
pmid: 21459674
Mucosal-associated invariant T (MAIT) cells are a population of T cells that display a semi-invariant T cell receptor (TCR) and are restricted by the evolutionarily conserved major histocompatibility complex related molecule, MR1. Here, we review recent knowledge of this T cell population. MAIT cells are abundant in human blood, gut and liver, and display an effector phenotype. They follow an atypical pathway of development and preferentially locate to peripheral tissues. Human and mouse MAIT cells react to bacterially infected cells in an MR1-dependent manner. They migrate to the infection site and can be protective in experimental infection models. MAIT cells secrete interferon-γ, and interleukin-17 under certain conditions. The species conservation, as well as the wide microbial reactivity, infer an important role for this cell population in immunity.
Mucous Membrane, Histocompatibility Antigens Class I, Interleukin-17, Receptors, Antigen, T-Cell, Bacterial Infections, Lymphocyte Activation, Minor Histocompatibility Antigens, Interferon-gamma, Mice, T-Lymphocyte Subsets, Animals, Humans
Mucous Membrane, Histocompatibility Antigens Class I, Interleukin-17, Receptors, Antigen, T-Cell, Bacterial Infections, Lymphocyte Activation, Minor Histocompatibility Antigens, Interferon-gamma, Mice, T-Lymphocyte Subsets, Animals, Humans
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 194 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 1% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 1% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 1% |
