Laboratory of Rheumatology and Immunology, West China Hospital, Sichuan University, Chengdu 610041, China; Department of Rheumatology and Immunology, West China Hospital, Sichuan University, Chengdu 610041, China.
National Frontier Center of Disease Molecular Network, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610041, China.
EBioMedicine. 2022 Oct;84:104252. doi: 10.1016/j.ebiom.2022.104252. Epub 2022 Sep 9.
Primary Sjogren's syndrome (SS) is a chronic inflammatory disease with unknown aetiology. Although clonal expansion of autoreactive T cells has been identified in patients with SS, the clinical correlation of T-cell receptor (TCR) variance in SS remains unclear.
TCRβ repertoire sequencing was performed on 260 SS patients with 3-6 months of follow-up in a cohort study to dynamically assess the characteristics of TCR diversity and their clinical significance.
We found that SS patients had lower TCR diversity, but higher frequency of public clones than healthy controls (HCs). Significant differences were identified in the usage of the variable (V) gene, joining (J) gene, and V-J pairing between SS and HCs. Eighteen SS-associated clones were identified, showing a high sensitivity and specificity for disease classification. TCR diversity was correlated with the presence of dental caries, thrombocytopenia, hepatocholangeitis, antinuclear antibody, anti-SSA/SSB, and hypergammaglobulinemia but not with disease course, number of relapses, arthritis, rheumatoid factor, hypocomplementemia or disease activity defined by SSDAI. During follow-up, the TCR abnormalities remained, represented by more altered V/J usage and higher frequencies of SS-associated clones. Among SS patients, the sensitive subgroup had increased TCR diversity after treatment. Eighty-five SS-sensitivity associated TCRs were identified and used for sensitivity classification by cross validation with high specificity and sensitivity.
These results demonstrate that the TCR repertoire could provide insights into the disease status and prognosis in SS and other autoimmune diseases.
This study was funded by the National Key Research and Development Program of China (2016YFC0906201), Sichuan Science and Technology Program (2020YJ0223), and the 1·3·5 project for disciplines of excellence, West China Hospital, Sichuan University (ZYGD18015).
原发性干燥综合征(SS)是一种病因不明的慢性炎症性疾病。尽管在 SS 患者中已发现自身反应性 T 细胞的克隆扩增,但 SS 中 T 细胞受体(TCR)变异的临床相关性尚不清楚。
在一项队列研究中,对 260 例随访 3-6 个月的 SS 患者进行 TCRβ 谱测序,以动态评估 TCR 多样性特征及其临床意义。
我们发现 SS 患者的 TCR 多样性较低,但公共克隆的频率高于健康对照组(HCs)。SS 和 HCs 之间在 V 基因、J 基因的使用以及 V-J 配对方面存在显著差异。鉴定出 18 个与 SS 相关的克隆,对疾病分类具有较高的灵敏度和特异性。TCR 多样性与龋齿、血小板减少症、肝胆炎、抗核抗体、抗-SSA/SSB 和高丙种球蛋白血症有关,但与疾病病程、复发次数、关节炎、类风湿因子、低补体血症或 SSDAI 定义的疾病活动无关。在随访期间,TCR 异常仍然存在,表现为 V/J 使用改变更多,SS 相关克隆的频率更高。在 SS 患者中,敏感亚组在治疗后 TCR 多样性增加。通过交叉验证,确定了 85 个与 SS 敏感性相关的 TCR,并用于敏感性分类,具有较高的特异性和灵敏度。
这些结果表明,TCR 库可提供有关 SS 和其他自身免疫性疾病的疾病状态和预后的信息。
本研究得到了国家重点研发计划(2016YFC0906201)、四川省科技计划(2020YJ0223)和四川大学华西医院 1·3·5 学科卓越发展计划(ZYGD18015)的资助。