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免疫细胞与干燥综合征之间的因果关系:一项单变量、多变量、双向孟德尔随机化研究。

The causal relationship between immune cells and Sjögren's syndrome: a univariate, multivariate, bidirectional Mendelian randomized study.

作者信息

Zeng Wen, Huang Mu, Zeng Yuanyuan, Pan Jie, Qin Fang, Liao Xiaoling, Zheng Leting, Lei Ling

机构信息

Department of Rheumatology and Immunology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.

出版信息

Front Med (Lausanne). 2024 Jul 2;11:1408562. doi: 10.3389/fmed.2024.1408562. eCollection 2024.

DOI:10.3389/fmed.2024.1408562
PMID:39015792
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11249722/
Abstract

INTRODUCTION

Immune cells are involved in the onset and progression of Sjögren's syndrome (SS). This study explored the causal relationship between immune signature cells and SS, which has not been fully elucidated.

METHODS

We conducted univariate, multivariate, and bidirectional Mendelian randomization to investigate the causal relationship between 731 immunological feature characteristic cells and SS pairs and explore the interaction of immune cells in SS.

RESULTS

After false discovery rate correction, six immune cells were significantly associated with SS risk. Among them, four contributed to SS (CD24 on memory B cell, CD27 on IgD + CD24 + B cell, CD28 on CD39+ secreting CD4 Treg cell, and CD80 on CD62L + mDC); two appeared to reduce SS risk (CD3 on CD39 + CD8 + T cell and CD38 on IgD + CD38 + B cell). Pleiotropy and heterogeneity were not observed. Three immune cells exerted independent effects for SS (CD27 on IgD + CD24 + B cell, CD80 on CD62L + mDC, and CD38 on IgD + CD38 + B cell); two were risk factors (CD27 on IgD + CD24 + B cell and CD80 on CD62L + mDC); and one was a protective factor (CD38 on IgD + CD38 + B cell). Twenty-three immune cells showed a reverse causal relationship with SS.

CONCLUSION

These findings demonstrate the influence of immune cells on SS risk and the effects of SS on immune cells, providing new clues for further research on the mechanisms underlying SS.

摘要

引言

免疫细胞参与干燥综合征(SS)的发病和进展。本研究探讨了免疫特征细胞与SS之间尚未完全阐明的因果关系。

方法

我们进行了单变量、多变量和双向孟德尔随机化,以研究731个免疫特征性细胞与SS之间的因果关系,并探讨SS中免疫细胞的相互作用。

结果

经过错误发现率校正后,六种免疫细胞与SS风险显著相关。其中,四种细胞增加SS风险(记忆B细胞上的CD24、IgD+CD24+B细胞上的CD27、CD39+分泌CD4调节性T细胞上的CD28以及CD62L+mDC上的CD80);两种细胞似乎降低SS风险(CD39+CD8+T细胞上的CD3以及IgD+CD38+B细胞上的CD38)。未观察到多效性和异质性。三种免疫细胞对SS有独立影响(IgD+CD24+B细胞上的CD27、CD62L+mDC上的CD80以及IgD+CD38+B细胞上的CD38);两种是危险因素(IgD+CD24+B细胞上的CD27和CD62L+mDC上的CD80);一种是保护因素(IgD+CD38+B细胞上的CD38)。二十三种免疫细胞与SS呈反向因果关系。

结论

这些发现证明了免疫细胞对SS风险的影响以及SS对免疫细胞的作用,为进一步研究SS潜在机制提供了新线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d33/11249722/00130393ec49/fmed-11-1408562-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d33/11249722/eb1f4a416315/fmed-11-1408562-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d33/11249722/8d6407f3dc77/fmed-11-1408562-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d33/11249722/00130393ec49/fmed-11-1408562-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d33/11249722/eb1f4a416315/fmed-11-1408562-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d33/11249722/8d6407f3dc77/fmed-11-1408562-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d33/11249722/00130393ec49/fmed-11-1408562-g003.jpg

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