Vollmer S, Menssen A, Prinz J C
Department of Dermatology, Ludwig Maximilians-University, Munich, Germany.
J Invest Dermatol. 2001 Nov;117(5):1296-301. doi: 10.1046/j.0022-202x.2001.01494.x.
In a previous study we reported that clonally expanded T cell receptor beta-chain rearrangements characterized the T cell receptor usage in skin lesions of psoriasis vulgaris and indicated antigen-specific T cell selection. To assess the relevance of clonal T cell expansion for disease progression, we now determined if select clonal T cell receptor rearrangements persisted over time and were present in nonlesional skin. Sequential biopsies were taken from psoriatic skin lesions of two patients. V-D-J junctional regions of T cell receptor beta-chain variable region gene families 2, 3, 6, 13S1, and BV17 were cloned and sequenced, as these particular BV gene families are preferentially selected in psoriatic skin lesions. The lesional T cell receptor rearrangements were compared with the T cell receptor usage in nonlesional skin and in blood. Several T cell receptor beta-chain rearrangements with high transcript frequency in the first lesional biopsy were again found in sequential lesional biopsies taken as much as 3 y later from psoriasis relapses. Only T cell receptor beta-chain rearrangements with low transcript abundance showed variability in that several clones appeared for the first time or disappeared. Although nonlesional skin also exhibited a restricted T cell receptor usage with clonal T cell receptor rearrangements, the T cell receptor usage in lesional and nonlesional skin differed nearly completely. The select lesional recurrence of identical T cell receptor rearrangements reveals that inflammation in psoriasis involves the same clonally expanded T cell populations and the same antigens over prolonged periods of time. It hereby suggests that specifically recruited and locally expanded T cell clones are permanently involved in psoriatic inflammation and may play a crucial part in disease perpetuation.
在之前的一项研究中,我们报告称,克隆性扩增的T细胞受体β链重排可表征寻常型银屑病皮肤病变中的T细胞受体使用情况,并表明存在抗原特异性T细胞选择。为了评估克隆性T细胞扩增与疾病进展的相关性,我们现在确定特定的克隆性T细胞受体重排是否随时间持续存在以及是否存在于非病变皮肤中。对两名患者的银屑病皮肤病变进行了连续活检。克隆并测序了T细胞受体β链可变区基因家族2、3、6、13S1和BV17的V-D-J连接区,因为这些特定的BV基因家族在银屑病皮肤病变中被优先选择。将病变中的T细胞受体重排与非病变皮肤和血液中的T细胞受体使用情况进行了比较。在首次病变活检中具有高转录频率的几种T细胞受体β链重排,在多达3年后从银屑病复发时采集的连续病变活检中再次被发现。只有转录丰度低的T细胞受体β链重排表现出变异性,即几个克隆首次出现或消失。尽管非病变皮肤也表现出T细胞受体使用受限并伴有克隆性T细胞受体重排,但病变皮肤和非病变皮肤中的T细胞受体使用情况几乎完全不同。相同T细胞受体重排在病变中的选择性复发表明,银屑病中的炎症在很长一段时间内涉及相同的克隆性扩增T细胞群体和相同的抗原。由此表明,特异性募集和局部扩增的T细胞克隆长期参与银屑病炎症,并可能在疾病持续存在中起关键作用。