Pneumococcal colonization impairs nasal and lung mucosal immune responses to Live Attenuated Influenza Vaccination in adults

Beatriz F. Carniel(Liverpool School of Tropical Medicine), Fernando Marcon(Liverpool School of Tropical Medicine), Jamie Rylance(Liverpool School of Tropical Medicine), Seher Zaidi(Liverpool School of Tropical Medicine), Jesús Reiné(Liverpool School of Tropical Medicine), Edessa Negera(Liverpool School of Tropical Medicine), Elissavet Nikolaou(Liverpool School of Tropical Medicine), Sherin Pojar(Liverpool School of Tropical Medicine), Carla Solórzano(Liverpool School of Tropical Medicine), Andrea M. Collins(Liverpool School of Tropical Medicine), Victoria Connor(Liverpool School of Tropical Medicine), Debby Bogaert(Nederlandse Vereniging voor Kindergeneeskunde), Stephen B. Gordon(University of Liverpool), Helder I. Nakaya(Universidade de São Paulo), Daniela M. Ferreira(Liverpool School of Tropical Medicine), Simon P. Jochems(Liverpool School of Tropical Medicine), Elena Mitsi(Liverpool School of Tropical Medicine)
medRxiv
February 25, 2020
Cited by 5Open Access
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Abstract

ABSTRACT Influenza virus infections affect millions of people annually. Current available vaccines provide varying rates of protection. There is a knowledge gap on how the nasal microbiota, particularly established pneumococcal colonization, shapes the response to influenza vaccination. In this study, we inoculated healthy adults with live S. pneumoniae and vaccinated them three days later with either TIV or LAIV. Vaccine-induced immune responses were assessed in nose, blood and lung. Nasal pneumococcal colonization had no impact upon TIV-induced antibody responses to influenza, which manifested in all compartments. However, pre-existing pneumococcal colonization dampened LAIV-mediated mucosal antibody responses, primarily IgA in the nose and IgG in the lung. Pulmonary influenza-specific cellular responses were more apparent in the LAIV group compared to either TIV or an unvaccinated group. These results indicate that TIV and LAIV elicit differential immunity to adults and that LAIV immunogenicity is diminished by the nasal presence of S. pneumoniae . This important confounder should be considered when assessing LAIV efficacy.


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