Pneumococcal colonization impairs mucosal immune responses to live attenuated influenza vaccine

Beatriz F. Carniel(Liverpool School of Tropical Medicine), Fernando Marcon(Liverpool School of Tropical Medicine), Jamie Rylance(Liverpool School of Tropical Medicine), Esther L. German(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(University Medical Center Utrecht), 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)
JCI Insight
January 26, 2021
Cited by 35Open Access
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Abstract

Influenza virus infections affect millions of people annually, and current available vaccines provide varying rates of protection. However, the way in which the nasal microbiota, particularly established pneumococcal colonization, shape the response to influenza vaccination is not yet fully understood. In this study, we inoculated healthy adults with live Streptococcus pneumoniae and vaccinated them 3 days later with either tetravalent-inactivated influenza vaccine (TIV) or live attenuated influenza vaccine (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, experimentally induced 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 with either the 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. Therefore, nasopharyngeal pneumococcal colonization may affect LAIV efficacy.


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