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Detection of SARS-CoV-2 antibodies in serum and dried blood spot samples of vaccinated individuals using a sensitive homogeneous proximity extension assay
Uppsala University, Science for Life Laboratory, SciLifeLab. Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Immunology, Genetics and Pathology, Molecular Tools and Functional Genomics. Unit Affin Prote Uppsala, Sci Life Lab, Stockholm, Sweden.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Immunology, Genetics and Pathology, Molecular Tools and Functional Genomics. Uppsala University, Science for Life Laboratory, SciLifeLab.
Uppsala University, Science for Life Laboratory, SciLifeLab. Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Immunology, Genetics and Pathology, Molecular Tools and Functional Genomics.
Uppsala University, Science for Life Laboratory, SciLifeLab. Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Immunology, Genetics and Pathology, Molecular Tools and Functional Genomics. Unit Affin Prote Uppsala, Sci Life Lab, Stockholm, Sweden.
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2022 (English)In: New Biotechnology, ISSN 1871-6784, E-ISSN 1876-4347, Vol. 72, p. 139-148Article in journal (Refereed) Published
Abstract [en]

A homogeneous PCR-based assay for sensitive and specific detection of antibodies in serum or dried blood spots (DBS) is presented and the method is used to monitor individuals infected with or vaccinated against SARS-CoV-2. Detection probes were prepared by conjugating the recombinant spike protein subunit 1 (S1), containing the receptor binding domain (RBD) of SARS-CoV-2, to each of a pair of specific oligonucleotides. The same was done for the nucleocapsid protein (NP). Upon incubation with serum or DBS samples, the bi- or multivalency of the antibodies (IgG, IgA or IgM) brings pairs of viral proteins with their conjugated oligonucleotides in proximity, allowing the antibodies to be detected by a modified proximity extension assay (PEA). Anti-S1 and anti-NP antibodies could be detected simultaneously from one incubation reaction. This Antibody PEA (AbPEA) test uses only 1 µl of neat or up to 100,000-fold diluted serum or one ø1.2 mm disc cut from a DBS. All 100 investigated sera and 21 DBS collected prior to the COVID-19 outbreak were negative, demonstrating a 100% specificity. The area under the curve, as evaluated by Receiver Operating Characteristic (ROC) analysis reached 0.998 (95%CI: 0.993–1) for samples taken from 11 days after symptoms onset. The kinetics of antibody responses were monitored after a first and second vaccination using serially collected DBS from 14 individuals. AbPEA offers highly specific and sensitive solution-phase antibody detection without requirement for secondary antibodies, no elution step when using DBS sample in a simple procedure that lends itself to multiplex survey of antibody responses.

Place, publisher, year, edition, pages
Elsevier, 2022. Vol. 72, p. 139-148
Keywords [en]
Homogenous serological assay, PCR-based antibody detection, SARS-CoV-2 antibody, Proximity extension assay, Finger -prick dried blood spot, Multiplex immunoassay
National Category
Biochemistry Molecular Biology Infectious Medicine Immunology in the medical area
Identifiers
URN: urn:nbn:se:uu:diva-492677DOI: 10.1016/j.nbt.2022.11.004ISI: 000896515300004PubMedID: 36423830OAI: oai:DiVA.org:uu-492677DiVA, id: diva2:1725316
Funder
Science for Life Laboratory, SciLifeLabKnut and Alice Wallenberg Foundation, 2020.0182Swedish Foundation for Strategic Research, SB16-0046Swedish Research Council, 2020-02258Available from: 2023-01-10 Created: 2023-01-10 Last updated: 2025-02-20Bibliographically approved
In thesis
1. Advanced molecular tools for diagnostic analyses of RNA and antibodies in situ and in solution
Open this publication in new window or tab >>Advanced molecular tools for diagnostic analyses of RNA and antibodies in situ and in solution
2024 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Advanced molecular diagnostics uses in vitro biological assays to detect nucleic acids or proteins even in low concentrations across samples, allowing for the identification of biomarkers, monitoring the course of the disease over time, and selection of appropriate therapy. In this thesis, I focus on development and early applications of several molecular tools of expected value in research, and eventually also clinically. 

In papers I and II, proximity extension assay (PEA) was for the first time modified to measure specific antibody responses, rather than protein levels as in the standard PEA. We call the method AbPEA and the technique was used to sensitively measure antibody responses to the spike protein or the nucleocapsid of SARS-CoV-2. We demonstrated that AbPEA has high specificity, sensitivity, and broad dynamic range, along with multiplexing potential, offering performance similar to that of other methods for antibody measurements. We demonstrated utilization of blood and saliva samples in paper I and paper II, respectively, which further establish that our approach has great potential for large-scale screening and biobanking. 

In paper III, we aimed to investigate how the protein composition of extracellular vesicles (EVs) differed among blood samples collected from healthy individual or ones with either mild or severe COVID-19. Proximity barcoding assay was applied to obtain a comprehensive overview of the protein composition of large numbers of individual EVs, demonstrating interesting differences. 

In paper IV, we enhanced padlock-RCA-based RNA genotyping in situ by using another newly developed technology for highly selective detection of DNA or RNA sequence variants, referred to as super RCA (sRCA). Our analysis showed that this approach can improve the selectivity for sequence variants during in situ detection of mutant or wild-type transcripts, and the signals representing superRCA reaction products are prominent and easily distinguished from any background.

Place, publisher, year, edition, pages
Uppsala: Acta Universitatis Upsaliensis, 2024. p. 56
Series
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine, ISSN 1651-6206 ; 2016
Keywords
Homogenous serological assay, PCR-based antibody detection, Proximity extension assay, SARS-CoV-2 antibody, Extracellular vesicles, Proximity barcoding assay, in situ superRCA, mutant transcript
National Category
Medical Biotechnology
Identifiers
urn:nbn:se:uu:diva-522118 (URN)978-91-513-2029-8 (ISBN)
Public defence
2024-03-22, room A1:107a, BMC, Husargatan 3, Uppsala, 13:00 (English)
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Supervisors
Available from: 2024-02-29 Created: 2024-02-01 Last updated: 2024-02-29

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Zhao, HongxingWang, MengqiMuthelo, PhathutshedzoLöf, LizaGallini, RadiosaNilsson, KennethÅberg, MikaelKamali-Moghaddam, MasoodLandegren, Ulf

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Zhao, HongxingWang, MengqiMuthelo, PhathutshedzoLöf, LizaGallini, RadiosaNilsson, KennethÅberg, MikaelKamali-Moghaddam, MasoodLandegren, Ulf
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