Semaphorin4D Drives CD8+ T-Cell Lesional Trafficking in Oral Lichen Planus via CXCL9/CXCL10 Upregulations in Oral Keratinocytes

• DOI: 10.1016/j.jid.2017.07.818
• Publication Date: 2017-07-29T05:01:07Z
• Authors: Yao Ke; Erle Dang; Shengxian Shen; Tongmei Zhang; Hongjiang Qiao; Yuqian Chang; Qing Liu; Gang Wang
• Keywords: Keratinocytes; Administration, Topical; Biopsy, Needle; Semaphorins; CD8-Positive T-Lymphocytes; Triamcinolone; Chemokine CXCL9; Immunohistochemistry; Autoimmune Diseases; Up-Regulation; Chemokine CXCL10; 03 medical and health sciences; 0302 clinical medicine; Antigens, CD; Cell Movement; Case-Control Studies; Humans; RNA, Small Interfering; Cells, Cultured; Lichen Planus, Oral

Chemokine-mediated CD8+ T-cell recruitment is an essential but not well-established event for the persistence of oral lichen planus (OLP). Semaphorin 4D (Sema4D)/CD100 is implicated in immune dysfunction, chemokine modulation, and cell migration, which are critical aspects for OLP progression, but its implication in OLP pathogenesis has not been determined. In this study, we sought to explicate the effect of Sema4D on human oral keratinocytes and its capacity to drive CD8+ T-cell lesional trafficking via chemokine modulation. We found that upregulations of sSema4D in OLP tissues and blood were positively correlated with disease severity and activity. In vitro observation revealed that Sema4D induced C-X-C motif chemokine ligand 9/C-X-C motif chemokine ligand 10 production by binding to plexin-B1 via protein kinase B-NF-κB cascade in human oral keratinocytes, which elicited OLP CD8+ T-cell migration. We also confirmed using clinical samples that elevated C-X-C motif chemokine ligand 9/C-X-C motif chemokine ligand 10 levels were positively correlated with sSema4D levels in OLP lesions and serum. Notably, we determined matrix metalloproteinase-9 as a new proteolytic enzyme for the cleavage of sSema4D from the T-cell surface, which may contribute to the high levels of sSema4D in OLP lesions and serum. Our findings conclusively revealed an amplification feedback loop involving T cells, chemokines, and Sema4D-dependent signal that promotes OLP progression.