Kapsenberg M L, Res P, Bos J D, Schootemijer A, Teunissen M B, Van Schooten W
Eur J Immunol. 1987 Jun;17(6):861-5. doi: 10.1002/eji.1830170620.
Inflammatory skin T cells were cloned in an antigen-independent way from lesions of patients with experimentally induced nickel-contact dermatitis. In three experiments 7-15% of the CD4+8- T lymphocyte clones (TLC) appeared to be specific for nickel in a proliferation assay. These proliferative response of nickel-specific TLC required the presence of antigen-presenting cells (APC) and were restricted by HLA class II molecules. All TLC recognized nickel presented by APC from epidermal skin. Remarkably, 5 out of 8 nickel-specific TLC exclusively recognized nickel when presented by these skin-specific APC whereas 3 out of these 8 clones could also recognize nickel presented by APC from peripheral blood. The critical APC within the fractions of epidermal cells and peripheral blood appeared to belong to the family of dendritic cells, i.e. Langerhans cells and circulating dendritic cells, respectively.
炎症性皮肤T细胞以抗原非依赖性方式从实验性诱导的镍接触性皮炎患者的皮损中克隆出来。在三项实验中,在增殖试验中7% - 15%的CD4 + 8 - T淋巴细胞克隆(TLC)似乎对镍具有特异性。这些镍特异性TLC的增殖反应需要抗原呈递细胞(APC)的存在,并且受HLA II类分子的限制。所有TLC均识别表皮皮肤来源的APC呈递的镍。值得注意的是,8个镍特异性TLC中有5个仅在由这些皮肤特异性APC呈递时才识别镍,而这8个克隆中有3个也能识别外周血来源的APC呈递的镍。表皮细胞和外周血组分中的关键APC似乎分别属于树突状细胞家族,即朗格汉斯细胞和循环树突状细胞。