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Single-cell transcriptomics reveals expansion of cytotoxic CD4 T cells in supercentenarians.

Kosuke HashimotoTsukasa KounoTomokatsu IkawaNorihito HayatsuYurina MiyajimaHaruka YabukamiTommy TerooateaTakashi SasakiTakahiro SuzukiMatthew ValentineGiovanni PascarellaYasushi OkazakiHarukazu SuzukiJay W ShinAki MinodaIchiro TaniuchiHideyuki OkanoYasumichi AraiNobuyoshi HirosePiero Carnici
Published in: Proceedings of the National Academy of Sciences of the United States of America (2019)
Supercentenarians, people who have reached 110 y of age, are a great model of healthy aging. Their characteristics of delayed onset of age-related diseases and compression of morbidity imply that their immune system remains functional. Here we performed single-cell transcriptome analysis of 61,202 peripheral blood mononuclear cells (PBMCs), derived from 7 supercentenarians and 5 younger controls. We identified a marked increase of cytotoxic CD4 T cells (CD4 cytotoxic T lymphocytes [CTLs]) as a signature of supercentenarians. Furthermore, single-cell T cell receptor sequencing of 2 supercentenarians revealed that CD4 CTLs had accumulated through massive clonal expansion, with the most frequent clonotypes accounting for 15 to 35% of the entire CD4 T cell population. The CD4 CTLs exhibited substantial heterogeneity in their degree of cytotoxicity as well as a nearly identical transcriptome to that of CD8 CTLs. This indicates that CD4 CTLs utilize the transcriptional program of the CD8 lineage while retaining CD4 expression. Indeed, CD4 CTLs extracted from supercentenarians produced IFN-γ and TNF-α upon ex vivo stimulation. Our study reveals that supercentenarians have unique characteristics in their circulating lymphocytes, which may represent an essential adaptation to achieve exceptional longevity by sustaining immune responses to infections and diseases.
Keyphrases
  • single cell
  • rna seq
  • immune response
  • nk cells
  • gene expression
  • rheumatoid arthritis
  • poor prognosis
  • genome wide
  • inflammatory response
  • quality improvement
  • long non coding rna
  • dna methylation
  • cell fate