Wollenberg Andreas, Wagner Moritz, Günther Sandra, Towarowski Andreas, Tuma Evelyn, Moderer Martina, Rothenfusser Simon, Wetzel Stefanie, Endres Stefan, Hartmann Gunther
Department of Dermatology and Allergy, University of Munich, Germany.
J Invest Dermatol. 2002 Nov;119(5):1096-102. doi: 10.1046/j.1523-1747.2002.19515.x.
Epidermal dendritic cells found in inflamed skin include Langerhans cells and the recently identified population of inflammatory dendritic epidermal cells. Another subset of dendritic cells in humans is the plasmacytoid dendritic cell in peripheral blood, which is characterized by the production of large amounts of type I interferon (interferon-alpha and interferon-beta) upon viral infection. We hypothesized that plasmacytoid dendritic cells might be involved in anti-viral defense mechanisms of the skin. Here we investigated plasmacytoid dendritic cells, inflammatory dendritic epidermal cells, and Langerhans cells in epidermal single cell suspensions of normal looking skin from healthy volunteers and of lesional skin from patients with different inflammatory skin diseases. Langerhans cells were found in normal and in inflamed skin samples. In normal skin, plasmacytoid dendritic cells and inflammatory dendritic epidermal cells were low or absent. Lesional skin samples from patients with psoriasis vulgaris and contact dermatitis contained relatively high numbers of both inflammatory dendritic epidermal cells and plasmacytoid dendritic cells. In contrast, many inflammatory dendritic epidermal cells but only very few plasmacytoid dendritic cells could be detected in atopic dermatitis lesions. Lupus erythematosus was characterized by high numbers of plasmacytoid dendritic cells but low numbers of inflammatory dendritic epidermal cells. These results demonstrate that in addition to resident Langerhans cells, plasmacytoid dendritic cells and inflammatory dendritic epidermal cells are selectively recruited to the skin lesions depending on the type of skin disease. The lack of plasmacytoid dendritic cells in atopic dermatitis may predispose atopic dermatitis patients to viral infections such as eczema herpeticum, a secondary infection of atopic dermatitis lesions with herpes simplex virus. The composition of dendritic cell subsets may help to clarify the etiology of inflammatory skin diseases and forms the basis for therapeutic intervention with selective microbial molecules such as immunostimulatory CpG oligonucleotides.
在炎症皮肤中发现的表皮树突状细胞包括朗格汉斯细胞和最近鉴定出的炎症性树突状表皮细胞群体。人类树突状细胞的另一个亚群是外周血中的浆细胞样树突状细胞,其特征是在病毒感染时产生大量I型干扰素(干扰素-α和干扰素-β)。我们推测浆细胞样树突状细胞可能参与皮肤的抗病毒防御机制。在此,我们研究了健康志愿者外观正常皮肤和不同炎症性皮肤病患者皮损处表皮单细胞悬液中的浆细胞样树突状细胞、炎症性树突状表皮细胞和朗格汉斯细胞。在正常皮肤和炎症皮肤样本中均发现了朗格汉斯细胞。在正常皮肤中,浆细胞样树突状细胞和炎症性树突状表皮细胞数量较少或不存在。寻常型银屑病和接触性皮炎患者的皮损样本中,炎症性树突状表皮细胞和浆细胞样树突状细胞数量相对较多。相比之下,在特应性皮炎皮损中可检测到许多炎症性树突状表皮细胞,但浆细胞样树突状细胞数量很少。红斑狼疮的特征是浆细胞样树突状细胞数量较多,但炎症性树突状表皮细胞数量较少。这些结果表明,除了常驻的朗格汉斯细胞外,浆细胞样树突状细胞和炎症性树突状表皮细胞会根据皮肤病的类型选择性地募集到皮肤病变部位。特应性皮炎中缺乏浆细胞样树突状细胞可能使特应性皮炎患者易患病毒感染,如疱疹样湿疹,即特应性皮炎皮损的单纯疱疹病毒继发感染。树突状细胞亚群的组成可能有助于阐明炎症性皮肤病的病因,并为使用免疫刺激性CpG寡核苷酸等选择性微生物分子进行治疗干预奠定基础。