Natural killer T cell

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Arcadian (talk | contribs) at 03:05, 6 October 2006 (added image). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Natural killer cell

Natural killer T (NKT) cells are a heterogeneous group of T cells that share properties of both T cells and natural killer (NK) cells. Many of these cells recognize the non-polymorphic CD1d molecule, an antigen-presenting molecule that binds self- and foreign lipids and glycolipids. They constitute only 0.2% of all peripherial blood T cells.[1]

Nomenclature

The term “NK T cells” was first used in mice to define a subset of T cells that expressed the natural killer (NK) cell-associated marker NK1.1 (CD161). It is now generally accepted that the term “NKT cells” refers to CD1d-restricted T cells, present in mice and humans, coexpressing a heavily biased, semi-invariant T cell receptor (TCR) and NK cell markers.[2] Natural killer T (NKT) cells should not be confused with natural killer (NK) cells.

Molecular Characterization

NKT cells are a subset of T cells that co-express an αβ T cell receptor (TCR), but also express a variety of molecular markers that are typically associated with NK cells, such as NK1.1. They differ from conventional αβ T cells in that their TCRs are far more limited in diversity and in that they recognize lipids and glycolipids presented by CD1d molecules, a member of the CD1 family of antigen presenting molecules, rather than peptide-MHC complexes. NKT cells include both NK1.1+ and NK1.1-, as well as CD4+, CD4-, CD8+ and CD8- cells. Natural Killer T cells share other features with NK cells as well, such as CD16 and CD56 expression and granzyme production.[3][4]

Classification

Classification of natural killer T cells into three groups has been proposed.[2]

Type 1 NKT Type 2 NKT NKT-Like
Other names classical NKT
invariant NKT (iNKT)
Vα14i NKT (mouse)
Vα24i NKT (human)
non-classical NKT
diverse NKT
NK1.1+ T cells
CD3+ CD56+ T cells
Restriction CD1d CD1d MHC, other?
α-GalCer
reactivity
+ - -
TCR repetoire Vα14-Jα18:
Vβ8.2, 7, 2 (mouse)
Vα24-Jα18:
Vβ11 (human)
diverse diverse

iNKT cells

The best known subset of CD1d-dependent NKT cells expresses an invariant T cell receptor α (TCR-α) chain. These are referred to as type I or invariant NKT cells (iNKT) cells.These cells are conserved between humans and mice and are implicated in many immunological processes.

Function

Upon activation, NK T cells are able to produce large quantities of interferon-gamma, IL-4, and granulocyte-macrophage colony-stimulating factor, as well as multiple other cytokines and chemokines (such as IL-2 and TNF-alpha).

Significance

NKT cells seem to be essential for several aspects of immunity because their dysfunction or deficiency leads to a development of autoimmune diseases (such as diabetes or atherosclerosis) and cancers. NKT cells have recently been implicated in the disease progression of human asthma.

Their clinical potential lies in the rapid release of cytokines (such as IL-2, IFN-gamma, TNF-alpha, and IL-4) that promote or suppress different immune responses, which has earned NKT cells the moniker of the ‘double-edged sword’ of the immune system.

References

  1. ^ Jerud, ES (2006). "Natural Killer T cells: Roles in Tumor Immunosurveillance and Tolerance". Transfus. Med. Hemother. 33: 18–36. {{cite journal}}: Unknown parameter |coauthor= ignored (|author= suggested) (help)
  2. ^ a b Godfrey, DI (2004). "NKT cells: what's in a name?". Nat. Rev. Immunol. 4: 231. {{cite journal}}: Unknown parameter |coauthor= ignored (|author= suggested) (help)
  3. ^ Van der Vliet, HJ (1999). "Effects of alphagalactosylceramide (KRN7000), interleukin-12 and interleukin-7 on phenotype and cytokine profile of human V24+ V11+ T cells". Immunology. 98: 557–563. {{cite journal}}: Unknown parameter |coauthor= ignored (|author= suggested) (help)
  4. ^ Vivier, E (2004). "Inhibitory NK-cell receptors on T cells. Witness of the past, actors of the future". Nat Rev Immunol. 4: 190–198. {{cite journal}}: Unknown parameter |coauthor= ignored (|author= suggested) (help); line feed character in |title= at position 29 (help)