Evidence of immunometabolic dysregulation and airway dysbiosis in athletes susceptible to respiratory illness

Background: Respiratory tract infection (RTI) is a leading cause of training and in-competition time-loss in athlete health. The immune factors associated with RTI susceptibility remain unclear. In this study, we prospectively characterise host immune factors in elite athletes exhibiting RTI suscept...

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Main Authors: Cookson, W.O.C (Author), Cuthbertson, L. (Author), Hull, J.H (Author), Jackson, A. (Author), Kelleher, P. (Author), Loosemore, M. (Author), Moffatt, M.F (Author), Ranson, C. (Author), Shah, A. (Author), Turner, S.E.G (Author)
Format: Article
Language:English
Published: Elsevier B.V. 2022
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Online Access:View Fulltext in Publisher
LEADER 02884nam a2200301Ia 4500
001 10.1016-j.ebiom.2022.104024
008 220706s2022 CNT 000 0 und d
020 |a 23523964 (ISSN) 
245 1 0 |a Evidence of immunometabolic dysregulation and airway dysbiosis in athletes susceptible to respiratory illness 
260 0 |b Elsevier B.V.  |c 2022 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1016/j.ebiom.2022.104024 
520 3 |a Background: Respiratory tract infection (RTI) is a leading cause of training and in-competition time-loss in athlete health. The immune factors associated with RTI susceptibility remain unclear. In this study, we prospectively characterise host immune factors in elite athletes exhibiting RTI susceptibility. Methods: Peripheral blood lymphocyte flow cytometry phenotyping and 16S rRNA microbial sequencing of oropharyngeal swabs was performed in a prospective elite athlete cohort study (n = 121). Mass cytometry, peripheral blood mononuclear cell (PBMC) stimulation and plasma metabolic profiling was performed in age-matched highly-susceptible (HS) athletes (≥4RTI in last 18 months) (n = 22) compared to non-susceptible (NS) (≤1RTI in last 18 months) (n = 23) athletes. Findings were compared to non-athletic healthy controls (HC) (n = 19). Findings: Athletes (n = 121) had a reduced peripheral blood memory T regulatory cell compartment compared to HC (p = 0.02 (95%CI:0.1,1.0)) and reduced upper airway bacterial biomass compared to HC (p = 0.032, effect size r = 0.19). HS athletes (n = 22) had lower circulating memory T regulatory cells compared to NS (n = 23) athletes (p = 0.005 (95%CI:-1.5,-0.15)) and HC (p = 0.002 (95%CI:-1.9,-0.3) with PBMC microbial stimulation assays revealing a T-helper 2 skewed immune response compared to HC. Plasma metabolomic profiling showed differences in sphingolipid pathway metabolites (a class of lipids important in infection and inflammation regulation) in HS compared to NS athletes and HC, with sphingomyelin predictive of RTI infection susceptibility (p = 0.005). Interpretation: Athletes susceptible to RTI have reduced circulating memory T regulatory cells, metabolic dysregulation of the sphingolipid pathway and evidence of upper airway bacterial dysbiosis. Funding: This study was funded by the English Institute of Sport (UK). © 2022 The Authors 
650 0 4 |a Exercise 
650 0 4 |a Microbiome 
650 0 4 |a Respiratory tract infection 
650 0 4 |a Sphingolipid 
650 0 4 |a T regulatory cell 
700 1 0 |a Cookson, W.O.C.  |e author 
700 1 0 |a Cuthbertson, L.  |e author 
700 1 0 |a Hull, J.H.  |e author 
700 1 0 |a Jackson, A.  |e author 
700 1 0 |a Kelleher, P.  |e author 
700 1 0 |a Loosemore, M.  |e author 
700 1 0 |a Moffatt, M.F.  |e author 
700 1 0 |a Ranson, C.  |e author 
700 1 0 |a Shah, A.  |e author 
700 1 0 |a Turner, S.E.G.  |e author 
773 |t eBioMedicine