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类风湿关节炎中T细胞受体库的分析。

Analysis of the T cell receptor repertoire in rheumatoid arthritis.

作者信息

Borgato L, Beri R, Biasi D, Testoni R, Cugola L, Cerù S, De Sandre G, Lunardi C

机构信息

Institute of Internal Medicine, University of Verona, Italy.

出版信息

Clin Exp Rheumatol. 1997 Sep-Oct;15(5):475-9.

PMID:9307853
Abstract

OBJECTIVE

To evaluate whether there is a restricted T cell receptor repertoire in rheumatoid synovium and to analyse the CDR3 region of the V beta families found to be more expressed in the synovial membrane than in the peripheral blood, in order to ascertain the presence of clonotypic expansion of T lymphocytes.

METHODS

The level of expression of individual V beta and V alpha families of the TCR was evaluated in paired synovial membrane and peripheral blood T cells from 8 female patients affected by rheumatoid arthritis, using the RT-PCR method. Nucleotide sequences of the CDR3 region of some V beta families were analysed in order to identify the presence of conserved sequences. Sequencing was carried out with the dideoxy chain termination method using modified T7 DNA polymerase.

RESULTS

All of the V alpha and V beta families were amplified in both compartments of the 8 patients. Four patients did not show any preferential expression of the TCR alpha or beta chains in synovium compared with peripheral blood. The other 4 patients showed increased expression of one or more V alpha and/or V beta families in the synovium. We did not find any correlation between the duration of disease, rheumatoid factor status, HLA-DR type and the V gene families which were elevated in the synovium. Analysis of the CDR3 region showed the presence of conserved amino acid sequences in the synovium, but not in the peripheral blood.

CONCLUSION

The V families found to be increased in 4 of the 8 patients studied were different, except for V beta 1 which was more highly expressed in 2 patients. The presence of conserved amino acid sequences in the CDR3 region is consistent with an antigen-driven T cell expansion at the site of autoimmune inflammation. These findings do not support our original hypothesis of the possible usefulness of therapy based on the inactivation or elimination of presumed pathogenic T cells using TCR-derived peptides or monoclonal antibodies against particular TCRs.

摘要

目的

评估类风湿性滑膜炎中是否存在受限的T细胞受体库,并分析在滑膜中比外周血中表达更高的Vβ家族的互补决定区3(CDR3)区域,以确定T淋巴细胞克隆型扩增的存在。

方法

使用逆转录聚合酶链反应(RT-PCR)方法,评估8例类风湿性关节炎女性患者配对的滑膜和外周血T细胞中TCR各个Vβ和Vα家族的表达水平。分析一些Vβ家族CDR3区域的核苷酸序列,以确定保守序列的存在。使用改良的T7 DNA聚合酶通过双脱氧链终止法进行测序。

结果

8例患者的两个部位均扩增出所有Vα和Vβ家族。4例患者的滑膜与外周血相比,未显示TCRα或β链有任何优先表达。其他4例患者的滑膜中一个或多个Vα和/或Vβ家族表达增加。我们未发现疾病持续时间、类风湿因子状态、HLA-DR类型与滑膜中升高的V基因家族之间存在任何相关性。CDR3区域分析显示滑膜中存在保守氨基酸序列,而外周血中没有。

结论

在研究的8例患者中的4例中发现V家族增加,除了Vβ1在2例患者中表达更高外,这些增加的V家族各不相同。CDR3区域中保守氨基酸序列的存在与自身免疫炎症部位抗原驱动的T细胞扩增一致。这些发现不支持我们最初的假设,即基于使用TCR衍生肽或针对特定TCR的单克隆抗体使假定的致病T细胞失活或消除的治疗可能有用。

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