Development of a smartphone-based quantum dot lateral flow immunoassay strip for ultrasensitive detection of anti-SARS-CoV-2 IgG and neutralizing antibodies

•Quantum dot lateral flow immunoassay QD-LFIA was established for the detection of specific IgG and NAb to SARS-CoV-2.•The QD-LFIA was based on smartphones.•The QD-LFIA is ultrasensitive, cost-effective, rapid, and simple.•The QD-LFIA can be used for on-site detection in clinical practice. As severa...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of infectious diseases 2022-08, Vol.121, p.58-65
Hauptverfasser: Li, Jinfeng, Liu, Bochao, Tang, Xi, Wu, Ze, Lu, Jinhui, Liang, Chaolan, Hou, Shuiping, Zhang, Ling, Li, Tingting, Zhao, Wei, Fu, Yongshui, Ke, Yuebin, Li, Chengyao
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:•Quantum dot lateral flow immunoassay QD-LFIA was established for the detection of specific IgG and NAb to SARS-CoV-2.•The QD-LFIA was based on smartphones.•The QD-LFIA is ultrasensitive, cost-effective, rapid, and simple.•The QD-LFIA can be used for on-site detection in clinical practice. As several vaccines for SARS-CoV-2 have been developed, a large proportion of individuals have been vaccinated worldwide so far. The rapid and accurate immunoassays are urgently needed for detecting the specific virus-neutralizing antibody (NAb), which reflect the protective effect of the vaccines among different populations. In this study, we designed a quantum dot lateral flow immunoassay strip (QD-LFIA) for smartphones for the detection of specific IgG or neutralizing antibodies in SARS-CoV-2 in human serum or whole blood samples. The recombinant receptor binding domain of the SARS-CoV-2 spike protein was used as the antigen to combine with NAb or angiotensin-converting enzyme 2. Among 81 patients who recovered from COVID-19 who were diagnosed using the nucleic acid test initially, 98.8% (80/81) were positive for IgG and 88.9% (72/81) were positive for NAb by QD-LFIA. Among 64 individuals inoculated with inactivated vaccines and six subunit vaccines, 90% (63/70) were positive for IgG and 82.9% (58/70) were positive for NAb by QD-LFIA, whereas no cross-reaction was found in 150 healthy blood donors, two patients with influenza B, and three patients with common cold. The established platform could achieve a rapid and accurate detection of NAb specific to SARS-CoV-2, which could be used for detecting the protective effect of the vaccines in areas of world that currently affected by the pandemic.
ISSN:1201-9712
1878-3511
DOI:10.1016/j.ijid.2022.04.042