Child Salivary SIgA and Its Relationship to Enteric Infections and EED Biomarkers in Maputo, Mozambique

Frederick G. B. Goddard, Jacqueline Knee, Trent Sumner, Rassul Nalá, Thomas Clasen and Joe Brown
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Frederick G. B. Goddard: Gangarosa Department of Environmental Health, Rollins School of Public Health, Emory University, Atlanta, GA 30322, USA
Jacqueline Knee: School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA
Trent Sumner: School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA
Rassul Nalá: Instituto Nacional de Saúde-Ministério da Saúde Maputo-Mozambique, C.P. 264, Mozambique
Thomas Clasen: Gangarosa Department of Environmental Health, Rollins School of Public Health, Emory University, Atlanta, GA 30322, USA
Joe Brown: School of Civil and Environmental Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA

IJERPH, 2020, vol. 17, issue 9, 1-10

Abstract: Characterizing child immunological responses to enteric infections with antibody detection in serum can be challenging in resource-constrained field settings, because sample collection requires trained individuals and its invasive procedure may lead to low response rates, especially among children. Saliva may present a promising non-invasive alternative. The objectives of this research were to compare salivary antibody levels in children to enteric infections and biomarkers of environmental enteric dysfunction (EED). We collected saliva samples from children aged one to six years enrolled in a sanitation trial in Maputo, Mozambique, and characterized salivary secretory immunoglobulin A (SIgA) concentrations with enzyme-linked immunosorbent assays. We used multilevel linear models to analyze cross-sectional associations between salivary SIgA and the number of concurrent enteric pathogen infections, as well as EED biomarkers in matched stool samples. Median salivary SIgA concentrations in this study population were 54 μg/mL (inter-quartile range (IQR): 34, 85 μg/mL), and SIgA levels were similar between children of different ages. SIgA was lower in children experiencing a higher number of concurrent infections −0.04 log μg/mL (95% confidence interval (CI): −0.08 to −0.005 log μg/mL), but was not associated with any of the included EED biomarkers. Contrary to evidence from high-income countries that suggests salivary SIgA increases rapidly with age in young children, the high prevalence of enteric infections may have led to a suppression of immunological development in this study sample and could in part explain the similar SIgA levels between children of different ages.

Keywords: salivary antibodies; immunology; infectious diseases; enteric pathogens; global health (search for similar items in EconPapers)
JEL-codes: I I1 I3 Q Q5 (search for similar items in EconPapers)
Date: 2020
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