Quantity and Quality of Naturally Acquired Antibody Immunity to the Pneumococcal Proteome Throughout Life

Author:

Vissers Marloes1,van de Garde Martijn D B1ORCID,He Samantha W J1,Brandsen Milou1,Hendriksen Rosanne1,Nicolaie Mioara Alina2,van der Maas Larissa3,Meiring Hugo D3,van Els Cecile A C M14,van Beek Josine1,Rots Nynke Y1ORCID

Affiliation:

1. Centre for Infectious Disease Control, National Institute for Public Health and the Environment , Bilthoven , The Netherlands

2. Expertise Centre for Methodology and Information Services, National Institute for Public Health and the Environment , Bilthoven , The Netherlands

3. Product Characterization and Formulation, Institute for Translational Vaccinology , Bilthoven , The Netherlands

4. Infectious Diseases and Immunology, Department of Biomolecular Health Sciences, Faculty of Veterinary Medicine, Utrecht University , Utrecht , The Netherlands

Abstract

Abstract Background Young children and older adults are susceptible for invasive pneumococcal disease (IPD) caused by Streptococcus pneumoniae. Pneumococcal protein-specific antibodies play a protective role against IPD; however, not much is known about the pace of acquisition, maturation, and maintenance of these antibodies throughout life. Methods Immunoglobulin G (IgG) and IgA levels, avidity, and/or specificity to the pneumococcal proteome in serum and saliva from healthy young children, adults, and older adults, with known carriage status, were measured by enzyme-linked immunosorbent assay (ELISA) and 2-dimensional western blotting against ΔcpsTIGR4. Results Eleven-month-old children, the youngest age group tested, had the lowest pneumococcal proteome-specific IgG and IgA levels and avidity in serum and saliva, followed by 24-month-old children and were further elevated in adult groups. Among adult groups, the parents had the highest serum and saliva IgG and IgA antibody levels. In children, antibody levels and avidity correlated with daycare attendance and presence of siblings, posing as proxy for exposure and immunization. Immunodominance patterns slightly varied throughout life. Conclusions Humoral immunity against the pneumococcal proteome is acquired through multiple episodes of pneumococcal exposure. Low-level and low-avidity antiproteome antibody profiles in young children may contribute to their IPD susceptibility, while in overall antiproteome antibody-proficient older adults other factors likely play a role.

Funder

Ministry of Health, Welfare and Sport

Publisher

Oxford University Press (OUP)

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