CD8+ T cell landscape in Indigenous and non-Indigenous people restricted by influenza mortality-associated HLA-A*24:02 allomorph.
Luca HensenPatricia T IllingE Bridie ClemensThi H O NguyenMarios KoutsakosCarolien E van de SandtNicole A MifsudAndrea T NguyenChristopher SzetoBrendon Y ChuaHanim HalimSimone RizzettoFabio LucianiLiyen LohEmma J GrantPhilippa M SaundersAndrew G BrooksSteve RockmanTom C KotsimbosAllen C ChengMichael RichardsGlen P WestallLinda M WakimThomas LoudovarisStuart I ManneringMichael ElliottStuart G TangyeDavid C JacksonKatie Louise FlanaganJamie RossjohnStephanie GrasJane DaviesAdrian MillerSteven Y C TongAnthony Wayne PurcellKatherine KedzierskaPublished in: Nature communications (2021)
Indigenous people worldwide are at high risk of developing severe influenza disease. HLA-A*24:02 allele, highly prevalent in Indigenous populations, is associated with influenza-induced mortality, although the basis for this association is unclear. Here, we define CD8+ T-cell immune landscapes against influenza A (IAV) and B (IBV) viruses in HLA-A*24:02-expressing Indigenous and non-Indigenous individuals, human tissues, influenza-infected patients and HLA-A*24:02-transgenic mice. We identify immunodominant protective CD8+ T-cell epitopes, one towards IAV and six towards IBV, with A24/PB2550-558-specific CD8+ T cells being cross-reactive between IAV and IBV. Memory CD8+ T cells towards these specificities are present in blood (CD27+CD45RA- phenotype) and tissues (CD103+CD69+ phenotype) of healthy individuals, and effector CD27-CD45RA-PD-1+CD38+CD8+ T cells in IAV/IBV patients. Our data show influenza-specific CD8+ T-cell responses in Indigenous Australians, and advocate for T-cell-mediated vaccines that target and boost the breadth of IAV/IBV-specific CD8+ T cells to protect high-risk HLA-A*24:02-expressing Indigenous and non-Indigenous populations from severe influenza disease.
Keyphrases
- gene expression
- end stage renal disease
- rheumatoid arthritis
- chronic kidney disease
- cardiovascular events
- ejection fraction
- cardiovascular disease
- risk factors
- oxidative stress
- dendritic cells
- machine learning
- newly diagnosed
- immune response
- high glucose
- risk assessment
- working memory
- coronary artery disease
- ankylosing spondylitis
- peritoneal dialysis
- deep learning
- diabetic rats
- wild type