Dermatology and Pathology, Rutgers University New Jersey Medical School, Newark, NJ, USA.
J Eur Acad Dermatol Venereol. 2017 Nov;31(11):1817-1824. doi: 10.1111/jdv.14522. Epub 2017 Sep 14.
Langerhans cells (LCs) have been the subject of much research since their discovery in 1868. LCs belong to the subset of leucocytes called dendritic cells. They are present in the epidermis and the pilosebaceous apparatus and monitor the cutaneous environment for changes in homeostasis. During embryogenesis, a wave of yolk sac macrophages seed the fetal skin. Then, fetal liver monocytes largely replace the yolk sac macrophages and comprise the majority of adult LCs. In the presence of skin irritation, LCs process antigen and travel to regional lymph nodes to present antigen to reactive T lymphocytes. Changes in LCs' surface markers during the journey occur under the influence of cytokines. The difference in expression of surface markers and the ability to resist radiation have allowed researchers to differentiate LCs from the murine Langerin-positive dermal dendritic cells. Exciting discoveries have been made recently regarding their role in inflammatory skin diseases, cancer and HIV. New research has shown that antibodies blocking CD1a appear to mitigate inflammation in contact hypersensitivity reactions and psoriasis. While it has been established that LCs have the potential to induce effector cells of the adaptive immune system to counter oncogenesis, recent studies have demonstrated that LCs coordinate with natural killer cells to impair development of squamous cell carcinoma caused by chemical carcinogens. However, LCs may also physiologically suppress T cells and permit keratinocyte transformation and tumorigenesis. Although long known to play a primary role in the progression of HIV infection, it is now understood that LCs also possess the ability to restrict the progression of the disease. There is a pressing need to discover more about how these cells affect various aspects of health and disease; new information gathered thus far seems promising and exciting.
郎格汉斯细胞(LCs)自 1868 年发现以来一直是研究的热点。LCs 属于树突状细胞这一类白细胞。它们存在于表皮和毛囊皮脂腺中,监测皮肤环境中稳态的变化。在胚胎发生过程中,一波卵黄囊巨噬细胞定植于胎儿皮肤。然后,胎儿肝脏中的单核细胞大量取代卵黄囊巨噬细胞,成为成人 LCs 的主要来源。在皮肤受到刺激的情况下,LCs 处理抗原并迁移到局部淋巴结,向反应性 T 淋巴细胞呈递抗原。在细胞因子的影响下,LCs 表面标志物的变化发生。表面标志物表达的差异和对辐射的抵抗力使研究人员能够将 LCs 与鼠类 Langerin 阳性真皮树突状细胞区分开来。最近,人们对 LCs 在炎症性皮肤病、癌症和 HIV 中的作用有了令人兴奋的发现。新的研究表明,阻断 CD1a 的抗体似乎可以减轻接触性过敏反应和银屑病中的炎症。虽然已经确定 LCs 具有诱导适应性免疫系统效应细胞对抗肿瘤发生的潜力,但最近的研究表明,LCs 与自然杀伤细胞协调,以损害化学致癌剂引起的鳞状细胞癌的发展。然而,LCs 也可能在生理上抑制 T 细胞,允许角质形成细胞转化和肿瘤发生。尽管人们早就知道 LCs 在 HIV 感染的进展中起着主要作用,但现在人们明白,LCs 也具有限制疾病进展的能力。迫切需要更多地了解这些细胞如何影响健康和疾病的各个方面;迄今为止收集的新信息似乎很有希望和令人兴奋。