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Serum and mucosal antibody-mediated protection and identification of asymptomatic respiratory syncytial virus infection in community-dwelling older adults in Europe

Öner, D; Vernhes, C; Balla-Jhagjhoorsingh, S; Moureau, A; Crabbe, M; Salaun, B; Bastian, AR; Thys, K; De Smedt, J; Ooft, SN; et al. Öner, D; Vernhes, C; Balla-Jhagjhoorsingh, S; Moureau, A; Crabbe, M; Salaun, B; Bastian, AR; Thys, K; De Smedt, J; Ooft, SN; Korsten, K; Adriaenssens, N; Coenen, S; Butler, CC; Verheij, TJM; Drysdale, SB; Wildenbeest, JG; Pollard, AJ; Openshaw, PJM; Bont, L; Aerssens, J (2024) Serum and mucosal antibody-mediated protection and identification of asymptomatic respiratory syncytial virus infection in community-dwelling older adults in Europe. Frontiers in Immunology, 15. p. 1448578. ISSN 1664-3224 https://doi.org/10.3389/fimmu.2024.1448578
SGUL Authors: Drysdale, Simon Bruce

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Abstract

Introduction Respiratory syncytial virus (RSV) causes acute respiratory tract infection (ARTI) and reinfects adults throughout life, posing a risk for hospitalization in older adults (>60 years) with frailty and comorbidities. Methods To investigate serum and mucosal antibodies for protection against RSV infections, baseline serum samples were compared for RSV-pre- and -post-fusion (F) binding, and RSV-A2 neutralizing IgG antibodies between symptomatic RSV-ARTI (N = 30), non-RSV (RSV negative) ARTI (N = 386), and no ARTI (N = 338). Mucosal RSV-pre-F IgA and IgG levels, as well as serum RSV-G IgG antibodies, were analyzed to determine their association with protection from symptomatic RSV-ARTI in a subset study. Results Using a receiver operating characteristic (ROC) analysis, we established thresholds of 1.4- to 1.6-fold change (FC) for RSV-pre-F and -post-F, and RSV-A2 neutralizing IgG antibodies, respectively, enabling the identification of asymptomatic RSV cases with high sensitivity and specificity (>80% and >90%, respectively). As a result, serum RSV-pre-F, RSV-G IgG, and mucosal pre-F binding IgA antibodies showed correlations with protection against symptomatic RSV infection. RSV-pre-F IgG antibodies were correlated with protection from RSV infections irrespective of the symptoms. Discussion This study provides insights into antibody-mediated protection for symptomatic RSV infection in a community-dwelling older-adult population and establishes a threshold to identify asymptomatic RSV infection using a data-driven approach.

Item Type: Article
Additional Information: Copyright © 2024 Öner, Vernhes, Balla-Jhagjhoorsingh, Moureau, Crabbe, Salaun, Bastian, Thys, De Smedt, Ooft, Korsten, Adriaenssens, Coenen, Butler, Verheij, Drysdale, Wildenbeest, Pollard, Openshaw, Bont and Aerssens. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
Keywords: RSV infections, humoral immunity, immune correlates, immune response, older adults, respiratory syncytial virus, symptomatic infections, Humans, Respiratory Syncytial Virus Infections, Aged, Antibodies, Viral, Male, Female, Respiratory Syncytial Virus, Human, Immunoglobulin G, Europe, Antibodies, Neutralizing, Aged, 80 and over, Independent Living, Immunoglobulin A, Middle Aged, Asymptomatic Infections, Immunity, Mucosal
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Frontiers in Immunology
ISSN: 1664-3224
Language: eng
Media of Output: Electronic-eCollection
Related URLs:
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
116019Innovative Medicines Initiativehttps://doi.org/10.13039/501100010767
Dates:
Date Event
2024-10-18 Published
2024-09-17 Accepted
URI: https://openaccess.sgul.ac.uk/id/eprint/118333
Publisher's version: https://doi.org/10.3389/fimmu.2024.1448578

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