Xu Jingyi, Si Shucheng, Han Yijun, Zeng Lin, Zhao Jinxia
Department of Rheumatology and Immunology, Peking University Third Hospital, No. 49, North Garden Road, Beijing, 100191, China.
Research Center of Clinical Epidemiology, Peking University Third Hospital, No. 49, North Garden Road, Beijing, 100191, China.
J Transl Med. 2025 Jan 13;23(1):56. doi: 10.1186/s12967-024-05993-z.
Sjogren syndrome (SS) is a chronic systemic autoimmune disease and its pathogenesis often involves the participation of numerous immune cells and inflammatory factors. Despite increased researches and studies recently focusing on this area, it remains to be fully elucidated. We decide to incorporate genetic insight into investigation of the causal link between various immune cells, inflammatory factors and pathogenesis of Sjogren syndrome (SS).
Our study leveraged the genetic variants of multi-omics statistics extracted from genome-wide association study (GWAS), the University of Bristol and the FinnGen study. We performed a bidirectional Mendelian randomization and mediation study based on randomly allocated instrumental variables to infer causality, followed by external validation with UK Biobank data and Bayesian colocalization.
We demonstrated that an elevated level of CD27 on IgD + CD24 + B cell, a subset of B cells expressing both IgD and CD24, was associated with a higher risk of SS (OR = 1.119, 95% CI: 1.061-1.179, P < 0.001), while CD3 on CD45RA + CD4 + Treg was a protective factor (OR = 0.917, 95%CI: 0.877-0.959, P < 0.001). Results of meta-analysis and colocalization further supported the significant results identified in the primary analysis. A total of 4 inflammatory cytokines and 7 circulating proteins exhibited potential causal relationships with SS despite no significant result achieved after FDR correction. Finally, results of mediation analysis indicated that CD40L receptor levels had significant mediating effects (β = 0.0314, 95% CI: 0.0004-0.0624, P = 0.0471) at a mediation proportion of 28% (95% CI: 0.364%-55.6%) in causal relationship between CD27 on IgD + CD24 + B cell and SS.
By providing a novel genetic insight into unveiling the roles of autoimmunity and inflammation in Sjogren syndrome, our findings may potentially lead to identifying new clinical biomarkers for disease monitoring and therapeutic targets that offer more effective alternatives for treating this condition. Therefore, our study may provide valuable evidence for future clinical intervention and targeted immunotherapy.
干燥综合征(SS)是一种慢性全身性自身免疫性疾病,其发病机制通常涉及众多免疫细胞和炎症因子的参与。尽管最近对该领域的研究有所增加,但仍有待充分阐明。我们决定将遗传学见解纳入对各种免疫细胞、炎症因子与干燥综合征(SS)发病机制之间因果关系的研究。
我们的研究利用了从全基因组关联研究(GWAS)、布里斯托大学和芬兰基因研究中提取的多组学统计的遗传变异。我们基于随机分配的工具变量进行了双向孟德尔随机化和中介研究以推断因果关系,随后用英国生物银行数据和贝叶斯共定位进行外部验证。
我们证明,IgD⁺CD24⁺B细胞(同时表达IgD和CD24的B细胞亚群)上CD27水平升高与SS风险较高相关(OR = 1.119,95%CI:1.061 - 1.179,P < 0.001),而CD45RA⁺CD4⁺调节性T细胞(Treg)上的CD3是一个保护因素(OR = 0.917,95%CI:0.877 - 0.959,P < 0.001)。荟萃分析和共定位结果进一步支持了在初步分析中确定的显著结果。尽管在错误发现率(FDR)校正后未获得显著结果,但共有4种炎性细胞因子和7种循环蛋白与SS表现出潜在因果关系。最后,中介分析结果表明,在IgD⁺CD24⁺B细胞上的CD27与SS的因果关系中,CD40L受体水平具有显著中介作用(β = 0.0314,95%CI:0.0004 - 0.0624,P = 0.0471),中介比例为28%(95%CI:0.364% - 55.6%)。
通过提供一种新的遗传学见解来揭示自身免疫和炎症在干燥综合征中的作用,我们的发现可能潜在地导致识别用于疾病监测的新临床生物标志物和治疗靶点,为治疗这种疾病提供更有效的选择。因此,我们的研究可能为未来的临床干预和靶向免疫治疗提供有价值的证据。