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. 2019 May 30;14(5):e0217550. doi: 10.1371/journal.pone.0217550

Fig 6. Schematic diagram shows the basal immunophenotyping of axillary Th cells of non-IBC vs. IBC patients, and the immunoregulatory role of tumor Sdc-1 for CD4+ Th cell polarization of non-IBC patients.

Fig 6

(A) IBC patients are characterized by lower frequencies of circulating Th1 and Th2 subsets drained from axillary tributaries as compared to non-IBC patients. Relative to other Th subsets, Treg (CD4+Foxp3+) subset represents the lowest frequency among Th cells of non-IBC patients. (B) Upregulation of IL-23 and DLL4 expression mediated by Sdc-1 silencing in IBC cells may drive Th17 polarization under indirect and direct co-culture conditions. In addition, Sdc-1 silencing enhances Treg cell polarization under both indirect and direct co-culture conditions, whereas induces only Th1 polarization under indirect co-culture conditions.