We evaluated the expression of T cell–restricted intracellular antigen (Tia-1), granzyme B, and perforin by lymphocytes and the degree of epithelial apoptosis in oral and cutaneous lichen planus (LP) in 51 untreated cases, including 27 oral LP (OLP) and 24 cutaneous LP (CLP) cases. The number of total dermal-positive lymphocytes in OLP and CLP was similar, indicating similar activity of the inflammatory process. Intraepithelial Tia-1–positive, perforin-positive, and granzyme B–positive lymphoid cells were more numerous in OLP than in CLP (P < .05). The epithelial cell apoptotic index (AI) was increased significantly in OLP (P < .05), particularly in erosive-atrophic variants. A linear correlation between AI and the mean ± SEM number of intraepithelial and dermal perforin+ cells (6.85 ± 2.44 and 27.48 ± 10.19, respectively), per 10 high-power fields for OLP and for CLP (1.17 ± 0.88 and 10.42 ± 5.74, respectively), was found (intraepithelial, r = 0.50; dermal, r = 0.51; P < .01). These data suggest a pivotal role for perforin in triggering epithelial cell apoptosis. The differences of infiltrating cytotoxic cells and related AI observed in OLP and CLP are in keeping with the clinical behaviors that distinguish these LP variants.

Cytotoxic molecule expression and epithelial cell apoptosis in oral and cutaneous lichen planus

MAJORANA, Alessandra;BARDELLINI, Elena;SAPELLI, Pierluigi;FACCHETTI, Fabio
2004-01-01

Abstract

We evaluated the expression of T cell–restricted intracellular antigen (Tia-1), granzyme B, and perforin by lymphocytes and the degree of epithelial apoptosis in oral and cutaneous lichen planus (LP) in 51 untreated cases, including 27 oral LP (OLP) and 24 cutaneous LP (CLP) cases. The number of total dermal-positive lymphocytes in OLP and CLP was similar, indicating similar activity of the inflammatory process. Intraepithelial Tia-1–positive, perforin-positive, and granzyme B–positive lymphoid cells were more numerous in OLP than in CLP (P < .05). The epithelial cell apoptotic index (AI) was increased significantly in OLP (P < .05), particularly in erosive-atrophic variants. A linear correlation between AI and the mean ± SEM number of intraepithelial and dermal perforin+ cells (6.85 ± 2.44 and 27.48 ± 10.19, respectively), per 10 high-power fields for OLP and for CLP (1.17 ± 0.88 and 10.42 ± 5.74, respectively), was found (intraepithelial, r = 0.50; dermal, r = 0.51; P < .01). These data suggest a pivotal role for perforin in triggering epithelial cell apoptosis. The differences of infiltrating cytotoxic cells and related AI observed in OLP and CLP are in keeping with the clinical behaviors that distinguish these LP variants.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11379/28761
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