HLA-E Peptide Repertoire and Dimorphism-Centerpieces in the Adaptive NK Cell Puzzle?

Front Immunol. 2018 Oct 17:9:2410. doi: 10.3389/fimmu.2018.02410. eCollection 2018.

Abstract

Adaptive Natural Killer (NK) cells, a heterogenous subpopulation of human NK cells with a unique phenotypic and functional signature, became arguably one of the central areas of interest in the field. While their existence seems closely associated with prior exposure to human cytomegalovirus (HCMV), many questions regarding their origin and regulation remain unanswered. However, a common denominator for the majority of adaptive NK cells is the expression of the activating heterodimeric receptor CD94/NKG2C that binds to HLA-E, a non-classical HLA molecule, that displays a comparably restricted expression pattern, very limited polymorphism and presents a distinct set of peptides. Recent studies suggest that-in analogy to T cell responses-peptides presented on HLA-E could play an unexpectedly decisive role for the biology of adaptive NK cells. Here, we discuss how this perspective on the CD94/NKG2C-HLA-E axis aligns with the existing literature and speculate about possible translational implication.

Keywords: FcεRγ; HLA-E; HLA-G; NKG2C; adaptive NK cells; leader peptide.

Publication types

  • Review

MeSH terms

  • Adaptive Immunity*
  • Animals
  • Cytomegalovirus / immunology
  • Cytomegalovirus Infections / immunology
  • Cytomegalovirus Infections / metabolism
  • Cytomegalovirus Infections / virology
  • Disease Susceptibility
  • Evolution, Molecular
  • HLA-E Antigens
  • Histocompatibility Antigens Class I / chemistry
  • Histocompatibility Antigens Class I / genetics
  • Histocompatibility Antigens Class I / immunology*
  • Host-Pathogen Interactions / genetics
  • Host-Pathogen Interactions / immunology
  • Humans
  • Immunotherapy
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / metabolism*
  • Lymphocyte Activation / genetics
  • Lymphocyte Activation / immunology
  • NK Cell Lectin-Like Receptor Subfamily C / metabolism
  • Neoplasms / etiology
  • Neoplasms / metabolism
  • Neoplasms / pathology
  • Neoplasms / therapy
  • Peptides / chemistry
  • Peptides / immunology*
  • Protein Binding

Substances

  • Histocompatibility Antigens Class I
  • KLRC1 protein, human
  • NK Cell Lectin-Like Receptor Subfamily C
  • Peptides