PD-1 Expression on NK Cells in Malaria-Exposed Individuals Is Associated with Diminished Natural Cytotoxicity and Enhanced Antibody-Dependent Cellular Cytotoxicity

Infect Immun. 2020 Feb 20;88(3):e00711-19. doi: 10.1128/IAI.00711-19. Print 2020 Feb 20.

Abstract

Natural killer (NK) cells are key effector cells of innate resistance capable of destroying tumors and virus-infected cells through cytotoxicity and rapid cytokine production. The control of NK cell responses is complex and only partially understood. PD-1 is an inhibitory receptor that regulates T cell function, but a role for PD-1 in regulating NK cell function is only beginning to emerge. Here, we investigated PD-1 expression on NK cells in children and adults in Mali in a longitudinal analysis before, during, and after infection with Plasmodium falciparum malaria. We found that NK cells transiently upregulate PD-1 expression and interleukin-6 (IL-6) production in some individuals during acute febrile malaria. Furthermore, the percentage of PD-1 expressing NK cells increases with age and cumulative malaria exposure. Consistent with this, NK cells of malaria-naive adults upregulated PD-1 following P. falciparum stimulation in vitro Additionally, functional in vitro studies revealed that PD-1 expression on NK cells is associated with diminished natural cytotoxicity but enhanced antibody-dependent cellular cytotoxicity (ADCC). These data indicate that PD-1+ NK cells expand in the context of chronic immune activation and suggest that PD-1 may contribute to skewing NK cells toward enhanced ADCC during infections such as malaria.

Keywords: NK cells; human immunology; malaria.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Adult
  • Age Factors
  • Animals
  • Antibody-Dependent Cell Cytotoxicity
  • CD56 Antigen / metabolism
  • Cell Line
  • Child
  • GPI-Linked Proteins / metabolism
  • Humans
  • Interleukin-6 / metabolism
  • K562 Cells
  • Killer Cells, Natural / immunology*
  • Longitudinal Studies
  • Malaria / immunology
  • Malaria, Falciparum / immunology*
  • Mice
  • Plasmodium falciparum / pathogenicity*
  • Programmed Cell Death 1 Receptor / metabolism*
  • Receptors, IgG / metabolism

Substances

  • CD56 Antigen
  • FCGR3B protein, human
  • GPI-Linked Proteins
  • IL6 protein, human
  • Interleukin-6
  • NCAM1 protein, human
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor
  • Receptors, IgG

Supplementary concepts

  • Acute malaria