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. 2016 Apr 26;8(4):158–169. doi: 10.4252/wjsc.v8.i4.158

Table 3.

Mucosal-associated invariant T cells in the diseases

Category Mouse strains Disease model Phenotype Ref.
Bacterial infection MR1-/- Vα19 iTCR Tg Vβ6 Vβ8 Tg Escherichia coli Micobacterium abcessus Increase in the bacterial burden Repression of the bacterial burden [16]
MR1-/- Klebsiella pneumoniae Increased susceptibility to K. pneumoniae infection [36]
MR1-/- Mycobacterium bovis BCG Enhanced bacterial growth at the early stage of infection [35]
Francisella tularensis Delayed adaptive immune reaction [34]
Autoimmune diseases Vα19 iTCR Tg Experimental autoimmune encephalomyelitis (model of MS) Suppressed disease induction and progression [78]
MR1-/- Collagen-induced arthritis (model of rheumatoid arthritis) Improved CIA score [86]
Adoptive transfer Jα33+ MAIT cells into BALB/c TNBS induced colitis Improved disease index [105]
B10.RIII Spondyloarthropathy by IL-23 Enthesitis induced by IL-22 produced from IL-23R+RORγt+CD4-CD8- T cells (MAIT cells?) in the entheses [91]
Others Vα19 iTCR Tg NOD Non-obese diabetes Delayed disease onset [106]
Vα19 iTCR Tg Delayed-type hypersensitivity to sheep erythrocytes (type IV allergy) Suppression of the disease [106]

MAIT: Mucosal-associated invariant T; IL: Interleukin; CIA: Collagen-induced arthritis; iTCR: Invariant T cell receptor.