Hansen E R, Baadsgaard O, Lisby S, Cooper K D, Thomsen K, Vejlsgaard G L
Department of Dermatology, Bispebjerg Hospital, Copenhagen, Denmark.
J Invest Dermatol. 1990 Apr;94(4):485-91. doi: 10.1111/1523-1747.ep12874650.
Cutaneous T-cell lymphoma is characterized by infiltration of the skin by activated CD4+ T lymphocytes. The mechanism by which these T lymphocytes achieve and maintain their activated state is unknown. Antigen-specific activation of T lymphocytes is dependent upon antigen-presenting cells which express HLA-DR class II major histocompatibility complex molecules, such as epidermal Langerhans cells. In addition to CD1+DR+ Langerhans cells, cutaneous T-cell lymphoma lesional epidermis contains major histocompatibility complex class II positive non-Langerhans cell populations, including CD1+OKM5+ bone-marrow-derived cells and DR+ keratinocytes. We asked whether any of these epidermal cell populations demonstrate capacity to activate T lymphocytes. Various numbers of epidermal cells from uninvolved and involved cutaneous T-cell lymphoma plaques were therefore used to stimulate autologous CD4+ and CD8+ T lymphocytes in the absence of exogenous antigen. Involved epidermal cells potently induced proliferation of CD4+ T lymphocytes (S.I. +/- SEM = 466 +/- 45). In contrast, uninvolved epidermal cells only induced background levels of proliferation (S.I. +/- SEM = 2 +/- 0.5, N = 8, p less than 0.01). Neither involved nor uninvolved epidermal cells were able directly to activate CD8+ lymphocytes. The capability of involved epidermal cells to activate CD4+ T lymphocytes was dependent upon CD1+DR+ leukocytes and not DR+ keratinocytes, because depletion of either HLA-DR+, CD1+ or HLe1+ epidermal cells totally abrogated the T-lymphocyte proliferation. Interestingly, on a cell per cell basis CD1+DR+ cells obtained from involved skin, demonstrated relative to CD1+DR+ cells from uninvolved skin, enhanced capacity to activate CD4+ T lymphocytes. Furthermore, CD1+OKM5+ cells from involved epidermis stimulated autologous CD4+ T lymphocytes. This indicates that a unique hitherto undescribed CD1+OKM5+ epidermal antigen-presenting cell population may participate in T-lymphocyte activation. These findings provide support for the concept that the epidermal cells in cutaneous T-cell lymphoma patients, particularly the antigen-presenting cells, may contribute significantly to the activation of CD4+ malignant and/or non-malignant inflammatory T lymphocytes within the skin.
皮肤T细胞淋巴瘤的特征是活化的CD4+ T淋巴细胞浸润皮肤。这些T淋巴细胞实现并维持其活化状态的机制尚不清楚。T淋巴细胞的抗原特异性活化依赖于表达HLA-DR II类主要组织相容性复合体分子的抗原呈递细胞,如表皮朗格汉斯细胞。除了CD1+DR+朗格汉斯细胞外,皮肤T细胞淋巴瘤病变表皮还含有主要组织相容性复合体II类阳性非朗格汉斯细胞群体,包括CD1+OKM5+骨髓来源细胞和DR+角质形成细胞。我们询问这些表皮细胞群体中是否有任何一种具有激活T淋巴细胞的能力。因此,在没有外源性抗原的情况下,使用来自未受累和受累皮肤T细胞淋巴瘤斑块的不同数量的表皮细胞来刺激自体CD4+和CD8+ T淋巴细胞。受累表皮细胞强烈诱导CD4+ T淋巴细胞增殖(刺激指数±标准误=466±45)。相比之下,未受累表皮细胞仅诱导背景水平的增殖(刺激指数±标准误=2±0.5,N = 8,p<0.01)。受累和未受累表皮细胞均不能直接激活CD8+淋巴细胞。受累表皮细胞激活CD4+ T淋巴细胞的能力依赖于CD1+DR+白细胞而非DR+角质形成细胞,因为HLA-DR+、CD1+或HLe1+表皮细胞的耗竭完全消除了T淋巴细胞增殖。有趣的是,就单个细胞而言,从受累皮肤获得的CD1+DR+细胞相对于从未受累皮肤获得的CD1+DR+细胞,具有增强的激活CD4+ T淋巴细胞的能力。此外,来自受累表皮的CD1+OKM5+细胞刺激自体CD4+ T淋巴细胞。这表明一种迄今未描述的独特的CD1+OKM5+表皮抗原呈递细胞群体可能参与T淋巴细胞激活。这些发现支持了这样一种观点,即皮肤T细胞淋巴瘤患者的表皮细胞,特别是抗原呈递细胞,可能对皮肤内CD4+恶性和/或非恶性炎性T淋巴细胞的激活有显著贡献。