Using Dried Blood Spots for a Sero-Surveillance Study of Maternally Derived Antibody against Group B Streptococcus
Using Dried Blood Spots for a Sero-Surveillance Study of Maternally Derived Antibody against Group B Streptococcus
Vaccination during pregnancy could protect women and their infants from invasive Group B Streptococcus (GBS) disease. To understand if neonatal dried blood spots (DBS) can be used to determine the amount of maternally derived antibody that protects infants against invasive GBS disease, a retrospective case-control study was conducted in England between 1 April 2014 and 30 April 2015. The DBS of cases with invasive GBS disease (n = 61) were matched with healthy controls (n = 125). The haematocrit, DBS storage temperature, freeze-thaw cycle, and paired serum/DBS studies were set up to optimise the antibody assessment. The samples were analysed using a multiplex immunoassay, and the results were assessed using parametric and nonparametric tests. Antibody concentrations were stable at haematocrits of up to 50% but declined at 75%. DBS storage at room temperature was stable for three months compared with storage from collection at -20 °C and rapidly degraded thereafter. Total IgG levels measured in DBS and paired serum showed a good correlation (r2 = 0.99). However, due to suboptimal storage conditions, no difference was found in the GBS IgG levels between DBS samples from cases and controls. We have demonstrated a proof of concept that assays utilising DBS for assessing GBS serotype-specific antibodies in infants is viable. This method could be used to facilitate future large sero-correlate studies, but DBS samples must be stored at -20 °C for long term preservation of antibody.
Auma, Erick
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Hall, Tom
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Chopra, Simran
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Bilton, Sam
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Ramkhelawon, Laxmee
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Amini, Fahimah
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Calvert, Anna
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Amirthalingam, Gayatri
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Jones, Christine E
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Andrews, Nick
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Heath, Paul T
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Le Doare, Kirsty
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4 February 2023
Auma, Erick
9698b65b-95cb-42af-8bf0-5c6849cda74f
Hall, Tom
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Chopra, Simran
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Bilton, Sam
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Ramkhelawon, Laxmee
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Amini, Fahimah
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Calvert, Anna
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Amirthalingam, Gayatri
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Jones, Christine E
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Andrews, Nick
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Heath, Paul T
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Le Doare, Kirsty
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Auma, Erick, Hall, Tom, Chopra, Simran, Bilton, Sam, Ramkhelawon, Laxmee, Amini, Fahimah, Calvert, Anna, Amirthalingam, Gayatri, Jones, Christine E, Andrews, Nick, Heath, Paul T and Le Doare, Kirsty
(2023)
Using Dried Blood Spots for a Sero-Surveillance Study of Maternally Derived Antibody against Group B Streptococcus.
Vaccines, 11 (2), [357].
(doi:10.3390/vaccines11020357).
Abstract
Vaccination during pregnancy could protect women and their infants from invasive Group B Streptococcus (GBS) disease. To understand if neonatal dried blood spots (DBS) can be used to determine the amount of maternally derived antibody that protects infants against invasive GBS disease, a retrospective case-control study was conducted in England between 1 April 2014 and 30 April 2015. The DBS of cases with invasive GBS disease (n = 61) were matched with healthy controls (n = 125). The haematocrit, DBS storage temperature, freeze-thaw cycle, and paired serum/DBS studies were set up to optimise the antibody assessment. The samples were analysed using a multiplex immunoassay, and the results were assessed using parametric and nonparametric tests. Antibody concentrations were stable at haematocrits of up to 50% but declined at 75%. DBS storage at room temperature was stable for three months compared with storage from collection at -20 °C and rapidly degraded thereafter. Total IgG levels measured in DBS and paired serum showed a good correlation (r2 = 0.99). However, due to suboptimal storage conditions, no difference was found in the GBS IgG levels between DBS samples from cases and controls. We have demonstrated a proof of concept that assays utilising DBS for assessing GBS serotype-specific antibodies in infants is viable. This method could be used to facilitate future large sero-correlate studies, but DBS samples must be stored at -20 °C for long term preservation of antibody.
Text
vaccines-11-00357
- Version of Record
More information
Accepted/In Press date: 27 January 2023
Published date: 4 February 2023
Additional Information:
Funding Information:
Collection of the DBS was funded by Pfizer Inc. USA. The funders had no input on the design or conduct of the study. The work was supported by the Medical Research Council (MR/SO165701/1).
Publisher Copyright:
© 2023 by the authors.
Identifiers
Local EPrints ID: 476154
URI: http://eprints.soton.ac.uk/id/eprint/476154
ISSN: 2076-393X
PURE UUID: 5c0b451b-90f0-42e9-a290-b868a0abe498
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Date deposited: 12 Apr 2023 16:56
Last modified: 17 Mar 2024 03:45
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Contributors
Author:
Erick Auma
Author:
Tom Hall
Author:
Simran Chopra
Author:
Sam Bilton
Author:
Laxmee Ramkhelawon
Author:
Fahimah Amini
Author:
Anna Calvert
Author:
Gayatri Amirthalingam
Author:
Nick Andrews
Author:
Paul T Heath
Author:
Kirsty Le Doare
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