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Innate and adaptive nasal mucosal immune responses following experimental human pneumococcal colonization

Jochems, SP; de Ruiter, K; Solórzano, C; Voskamp, A; Mitsi, E; Nikolaou, E; Carniel, BF; ... Ferreira, DM; + view all (2019) Innate and adaptive nasal mucosal immune responses following experimental human pneumococcal colonization. Journal of Clinical Investigation , 129 (10) pp. 4523-4538. 10.1172/JCI128865. Green open access

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Abstract

Streptococcus pneumoniae (Spn) is a common cause of respiratory infection, but also frequently colonizes the nasopharynx in the absence of disease. We used mass cytometry to study immune cells from nasal biopsy samples collected following experimental human pneumococcal challenge in order to identify immunological mechanisms of control of Spn colonization. Using 37 markers, we characterized 293 nasal immune cell clusters, of which 7 were associated with Spn colonization. B cell and CD8+CD161+ T cell clusters were significantly lower in colonized than in non-colonized subjects. By following a second cohort before and after pneumococcal challenge we observed that B cells were depleted from the nasal mucosa upon Spn colonization. This associated with an expansion of Spn polysaccharide-specific and total plasmablasts in blood. Moreover, increased responses of blood mucosal associated invariant T (MAIT) cells against in vitro stimulation with pneumococcus prior to challenge associated with protection against establishment of Spn colonization and with increased mucosal MAIT cell populations. These results implicate MAIT cells in the protection against pneumococcal colonization and demonstrate that colonization affects mucosal and circulating B cell populations

Type: Article
Title: Innate and adaptive nasal mucosal immune responses following experimental human pneumococcal colonization
Location: United States
Open access status: An open access version is available from UCL Discovery
DOI: 10.1172/JCI128865
Publisher version: https://doi.org/10.1172/JCI128865
Language: English
Additional information: This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
Keywords: B cells, Bacterial infections, Immunology, Infectious disease
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Div of Infection and Immunity
URI: https://discovery.ucl.ac.uk/id/eprint/10080968
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