Abstract
The ongoing SARS-CoV-2 pandemic was initially managed by non-pharmaceutical interventions such as diagnostic testing, isolation of positive cases, physical distancing and lockdowns. The advent of vaccines has provided crucial protection against SARS-CoV-2. Neutralising antibody (nAb) responses are a key correlate of protection, and therefore measuring nAb responses is essential for monitoring vaccine efficacy. Fingerstick dried blood spots (DBS) are ideal for use in large-scale sero-surveillance because they are inexpensive, offer the option of self-collection and can be transported and stored at ambient temperatures. Such advantages also make DBS appealing to use in resource-limited settings and in potential future pandemics. In this study, nAb responses in sera, venous blood and fingerstick blood stored on filter paper were measured. Samples were collected from SARS-CoV-2 acutely infected individuals, SARS-CoV-2 convalescent individuals and SARS-CoV-2 vaccinated individuals. Good agreement was observed between the nAb responses measured in eluted DBS and paired sera. Stability of nAb responses was also observed in sera stored on filter paper at room temperature for 28 days. Overall, this study provides support for the use of filter paper as a viable sample collection method to study nAb responses.
Original language | English |
---|---|
Article number | 15014 |
Number of pages | 12 |
Journal | Scientific Reports |
Volume | 13 |
Issue number | 1 |
Early online date | 11 Sept 2023 |
DOIs | |
Publication status | Published - Dec 2023 |
Bibliographical note
Funding Information:This work was supported by the University of Liverpool. This research was funded in part by the National Institute for Health and Care Research (CO-CIN-01) and jointly by NIHR and UK Research and Innovation (CV220-169, MC_PC_19059).
We thank the study participants and their families for their contributions. We thank all ISARIC4C Consortium Investigators. We also thank all the frontline NHS clinical and research staff as well as volunteer medical students, who collected the clinical data in challenging circumstances and aided in the collection of the study specimens. This work uses data provided by patients and collected by the NHS as part of their care and support #DataSavesLives. We would also like to thank Dr Andrew Owens for providing the HEK293T/ACE-2 cells. W.A. was funded under a Saudi Arabia grant (1074237684) in association with the Department Clinical Laboratory Sciences, College of Applied Medical Sciences, Sakakah 72388, the University of Aljouf, Saudi Arabia. A.A. was funded under a Saudi Arabia grant (NJU246) in association with the Department of Medical Microbiology, College of Applied Medical Sciences, Najran University, Najran, Saudi Arabia. F.B. was funded by a Wellcome Trust PhD studentship (102172/B/13/Z). L.T. was supported by a Wellcome Trust fellowship (205228/Z/16/Z). L.T. is also supported by the U.S. Food and Drug Administration Medical Countermeasures Initiative contract (75F40120C00085). L.T. and M.S. are supported by the National Institute for Health Research Health Protection Research Unit (HPRU) in Emerging and Zoonotic Infections (NIHR200907) at University of Liverpool in partnership with Public Health England (PHE), in collaboration with Liverpool School of Tropical Medicine and the University of Oxford. L.T. and M.S. are based at University of Liverpool. The views expressed in this article are those of the author(s) and not necessarily those of the NHS, UK Health Security Agency, UKRI, NIHR, or the Department of Health and Social Care. For the purpose of Open Access, the author has applied a CC BY public copyright licence to any Author Accepted Manuscript version arising from this submission. F.B. was funded by a Wellcome Trust PhD studentship (102172/B/13/Z).
Publisher Copyright:
© 2023, Springer Nature Limited.
ASJC Scopus subject areas
- General