Exp Dermatol. 2012 Mar;21(3):228-30. doi: 10.1111/j.1600-0625.2011.01437.x.
8-Methoxypsoralen plus UVA (PUVA) photochemotherapy is an effective treatment for many skin diseases including psoriasis. However, its exact mechanism of therapeutic action is incompletely understood. Previously, in K5.hTGFβ1 transgenic psoriatic mice, we found that PUVA induces Foxp3+ CD25+ CD4+ regulatory T cells in both lymph node and spleen. Now, in the same model, we investigated whether cutaneous lymphocyte-associated antigen (CLA) mediates PUVA's effect on homing of CD25+ CD4+ T cells to the lymph nodes of K5.hTGFβ1 transgenic mice. We found that a low dose of topical PUVA maximally increased the proportion of CLA + CD25+ CD4 + T cells in the lymph nodes by up to 8-fold. We also observed an increased number of Foxp3+ CD25+ T cells in the skin of the mice after PUVA treatment. Together, these findings suggest that PUVA affects the homing of regulatory T cells.
8-甲氧基补骨脂素加 UVA(PUVA)光化学疗法是治疗许多皮肤疾病的有效方法,包括银屑病。然而,其确切的治疗作用机制尚不完全清楚。先前,在 K5.hTGFβ1 转基因银屑病小鼠中,我们发现 PUVA 诱导淋巴结和脾脏中 Foxp3+ CD25+ CD4+调节性 T 细胞。现在,在相同的模型中,我们研究了皮肤淋巴细胞相关抗原(CLA)是否介导 PUVA 对 K5.hTGFβ1 转基因小鼠 CD25+ CD4+ T 细胞归巢到淋巴结的影响。我们发现,低剂量局部 PUVA 可将淋巴结中 CLA+ CD25+ CD4+T 细胞的比例最高增加 8 倍。我们还观察到 PUVA 治疗后小鼠皮肤中 Foxp3+ CD25+ T 细胞的数量增加。综上所述,这些发现表明 PUVA 影响调节性 T 细胞的归巢。