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鉴定银屑病患者来源的表达Vbeta13和Vbeta15的浸润性T细胞常用的互补决定区3(CDR3)区域。

Identification of a commonly used CDR3 region of infiltrating T cells expressing Vbeta13 and Vbeta15 derived from psoriasis patients.

作者信息

Hwang Ha Young, Bahk Young Yil, Kim Tai-Gyu, Kim Tae-Yoon

机构信息

Laboratory of Dermatology-Immunology, Catholic Research Institute of Medical Science, College of Medicine, The Catholic University of Korea, Seoul, Korea.

出版信息

J Invest Dermatol. 2003 Mar;120(3):359-64. doi: 10.1046/j.1523-1747.2003.12055.x.

Abstract

Psoriasis is a common inflammatory skin disease that is thought to be mediated by activated T cells. In this study, the complementarity-determining region 3 (CDR3) in T cell receptors was examined for a common sequence motif among the T cells infiltrated in psoriatic lesional skin. A common specific CDR3 motif (Vbeta13-DWTSGV-Jbeta2.7) in lesions from psoriasis patients was identified by polymerase-chain-reaction-based spectratyping analysis and DNA sequencing. In addition, VDJ rearrangement with highly homologous amino acid composition in the CDR3 was observed in Vbeta15 of T cell receptors in lesions derived from psoriatic patients. Remarkably, T cell receptors containing the Vbeta13-DWTSGV-Jbeta2.7 were also found in the clinically normal skin from the psoriasis patients, which might seem to be responsible for the artificial production of psoriatic lesions. The identified CDR3 motif was highly expressed in cutaneous lymphocyte antigen (CLA+) cells of peripheral blood mononuclear cells from psoriasis patients compared with the expression in healthy individuals. This result showed that the infiltrated CLA+ T cells with the Vbeta13-DWTSGV-Jbeta2.7 motif in peripheral blood mononuclear cells from psoriasis patients might be involved in the development of psoriatic lesions. In addition, the results in this study suggest that the infiltrated T cells with the Vbeta13-DWTSGV-Jbeta2.7 motif in psoriatic lesions may be involved in the pathogenesis of psoriasis.

摘要

银屑病是一种常见的炎症性皮肤病,被认为是由活化的T细胞介导的。在本研究中,对银屑病皮损中浸润的T细胞的互补决定区3(CDR3)进行了检测,以寻找共同的序列基序。通过基于聚合酶链反应的谱型分析和DNA测序,在银屑病患者的皮损中鉴定出一种共同的特异性CDR3基序(Vbeta13-DWTSGV-Jbeta2.7)。此外,在银屑病患者皮损来源的T细胞受体Vbeta15中观察到CDR3氨基酸组成高度同源的VDJ重排。值得注意的是,在银屑病患者的临床正常皮肤中也发现了含有Vbeta13-DWTSGV-Jbeta2.7的T细胞受体,这可能是导致银屑病皮损人为产生的原因。与健康个体相比,银屑病患者外周血单核细胞的皮肤淋巴细胞抗原(CLA+)细胞中鉴定出的CDR3基序高度表达。这一结果表明,银屑病患者外周血单核细胞中带有Vbeta13-DWTSGV-Jbeta2.7基序的浸润CLA+ T细胞可能参与了银屑病皮损的发生发展。此外,本研究结果提示,银屑病皮损中带有Vbeta13-DWTSGV-Jbeta2.7基序的浸润T细胞可能参与了银屑病的发病机制。

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