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. 2022 Oct 2;13(5):S1–S26. doi: 10.1093/advances/nmac052

TABLE 2.

Summary of the key features of age-related immune decline (immunosenescence)1

Cell type Effect seen in immunosenescence
T lymphocyte
  • Decreased numbers in the circulation

  • Imbalances among different phenotypes (e.g., decreased ratio of CD4+ to CD8+ cells)

  • Decline in naive T-lymphocyte production and decreased numbers in the circulation

  • Accumulation of nonfunctional memory T lymphocytes

  • Diminished antigen receptor diversity

  • Impaired responsiveness

  • Impaired proliferation

  • Impaired production of cytokines (e.g., IL-2 and IFN-γ)

B lymphocytes
  • Decreased numbers of naive B lymphocytes in the circulation

  • Accumulation of nonfunctional memory B lymphocytes in the circulation

  • Impaired responsiveness

  • Altered balance of immunoglobulins

Dendritic cells
  • Decreased phagocytosis

  • Decreased TLR expression

  • Decreased responsiveness

  • Decreased type 1 IFN production

Neutrophils
  • Numbers in the circulation are preserved

  • Impaired chemotaxis

  • Impaired oxidative burst and bacterial killing

  • Impaired phagocytosis

  • Decreased TLR expression

  • Decreased production of neutrophil extracellular traps

  • Decreased responsiveness

Monocytes
  • Altered TLR expression

  • Decreased responsiveness

  • Altered pattern of cytokine production

Macrophages
  • Impaired phagocytosis

  • Altered TLR expression

  • Increased prostaglandin E2 production

NK cells
  • Increased numbers in the circulation

  • Imbalances among different phenotypes

  • Impaired cytotoxicity

  • Impaired responsiveness

1

TLR, Toll-like receptor.