Komatsu T, Moriya N, Shiohara T
Department of Dermatology, Kyorin University School of Medicine, Tokyo, Japan.
Clin Exp Immunol. 1996 May;104(2):343-50. doi: 10.1046/j.1365-2249.1996.30738.x.
Human epidermis contains a phenotypically heterogeneous population of T cells. No information however, is available regarding the TCR repertoire of these T cells and their relevant physiologic and pathologic functions in vivo. To this end, T cells were prepared from the lesional epidermis in two patients with fixed drug eruption (FDE) and their phenotype, function and TCR repertoire were examined in parallel. Both epidermal T cells, termed FDE-1 and -2 cells, respectively, expressed alpha beta TCR, but displayed some phenotypic heterogeneity. These T cells were induced to display cytolytic activity by ligation of the CD3/TCR-alpha beta complex. Comparative analyses of TCR V alpha and V beta expression in the epidermal T cells and the paired peripheral blood lymphocytes (PBL) by quantitative polymerase chain reaction (PCR) demonstrated that the epidermal T cells, but not the paired PBL, utilized a very limited range of V alpha and V beta genes. These results indicate that some expansion or preferential migration of epidermal T cells that recognize a restricted set of antigens expressed within the epidermis could occur in situ following ingestion of the causative drug. The persistence of these epidermal T cells in FDE lesions suggests their pathologic role in a drug-induced flare.
人类表皮含有表型异质性的T细胞群体。然而,关于这些T细胞的TCR库及其在体内相关的生理和病理功能,目前尚无相关信息。为此,从两名固定性药疹(FDE)患者的皮损表皮中制备T细胞,并同时检测其表型、功能和TCR库。这两种表皮T细胞分别称为FDE-1和FDE-2细胞,均表达αβ TCR,但表现出一定的表型异质性。通过CD3/TCR-αβ复合物的连接诱导这些T细胞表现出细胞溶解活性。通过定量聚合酶链反应(PCR)对表皮T细胞和配对的外周血淋巴细胞(PBL)中的TCR Vα和Vβ表达进行比较分析,结果表明,表皮T细胞而非配对的PBL利用了非常有限的Vα和Vβ基因范围。这些结果表明,摄入致病药物后,在表皮内识别一组受限抗原的表皮T细胞可能会在原位发生一些扩增或优先迁移。这些表皮T细胞在FDE皮损中的持续存在表明它们在药物诱发的皮疹中起病理作用。