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. 2019 May 20;20(10):2487. doi: 10.3390/ijms20102487

Table 2.

Role of natural killer T cells in mouse models of systemic lupus erythematosus.

Strain (Model), Age Treatment Outcomes Ref.
NZB/NZW F1 (BWF1) mice None Expansion of NKT cells in association with the onset of the disease [30]
MRL/lpr mice, 2 months of age 6 μg of alpha-galactosylceramide (α-GalCer) twice a week for 5 months Improvement in inflammatory dermatitis without affecting renal disease [34]
BALB/c and SJL mice (pristane-induced) 6 μg of α-GalCer twice a week for 1 month Suppression of nephritis (BALB/c mice): exacerbation of nephritis (SJL mice) [35]
BWF1 young mice 0.5 mg of anti-NK1.1 antibody three times a week for long periods Amelioration of nephritis in late disease phase (worsening in early phase) [37]
BWF1 mice, 20 weeks of age 4 μg of α-GalCer twice a week for 2 weeks Enhancement of Th1 immune responses and exacerbation of nephritis [38]
BWF1 mice, 7 weeks of age 4 μg of α-GalCer twice at a 3-day interval Suppression of IL-10 production and reduction of severe proteinuria [39]
BWF1 mice, 24 weeks of age 2 μg of α-GalCer once a week for 4 weeks Suppression of Th2 immune responses and amelioration of nephritis [41]