Combined FXIII-C3 autoantibodies elicit bleeding and complement dysfunction in autoimmune FXIII deficiency

Autoimmune factor XIII (FXIII) deficiency is a rare hemorrhagic disease characterized by severe bleeding and a high mortality rate. However, the pathogenesis of this disease remains unclear. FXIII consumption caused by infections is becoming increasingly common. Our clinical investigation, combined with in vivo experiments, revealed that patients and mice with autoimmune FXIII deficiency displayed complement dysfunction and that pathogenic infection and autoantibody generation were positively correlated. Further analysis revealed the presence of combined FXIII-C3 autoantibodies in patients with autoimmune FXIII deficiency. These combined autoantibodies neutralize FXIII, cause bleeding, and form a complex with C3, inhibiting complement activation and complement-mediated adaptive immune responses. Therefore, compromised immune responses increase host susceptibility to pathogenic Candida albicans infections. Consequently, uncontrolled exogenous fungal infections further activate platelets and cause platelet-related CD40 ligand (CD40L) release. By interacting with the CD40 on the B cell surface, the released CD40L further promotes autoreactive B cell activation to produce more autoantibodies, thereby forming a self-amplification loop for the progressive consumption of FXIII. We believe this study provides a perspective on disease pathogenesis and therapeutic guidance for better treatment of autoimmune FXIII deficiency.

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Publication Details

Journal
Journal of Clinical Investigation
Published
2025-12-09
DOI
https://doi.org/10.1172/jci192619
Primary Topic
Blood properties and coagulation
Type
article
Field-Weighted Citation Impact
0.00

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article

Combined FXIII-C3 autoantibodies elicit bleeding and complement dysfunction in autoimmune FXIII deficiency

Xiang Cheng, Desheng Hu, Yunlun Li, Huafang Wang et al.
Journal of Clinical Investigation
Blood properties and coagulation
article

Combined FXIII-C3 autoantibodies elicit bleeding and complement dysfunction in autoimmune FXIII deficiency

Xiang Cheng, Desheng Hu, Yunlun Li, Huafang Wang, Yaohua Cai, Yu Hu, Liang Tang, Zhipeng Cheng, Heng Mei, Wanting Wang, Lv Xiong, Peter F. Zipfel, Jun Fang, Yuehua Jiang, Bahgat Fayed, Yue Liu, Min Zhang, Lu Zhang, Chaofan Wang, Rui Zhu, Kun Huang, Shanshan Luo, Gensheng Zhang, Chunyan Sun, Yadan Wang, Jun Deng, Yajie Ding
article en

Abstract

Autoimmune factor XIII (FXIII) deficiency is a rare hemorrhagic disease characterized by severe bleeding and a high mortality rate. However, the pathogenesis of this disease remains unclear. FXIII consumption caused by infections is becoming increasingly common. Our clinical investigation, combined with in vivo experiments, revealed that patients and mice with autoimmune FXIII deficiency displayed complement dysfunction and that pathogenic infection and autoantibody generation were positively correlated. Further analysis revealed the presence of combined FXIII-C3 autoantibodies in patients with autoimmune FXIII deficiency. These combined autoantibodies neutralize FXIII, cause bleeding, and form a complex with C3, inhibiting complement activation and complement-mediated adaptive immune responses. Therefore, compromised immune responses increase host susceptibility to pathogenic Candida albicans infections. Consequently, uncontrolled exogenous fungal infections further activate platelets and cause platelet-related CD40 ligand (CD40L) release. By interacting with the CD40 on the B cell surface, the released CD40L further promotes autoreactive B cell activation to produce more autoantibodies, thereby forming a self-amplification loop for the progressive consumption of FXIII. We believe this study provides a perspective on disease pathogenesis and therapeutic guidance for better treatment of autoimmune FXIII deficiency.

Journal of Clinical InvestigationVol. 136(3)
Union Hospital (HK), Shandong University of Traditional Chinese Medicine (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Xiyuan Hospital (CN), National Research Centre (EG), Union Hospital (US), Second Affiliated Hospital of Zhejiang University (CN), Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI) (DE), Union Hospital (CN), Huazhong University of Science and Technology (CN), Friedrich Schiller University Jena (DE)
Huazhong University of Science and Technology, Tongji University, National Science and Technology Major Project, Tongji Medical College, Huazhong University of Science and Technology
Openalex Percentile: Top 42%
Blood properties and coagulation
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