๐”– Bobbio Scriptorium
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NKT cells: facts, functions and fallacies

โœ Scribed by Dale I. Godfrey; Kirsten J.L. Hammond; Lynn D. Poulton; Mark J. Smyth; Alan G. Baxter


Publisher
Elsevier Science
Year
2000
Tongue
English
Weight
368 KB
Volume
21
Category
Article
ISSN
0167-5699

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โœฆ Synopsis


KT cells are a population of T cells that share some characteristics with natural killer (NK) cells (reviewed in Refs 1-3). The key features characteristic of NKT cells include heavily biased T-cell receptor (TCR) gene usage, CD1d restriction and high levels of cytokine production, particularly interleukin 4 (IL-4) and interferon โฅ (IFN-โฅ) (Fig. 1). In mice, these cells are commonly defined as NK1.1 ฯฉ โฃโคTCR ฯฉ . However, as cells bearing these markers are phenotypically and functionally heterogeneous, it is appropriate to compare the different subsets of cells encompassed within this population. Most of the studies covered in this review relate to NKT cells in mice, unless otherwise specified.

Subsets of NKT cells

Although the term NKT was only recently applied, these cells were first described in 1987. Most of the earlier studies in mice focussed on thymic โฃโคTCR ฯฉ T cells that were CD4 and CD8 double negative (โฃโคDN) and highly biased toward Vโค8-2 expression. A major subset of these cells was found to express NK1.1, previously associated with NK cells, and to have the potential to secrete high levels of IL-4, IFN-โฅ and tumor necrosis factor (TNF). A population of NK1.1 ฯฉ CD4 ฯฉ T cells was also identified with similar characteristics 1-3 . Subsequent reports showed that both populations predominantly express TCR Vโฃ14Jโฃ281 and that their development was dependent on the MHC class I-like, โค 2microglobulin-associated molecule, CD1d. These findings strongly suggested that NK1.1 ฯฉ โฃโคDN and NK1.1 ฯฉ CD4 ฯฉ T cells were part of the same lineage 1-3 . Thus, in recent years NKT cells are usually identified by the coexpression of the โฃโคTCR and NK1.1, as shown in Fig. 2.

Several recent studies in mice have demonstrated the potential danger of oversimplifying our classification of NKT cells [4][5][6][7][8] . These studies have shown that CD4 ฯฉ , DN and CD8 ฯฉ NK1.1 ฯฉ T cells are


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