scale, inactive COVID-19 vaccination in China.
口腔液(OFs)已被广泛用作非侵入性样本,用于评估自然感染或疫苗接种产生的保护性IgG抗体,尤其是在儿科人群中。
收集了接受2019年冠状病毒病(COVID-19)灭活疫苗加强剂量的个体以及无COVID-19疫苗接种和感染史的个体(作为对照组)的配对口腔液和血清。评估总人IgG抗体(HIgG)含量作为口腔液采样质量的标志物。采用内部改良的基于磁颗粒的化学发光免疫分析法检测口腔液中的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)IgG抗体。血清样本中的SARS-CoV-2 IgG抗体采用商业免疫分析法检测。
总共收集了579对口腔液和血清样本。另外从学龄前儿童中收集了172份口腔液样本。结果表明,合格口腔液样本中的HIgG浓度应高于0.3μg/mL。与血清检测相比,用于检测抗SARS-CoV-2 IgG抗体的内部口腔液免疫分析法的准确率为95.06%,灵敏度为95.03%,特异性为100%。
总体而言,用于检测口腔液中SARS-CoV-2 IgG抗体的内部免疫分析法在中国大规模接种COVID-19灭活疫苗后的血清学监测和免疫效果评估方面显示出很高的应用潜力。