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. 2020 Aug 3;42(5):545–557. doi: 10.1007/s00281-020-00806-z

Table 1.

Immunosenescence features shared by the most common age-related diseases

Neurodegenerative diseases Rheumatoid arthritis Cancer Cardiovascular diseases Metabolic diseases References
Innate immunity
  Inflammaging [8, 25, 57, 66, 79, 99]
  Expansion of M1 macrophages [24, 57, 79, 94, 100, 101]
  Expansion of CD14++CD16+ monocytes [73, 102104]
  Expansion of myeloid-derived suppressor cells [105, 106]
Adaptive immunity
  Decreased thymic function [107]
  Contraction of T cell repertoire [108]
  Expansion in late-differentiated CD28 T cells [15, 28, 29, 52, 82]
  Expansion of TEMRA cells [17, 31]
  Expansion of regulatory T cells (FoxP3+) [54, 109]
  Increased CMV serology [52, 110113]
  Increased plasma autoantibodies [44, 114116]

Abbreviations: CMV, cytomegalovirus; FoxP3, forkhead box P3; TEMRA, effector memory T cells re-expressing CD45RA