| Literature DB >> 28119072 |
Elena Bianchini1, Sara De Biasi2, Anna Maria Simone3, Diana Ferraro3, Patrizia Sola3, Andrea Cossarizza4, Marcello Pinti1.
Abstract
Multiple sclerosis (MS) is a chronic progressive inflammatory demyelinating disorder of the central nervous system, and in several countries is a leading cause of permanent neurological disability in young adults, particularly women. MS is considered an autoimmune disease, caused by an aberrant immune response to environmental triggers in genetically susceptible subjects. However, the contribution of the innate or of the adaptive immune system to the development and progression of the disease has not yet been fully elucidated. Innate-like T lymphocytes are unconventional T cells that bridge the innate and adaptive arms of the immune system, because they use a T cell receptor to sense external ligands, but behave like innate cells when they rapidly respond to stimuli. These cells could play an important role in the pathogenesis of MS. Here, we focus on invariant natural killer T (iNKT) cells and mucosal-associated invariant T (MAIT) cells, and we review the current knowledge on their biology and possible involvement in MS. Although several studies have evaluated the frequency and functions of iNKT and MAIT cells both in MS patients and in experimental mouse models, contradictory observations have been reported, and it is not clear whether they exert a protective or a pro-inflammatory and harmful role. A better understanding of how immune cells are involved in MS, and of their interactions could be of great interest for the development of new therapeutic strategies.Entities:
Keywords: Innate-like T lymphocytes; Invariant natural killer T cells; Mucosal-associated invariant T cells; Multiple sclerosis
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Year: 2017 PMID: 28119072 DOI: 10.1016/j.imlet.2017.01.009
Source DB: PubMed Journal: Immunol Lett ISSN: 0165-2478 Impact factor: 3.685