Changes in Mycobacterium tuberculosis-Specific Immunity With Influenza co-infection at Time of TB Diagnosis

Prior Influenza A viral (IAV) infection has been shown to increase susceptibility to tuberculosis (TB) and TB has also been shown to be a primary cause of death during pandemics, including the Spanish Influenza outbreak of 1918-1919. The majority of data has been obtained from mouse models, thus the...

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Published inFrontiers in immunology Vol. 9; p. 3093
Main Authors Mendy, Joseph, Jarju, Sheikh, Heslop, Rhiannon, Bojang, Adama L., Kampmann, Beate, Sutherland, Jayne S.
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 04.01.2019
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Summary:Prior Influenza A viral (IAV) infection has been shown to increase susceptibility to tuberculosis (TB) and TB has also been shown to be a primary cause of death during pandemics, including the Spanish Influenza outbreak of 1918-1919. The majority of data has been obtained from mouse models, thus the aim of this study was to determine the impact of Flu co-infection on host immunity and disease severity in TB patients at diagnosis. Sputum from 282 patients with active TB were analyzed for presence of FluA/FluB RNA at presentation using multiplex PCR. Sputum RNA was also analyzed for (Mtb) load using S RNA amplification. Supernatants from digested sputum and Mtb antigen-stimulated whole blood were analyzed using multiplex cytokine arrays and PBMC were analyzed for cytokine production from CD4+ T, CD8+ T and Mucosal Associated Invariant T cells (MAITs). 12 (4.3%) of TB patients were found to have FluA or FluB viral RNA present in their sputum at the time of TB diagnosis. The TB/Flu co-infected patients had a significantly higher bacterial load compared to those with TB mono-infection ( = 0.0026). They had lower levels of IL17A in sputum ( = 0.0275) and higher MCP-1 (CCL2) levels in the blood following PPD stimulation ( = 0.0267). TB/Flu co-infected subjects had significantly higher IFN-γ+IL-17+CD4+ and IFN-γ+IL-17-CD8+ cells compared to TB mono-infected subjects. These data show that Flu co-infection at time of TB diagnosis is associated with a higher bacterial load and differential cellular and soluble profiles. These findings show for the first time the impact of TB/Flu co-infection in a human cohort and support the potential benefit of Flu vaccination in TB-endemic settings.
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This article was submitted to Microbial Immunology, a section of the journal Frontiers in Immunology
Edited by: Christoph Hölscher, Forschungszentrum Borstel (LG), Germany
Reviewed by: Bianca Schneider, Forschungszentrum Borstel (LG), Germany; Warwick Britton, University of Sydney, Australia
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2018.03093