Hiding lipid presentation: viral interference with CD1d-restricted invariant natural killer T (iNKT) cell activation

Viruses. 2012 Oct 23;4(10):2379-99. doi: 10.3390/v4102379.

Abstract

The immune system plays a major role in protecting the host against viral infection. Rapid initial protection is conveyed by innate immune cells, while adaptive immunity (including T lymphocytes) requires several days to develop, yet provides high specificity and long-lasting memory. Invariant natural killer T (iNKT) cells are an unusual subset of T lymphocytes, expressing a semi-invariant T cell receptor together with markers of the innate NK cell lineage. Activated iNKT cells can exert direct cytolysis and can rapidly release a variety of immune-polarizing cytokines, thereby regulating the ensuing adaptive immune response. iNKT cells recognize lipids in the context of the antigen-presenting molecule CD1d. Intriguingly, CD1d-restricted iNKT cells appear to play a critical role in anti-viral defense: increased susceptibility to disseminated viral infections is observed both in patients with iNKT cell deficiency as well as in CD1d- and iNKT cell-deficient mice. Moreover, viruses have recently been found to use sophisticated strategies to withstand iNKT cell-mediated elimination. This review focuses on CD1d-restricted lipid presentation and the strategies viruses deploy to subvert this pathway.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antigen Presentation
  • Antigens, CD1d / immunology*
  • HIV / immunology
  • HIV / pathogenicity
  • HIV Infections / immunology
  • HIV Infections / virology
  • Herpesviridae Infections / immunology
  • Herpesviridae Infections / virology
  • Herpesvirus 8, Human / immunology
  • Herpesvirus 8, Human / pathogenicity
  • Humans
  • Immune Evasion
  • Immunity, Innate
  • Lipids / immunology*
  • Lymphocyte Activation*
  • Mice
  • Natural Killer T-Cells / immunology
  • Natural Killer T-Cells / virology*
  • Viral Interference*

Substances

  • Antigens, CD1d
  • CD1D protein, human
  • Lipids