Using Dried Blood Spots for a Sero-Surveillance Study of Maternally Derived Antibody against Group B Streptococcus

Author:

Auma Erick12,Hall Tom2,Chopra Simran3,Bilton Sam4,Ramkhelawon Laxmee2,Amini Fahimah2,Calvert Anna2ORCID,Amirthalingam Gayatri5,Jones Christine E.267ORCID,Andrews Nick5,Heath Paul T.2ORCID,Le Doare Kirsty289

Affiliation:

1. Department of Biology, Université Claude Bernard Lyon, ENS de Lyon, CNRS, UMR, 69100 Villeurbanne, France

2. Centre for Neonatal and Paediatric Infection, Institute for Infection and Immunity, St George’s, University of London, London SW17 0RE, UK

3. Immunity and Infection, Faculty of Medicine, Imperial College London, London SW7 2BX, UK

4. Neonatal Unit, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford OX3 9DU, UK

5. Immunisation and Vaccine Preventable Diseases Division, UK Health Security Agency, London NW9 5EQ, UK

6. Faculty of Medicine and Institute for Life Sciences, University of Southampton, Southampton, SO16 6YD, UK

7. NIHR Southampton Clinical Research Facility and Biomedical Research Centre, University Hospital Southampton NHS Foundation Trust, Southampton SO16 6YD, UK

8. Makerere University—Johns Hopkins University Research Collaboration, Kampala P.O. Box 23491, Uganda

9. Pathogen Immunology Group, UK Health Security Agency, Porton Down, Salisbury SP4 0JG, UK

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.

Funder

Pfizer Inc. USA

Medical Research Council

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Drug Discovery,Pharmacology,Immunology

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