Immunologic Testing for SARS-CoV-2 Infection from the Antigen Perspective
- PMID: 33318065
- PMCID: PMC8091849
- DOI: 10.1128/JCM.02160-20
Immunologic Testing for SARS-CoV-2 Infection from the Antigen Perspective
Abstract
Coronavirus disease 2019 (COVID-19), caused by the novel coronavirus severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has spread globally as a severe pandemic. SARS-CoV-2 infection stimulates antigen-specific antibody responses. Multiple serologic tests have been developed for SARS-CoV-2. However, which antigens are most suitable for serological testing remains poorly understood. Specifically, which antigens have the highest sensitivity and specificity for serological testing and which have the least cross-reactivity with other coronaviruses are currently unknown. Previous studies have shown that the S1 domain of the spike (S) protein has very low cross-reactivity between epidemic coronaviruses and common human coronaviruses, whereas the S2 domain of the S protein and the nucleocapsid protein (N protein) show low-level cross-reactivity. Therefore, S1 is considered more specific than the native homotrimer of the S protein, and the receptor-binding domain as an antigen to test patient antibodies is more sensitive than the native N protein. In addition, an increasing number of studies have used multiantigen protein arrays to screen serum from convalescent patients with COVID-19. Antigen combinations demonstrated improved performance compared to each individual antigen. For rapid antigen detection, the sensitivity of the test is higher in the first week of onset of the disease with high viral loads. Highly sensitive and specific immunological diagnostic methods for antibodies or those that directly detect viral antigens in clinical samples would be beneficial for the rapid and accurate diagnosis of SARS-CoV-2 infection.
Keywords: COVID-19; SARS-CoV-2; antigen; cross-reaction; serology testing.
Copyright © 2021 American Society for Microbiology.
Figures
Similar articles
-
Comparison of 2 fully automated tests detecting antibodies against nucleocapsid N and spike S1/S2 proteins in COVID-19.Diagn Microbiol Infect Dis. 2021 Jan;99(1):115197. doi: 10.1016/j.diagmicrobio.2020.115197. Epub 2020 Aug 29. Diagn Microbiol Infect Dis. 2021. PMID: 32977117 Free PMC article.
-
Evaluation of a multiplexed coronavirus antigen array for detection of SARS-CoV-2 specific IgG in COVID-19 convalescent plasma.J Immunol Methods. 2021 Oct;497:113104. doi: 10.1016/j.jim.2021.113104. Epub 2021 Jul 22. J Immunol Methods. 2021. PMID: 34303688 Free PMC article.
-
A Serological Snapshot of COVID-19 Initial Stages in Israel by a 6-Plex Antigen Array.Microbiol Spectr. 2021 Oct 31;9(2):e0087021. doi: 10.1128/Spectrum.00870-21. Epub 2021 Oct 6. Microbiol Spectr. 2021. PMID: 34612689 Free PMC article.
-
Serological antibody testing in the COVID-19 pandemic: their molecular basis and applications.Biochem Soc Trans. 2020 Dec 18;48(6):2851-2863. doi: 10.1042/BST20200744. Biochem Soc Trans. 2020. PMID: 33170924 Review.
-
Protein-based lateral flow assays for COVID-19 detection.Protein Eng Des Sel. 2021 Feb 15;34:gzab010. doi: 10.1093/protein/gzab010. Protein Eng Des Sel. 2021. PMID: 33991088 Free PMC article. Review.
Cited by
-
Systematic Study of Various Functionalization Steps for Ultrasensitive Detection of SARS-CoV-2 with Direct Laser-Functionalized Au-LIG Electrochemical Sensors.ACS Appl Mater Interfaces. 2024 Sep 18;16(37):49041-49052. doi: 10.1021/acsami.4c09571. Epub 2024 Sep 4. ACS Appl Mater Interfaces. 2024. PMID: 39231012 Free PMC article.
-
Performance Analysis of Serodiagnostic Tests to Characterize the Incline and Decline of the Individual Humoral Immune Response in COVID-19 Patients: Impact on Diagnostic Management.Viruses. 2024 Jan 6;16(1):91. doi: 10.3390/v16010091. Viruses. 2024. PMID: 38257792 Free PMC article.
-
Development and Clinical Performance of InteliSwab® COVID-19 Rapid Test: Evaluation of Antigen Test for the Diagnosis of SARS-CoV-2 and Analytical Sensitivity to Detect Variants of Concern Including Omicron and Subvariants.Viruses. 2023 Dec 29;16(1):61. doi: 10.3390/v16010061. Viruses. 2023. PMID: 38257761 Free PMC article.
-
Sensitivities of a Rapid Test Versus an ELISA Kit for Detecting Anti-SARS-CoV-2 IgM/IgG in Sera from an Egyptian Cohort.Curr Microbiol. 2023 Nov 30;81(1):24. doi: 10.1007/s00284-023-03473-z. Curr Microbiol. 2023. PMID: 38032503
-
B-Cell Epitopes-Based Chimeric Protein from SARS-CoV-2 N and S Proteins Is Recognized by Specific Antibodies in Serum and Urine Samples from Patients.Viruses. 2023 Sep 5;15(9):1877. doi: 10.3390/v15091877. Viruses. 2023. PMID: 37766284 Free PMC article.
References
-
- Cao Y, Su B, Guo X, Sun W, Deng Y, Bao L, Zhu Q, Zhang X, Zheng Y, Geng C, Chai X, He R, Li X, Lv Q, Zhu H, Deng W, Xu Y, Wang Y, Qiao L, Tan Y, Song L, Wang G, Du X, Gao N, Liu J, Xiao J, Su XD, Du Z, Feng Y, Qin C, Qin C, Jin R, Xie XS. 2020. Potent neutralizing antibodies against SARS-CoV-2 identified by high-throughput single-cell sequencing of convalescent patients’ B cells. Cell 182:73–84.e16. 10.1016/j.cell.2020.05.025. - DOI - PMC - PubMed
-
- He Q, Manopo I, Lu L, Leung BP, Chng HH, Ling AE, Chee LL, Chan SW, Ooi EE, Sin YL, Ang B, Kwang J. 2005. Novel immunofluorescence assay using recombinant nucleocapsid-spike fusion protein as antigen to detect antibodies against severe acute respiratory syndrome coronavirus. Clin Diagn Lab Immunol 12:321–328. 10.1128/CDLI.12.2.321-328.2005. - DOI - PMC - PubMed
-
- Lou B, Li TD, Zheng SF, Su YY, Li ZY, Liu W, Yu F, Ge SX, Zou QD, Yuan Q, Lin S, Hong CM, Yao XY, Zhang XJ, Wu DH, Zhou GL, Hou WH, Li TT, Zhang YL, Zhang SY, Fan J, Zhang J, Xia NS, Chen Y. 2020. Serology characteristics of SARS-CoV-2 infection after exposure and post-symptom onset. Eur Respir J 56:2000763. 10.1183/13993003.00763-2020. - DOI - PMC - PubMed
-
- Liu W, Liu L, Kou G, Zheng Y, Ding Y, Ni W, Wang Q, Tan L, Wu W, Tang S, Xiong Z, Zheng S. 2020. Evaluation of nucleocapsid and spike protein-based enzyme-linked immunosorbent assays for detecting antibodies against SARS-CoV-2. J Clin Microbiol 58:e00461-20. 10.1128/JCM.00461-20. - DOI - PMC - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous