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Fig. 4 | Arthritis Research & Therapy

Fig. 4

From: Modulating IL-21-driven B cell responses in idiopathic inflammatory myopathies via inhibition of the JAK/STAT pathway

Fig. 4

Tofacitinib treatment of PBMC from DM, ASyS and OM significantly reduces B cell proliferation, but mainly affects their differentiation and antibody production in a 6-day culture. (A) Histograms show the percentage of proliferation based on CFSE staining from a representative ASyS patient within CD19+CD20+ B cells. Graphs include analysis from all samples. (B) Percentage of CD27+CD38+ plasmablasts (of CD19+CD20+ B cells) and of CD138+ PC (of CD3- cells). (C) Representative dot plots and analysis of the percentage of naive and memory populations (within CD19+CD20+ B cells): switched memory (SWM) (CD27+IgD-), non-switched memory (NSM) (CD27+IgD+), naive (CD27-IgD+) and double negative (DN) (CD27-IgD-). (D) Analysis of the IgG, IgM and IgA levels in the culture supernatants. DM: dermatomyositis, ASyS: anti-synthetase syndrome, OM: overlap myositis. Tofa: tofacitinib (2.5 µM). Graphs show the mean, SD and individual values (**p < 0.01; ***p < 0.001, n = 4/IIM subgroup)

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