Therapeutic manipulation of natural killer (NK) T cells in autoimmunity: are we close to reality?
Author(s) -
Simoni Y.,
Diana J.,
Ghazarian L.,
Beaudoin L.,
Lehuen A.
Publication year - 2013
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/j.1365-2249.2012.04625.x
Subject(s) - immunology , autoimmunity , major histocompatibility complex , natural killer t cell , population , biology , primary biliary cirrhosis , innate lymphoid cell , t cell , innate immune system , immune system , medicine , environmental health
Summary T cells reactive to lipids and restricted by major histocompatibility complex (MHC) class I‐like molecules represent more than 15% of all lymphocytes in human blood. This heterogeneous population of innate cells includes the invariant natural killer T cells (iNK T), type II NK T cells, CD1a,b,c‐restricted T cells and mucosal‐associated invariant T (MAIT) cells. These populations are implicated in cancer, infection and autoimmunity. In this review, we focus on the role of these cells in autoimmunity. We summarize data obtained in humans and preclinical models of autoimmune diseases such as primary biliary cirrhosis, type 1 diabetes, multiple sclerosis, systemic lupus erythematosus, rheumatoid arthritis, psoriasis and atherosclerosis. We also discuss the promise of NK T cell manipulations: restoration of function, specific activation, depletion and the relevance of these treatments to human autoimmune diseases.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom