Tang Xuanli, Jiang Mengya, Zhang Huaqin, Bi Peng, Wang Jun, Ye Tian, Zheng Jie, Tong Mengli, Zhu Xingyu, Hou Xiaotao, Bao Shuhua, Lin Yi, Jiang Xue, Chen Hongyu, Wan Feng, Yang Haichun
Department of Nephrology, Hangzhou TCM Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, China.
Department of Renal Pathology, King Medical Diagnostics Center, Guangzhou, China.
Front Immunol. 2025 Jul 15;16:1576917. doi: 10.3389/fimmu.2025.1576917. eCollection 2025.
Cryofibrinogen-associated glomerulonephritis (CF-GN) is a rare disease that lacks comprehensive research and requires further investigation to improve our understanding of its pathophysiology.
Based on the morphological findings from a kidney biopsy and blood tests, an elderly patient was diagnosed with CF-GN. Biological materials obtained from peripheral blood were utilized to treat cultured mesangial cells and mice.
The patient presented with nephrotic syndrome and chronic kidney failure. The biopsy revealed a membranoproliferative glomerulonephritis pattern with distinct substructures and positive fibrinogen staining. Cryofibrinogen was detectable under cold conditions, and monoclonal immunoglobulin (MIg) was exclusively identified within cryoprecipitates. Genetic analysis uncovered an intronic mutation. The patient partially responded to immunosuppressive therapy, but later relapsed with paraproteinemia, and the MIg was detected to have cryoactivity. To investigate the pathophysiology of CF-GN further, its cryoactivity was detected when mixing the serum (with or without MIg) with healthy control plasma. When exposed to the patient's cryoprecipitates, cultured mesangial cells showed significant proliferation, phagocytosis of fibrinogen, and lysosomal degeneration. Injection of these cryoprecipitates into mice induced proliferative glomerulonephritis and other organ damage.
This study provides valuable insights into the diagnosis, treatment, and pathophysiology of CF-GN with paraproteinemia. The identification of the complex of cryofibrinogen and MIg as a potential mechanism of glomerular damage shed light on the pathogenesis of this rare disease.
冷纤维蛋白原相关肾小球肾炎(CF - GN)是一种罕见疾病,目前缺乏全面研究,需要进一步调查以增进我们对其病理生理学的理解。
根据肾活检的形态学结果和血液检测,一名老年患者被诊断为CF - GN。利用从外周血获取的生物材料处理培养的系膜细胞和小鼠。
该患者表现为肾病综合征和慢性肾衰竭。活检显示为膜增生性肾小球肾炎模式,具有明显的亚结构且纤维蛋白原染色呈阳性。在寒冷条件下可检测到冷纤维蛋白原,且单克隆免疫球蛋白(MIg)仅在冷沉淀物中被鉴定出来。基因分析发现一个内含子突变。患者对免疫抑制治疗部分有反应,但后来因副蛋白血症复发,且检测到MIg具有冷活性。为进一步研究CF - GN的病理生理学,将血清(含或不含MIg)与健康对照血浆混合时检测到其冷活性。当暴露于患者的冷沉淀物时,培养的系膜细胞显示出显著增殖、纤维蛋白原吞噬作用以及溶酶体变性。将这些冷沉淀物注射到小鼠体内可诱导增生性肾小球肾炎和其他器官损伤。
本研究为伴有副蛋白血症的CF - GN的诊断、治疗和病理生理学提供了有价值的见解。冷纤维蛋白原和MIg复合物被确定为肾小球损伤的潜在机制,这为这种罕见疾病的发病机制提供了线索。