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Resolution: standard / high Figure 3.
IL-33 deficiency does not reduce severity of arthritis induced by IgG purified from
K/BxN serum. (A) Incidence of arthritis induced by total IgG purified from K/BxN serum is shown for
WT C57BL/6 mice (n = 10, dashed line), IL-33 KO mice (n = 9, gray line), and ST2 KO mice (n = 10, black line). The incidence of arthritis was significantly retarded in ST2 KO,
as compared to WT or IL-33 KO mice (P < 0.01, longitudinal model for binomial data). Arthritis severity was evaluated by
clinical assessment of arthritis severity scores (B) and number of affected paws (C) in WT C57BL/6 mice (n = 10, dashed line), IL-33 KO mice (n = 9, gray line), and ST2 KO mice (n = 10, black line). Results shown represent the mean ± SEM for each group of mice.
The evolution of severity scores (B; P < 0.01, mixed model for repeated measures) and of the number of affected paws (C,
P < 0.001, longitudinal model for ordinal data) was significantly decreased in ST2 KO,
as compared to IL-33 KO and WT mice. In contrast, incidence and severity of arthritis
were similar in IL-33 KO and WT mice. IgG, immunoglobulin G; KO, knockout; WT, wild-type.
Martin et al. Arthritis Research & Therapy 2013 15:R13 doi:10.1186/ar4143 |