Rapid NK cell differentiation in a population with near-universal human cytomegalovirus infection is attenuated by NKG2C deletions

Martin R. Goodier, Matthew J. White, Alansana Darboe, Carolyn M. Nielsen, Adriana Goncalves, Christian Bottomley, Sophie E. Moore, Eleanor M. Riley

Research output: Contribution to journalArticlepeer-review


Natural killer (NK) cells differentiate and mature during the human life course; human cytomegalovirus (HCMV) infection is a known driver of this process. We have explored human NK cell phenotypic and functional maturation in a rural African (Gambian) population with a high prevalence of HCMV. The effect of age on the frequency, absolute number, phenotype, and functional capacity of NK cells was monitored in 191 individuals aged from 1 to 49 years. Increasing frequencies of NK cells with age were associated with increased proportions of CD56(dim) cells expressing the differentiation marker CD57 and expansion of the NKG2C(+) subset. Frequencies of NK cells responding to exogenous cytokines declined with age in line with a decreased proportion of CD57(-) cells. These changes coincided with a highly significant drop in anti-HCMV IgG titers by the age of 10 years, suggesting that HCMV infection is brought under control as NK cells differentiate (or vice versa). Deletion at the NKG2Clocus was associated with a gene dose-dependent reduction in proportions of CD94(+) and CD57(+) NK cells. Importantly, anti-HCMV IgG titers were significantly elevated in NKG2C(-/-) children, suggesting that lack of expression of NKG2C may be associated with altered control of HCMV in childhood.

Original languageEnglish
Pages (from-to)2213-2222
Number of pages10
Issue number14
Early online date22 Aug 2014
Publication statusPublished - 2 Oct 2014


  • cd57 antigens
  • human herpesvirus 5
  • infections
  • natural killer cells
  • cd56 antigens
  • neural cell adhesion molecules
  • child
  • phenotype

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