# Cryofibrinogen-associated glomerulonephritis with paraproteinemia

**Authors:** Xuanli Tang, Mengya Jiang, Huaqin Zhang, Peng Bi, Jun Wang, Tian Ye, Jie Zheng, Mengli Tong, Xingyu Zhu, Xiaotao Hou, Shuhua Bao, Yi Lin, Xue Jiang, Hongyu Chen, Feng Wan, Haichun Yang

PMC · DOI: 10.3389/fimmu.2025.1576917 · 2025-07-15

## TL;DR

This paper reports a rare kidney disease case linked to cryofibrinogen and monoclonal immunoglobulin, offering insights into its causes and effects.

## Contribution

The study identifies a cryofibrinogen-MIg complex as a potential cause of glomerular damage in this rare disease.

## Key findings

- Cryofibrinogen and monoclonal immunoglobulin form a complex that may cause kidney damage.
- Cryoprecipitates induced mesangial cell changes and glomerulonephritis in mice.
- The patient partially responded to treatment but relapsed with paraproteinemia.

## Abstract

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.

## Linked entities

- **Proteins:** FGB (fibrinogen beta chain)
- **Diseases:** glomerulonephritis (MONDO:0002462), nephrotic syndrome (MONDO:0005377), chronic kidney failure (MONDO:0024327)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Cxcl9 (C-X-C motif chemokine ligand 9) [NCBI Gene 17329] {aka CMK, Mig, MuMIG, Scyb9, crg-10}, Ighm (immunoglobulin heavy constant mu) [NCBI Gene 16019] {aka Igh-6, Igh-M, Igh6, Igm, TC1460681, muH}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, FGG (fibrinogen gamma chain) [NCBI Gene 2266], Igh-V7183 (immunoglobulin heavy chain (V7183 family)) [NCBI Gene 16059] {aka B9-scFv, IgG, IgH, IgVH1(VSG), VH7183, VI24H}, CXCL9 (C-X-C motif chemokine ligand 9) [NCBI Gene 4283] {aka CMK, Humig, MIG, SCYB9, crg-10}, Fga (fibrinogen alpha chain) [NCBI Gene 14161] {aka Fib}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, LOC105243590 (Ig heavy chain Mem5-like) [NCBI Gene 105243590] {aka IgH, Igg1}, CD68 (CD68 molecule) [NCBI Gene 968] {aka GP110, LAMP4, SCARD1}, Cd68 (CD68 antigen) [NCBI Gene 12514] {aka Lamp4, Scard1, gp110}, FGA (fibrinogen alpha chain) [NCBI Gene 2243] {aka AMYLD2, Fib2}, FN1 (fibronectin 1) [NCBI Gene 2335] {aka CIG, ED-B, FINC, FN, FNZ, GFND}, C3 (complement C3) [NCBI Gene 718] {aka AHUS5, ARMD9, ASP, C3a, C3b, CPAMD1}, Alb (albumin) [NCBI Gene 11657] {aka Alb-1, Alb1, BCL001, BCL002, BPL001}, Igha (immunoglobulin heavy constant alpha) [NCBI Gene 238447] {aka IgA, Igh-2}
- **Diseases:** Myocardial necrosis (MESH:D009336), proteinuria (MESH:D011507), MPGN (MESH:D015432), renal involvement (MESH:C565423), hypertension (MESH:D006973), rash (MESH:D005076), hypertrophy (MESH:D006984), GBM (MESH:D005910), dermatological impairment (MESH:D000168), Cryofibrinogen-associated (MESH:D018886), hematuria (MESH:D006417), vasculitis (MESH:D014657), MGRS (MESH:D008998), abdominal tenderness (MESH:D000007), hyaline thrombi (MESH:D006819), cell (MESH:D002292), mesangial cell injury (MESH:C537346), CF (MESH:C536218), nodular sclerosis (MESH:D008224), autoimmune disease (MESH:D001327), cervical dislocation (MESH:D002575), TMA (MESH:D057049), mitochondrial depletion (MESH:C536350), toxicity (MESH:D064420), chronic kidney disease (MESH:D051436), ICGN (MESH:D007105), lysosomal degeneration (MESH:D016464), infection (MESH:D007239), EM (MESH:D028361), joint swelling (MESH:D007592), multi-organ injury (MESH:D009102), chronic kidney failure (MESH:D007676), carcinoma (MESH:D009369), C3 glomerulonephritis (MESH:C567033), CF-GN (MESH:D005921), glomerular nephritis (MESH:D009393), monoclonal gammopathy of (MESH:D010265), thrombosis (MESH:D013927), cryoglobulinemia (MESH:D003449), Nephrotic syndrome (MESH:D009404), systemic disease (MESH:D034721), proliferative (MESH:D009220), tissue injury (MESH:D017695), edema (MESH:D004487), abnormal renal function (MESH:D007674), IgA nephropathy (MESH:D005922), organ damage (MESH:D000092124), amyloidosis (MESH:D000686), fibronectin glomerulopathy (MESH:C536826), cerebral infarction (MESH:D002544), NS (MESH:D056770)
- **Chemicals:** fluorescein (MESH:D019793), paraffin (MESH:D010232), prednisone (MESH:D011241), sc (MESH:D012538), agarose (MESH:D012685), Pred (MESH:C036266), glutaraldehyde (MESH:D005976), EdU (MESH:C022811), FK506 (MESH:D016559), CTX (MESH:D003520), creatinine (MESH:D003404), atorvastatin (MESH:D000069059), aspirin (MESH:D001241), irbesartan (MESH:D000077405), gold (MESH:D006046), Zoletil (MESH:C006131), Alexa Fluor (AF) 594 (-), EDTA (MESH:D004492), nifedipine (MESH:D009543), AF647 (MESH:C569686)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** c.719-27G>C

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12305703/full.md

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Source: https://tomesphere.com/paper/PMC12305703