Fig. 6From: Normal ex vivo mesenchymal stem cell function combined with abnormal immune profiles sets the stage for informative cell therapy trials in idiopathic pulmonary fibrosis patientsImmnunoprofile comparison of blood samples from IPF patients and HCs using unpaired Student's t test. A. B cells panel. There is no difference in total B cell numbers between the tested groups. IPF patients have decreased percentage as well as cell number of [IgD + IgM +] cells, smaller percentage of transitional B cells, while higher percentage of [IgD-IgM-] cells. B. Granulocytes, eosinophils and neutrophils panel. IPF patients have elevated numbers of granulocytes, eosinophils as well as neutrophils than HCs. C. T cells panel: Total number of T (CD3 +) cells is not different between two groups, while the percentages of [CD4 + CTLA4 +], CD4 + CTLA4 + CD28 +], [C8 + CTLA4 +], [C8 + CTLA4 + CD28 +], [CD8 + PD-1 +] cells as well as [CD25 + Treg] and [CD4 + Tcm] T cells are elevated. Only the percentage CD25 + CD45RA + Treg cells is decreased. D. Monocytes panel: The monocyte phenotype showed higher percentage in IPF patients. Dots represent each individual values. *p < 0.05, **p < 0.01, ***p < 0.001, ***p < 0.0001, compared with control groupBack to article page