# Hypereosinophilic syndrome with elevated IgG4 and T-cell clonality: A report of two cases

**Authors:** Meichun Huang, Limin Wang, Xiuxiu Li, Ying Lu

PMC · DOI: 10.1515/biol-2025-1138 · Open Life Sciences · 2025-07-24

## TL;DR

This paper presents two rare cases of hypereosinophilic syndrome with elevated IgG4 and T-cell clonality, highlighting the need for detailed evaluations to guide treatment.

## Contribution

The study reports two complex and rare cases linking hypereosinophilic syndrome with elevated IgG4 and T-cell clonality.

## Key findings

- The first case showed elevated IgG4, eosinophilia, and T-cell clonality with features resembling EGPA and IgG4-related nephritis.
- The second case also exhibited elevated IgG4 and eosinophilia with T-cell clonality, suggesting a rare overlap of conditions.
- The study emphasizes the importance of pathological and genetic evaluations in such complex cases for better treatment outcomes.

## Abstract

In some cases, higher IgG4 levels are accompanied by increased circulating IgE, higher eosinophil counts, and various autoantibodies. Among these cases, IgG4-related disease (IgG4-RD) is one of the most frequently diagnosed conditions. This study reported two particularly complex and rare cases of hypereosinophilic syndrome (HES) associated with elevated IgG4 and T-cell clonality. The first case involved T-cell clonality complicated by HES and IgG4-RD, presenting with clinical features resembling eosinophilic granulomatosis with polyangiitis (EGPA). Laboratory findings showed a serum IgG4 concentration of 8.74 g/L, an IgG4/IgG ratio of 40.58%, and positive results for P-anti-neutrophil cytoplasmic antibodies (ANCA) and myeloperoxidase-ANCA. Renal biopsy findings were consistent with IgG4-related interstitial nephritis. However, routine hematological testing revealed a markedly elevated eosinophil count of 14.75 × 109/L and eosinophilic infiltration in both lymph nodes and kidney tissue. Furthermore, monoclonal rearrangements of the T-cell receptor gamma and delta genes were identified. The second patient was ultimately diagnosed with HES with elevated IgG4 and T-cell clonality, with an elevated IgG4 concentration of 2.458 g/L and an eosinophil count of 14.75 × 109/L. In conclusion, in cases presenting with elevated IgG4 levels and hypereosinophilia, further pathological and genetic evaluations may be essential to guide appropriate and timely treatment, improving patient prognosis.

## Linked entities

- **Proteins:** IGG (Immunoglobulin G level)
- **Diseases:** hypereosinophilic syndrome (MONDO:0015691), IgG4-related disease (MONDO:0017287), eosinophilic granulomatosis with polyangiitis (MONDO:0015943)

## Full-text entities

- **Genes:** MPO (myeloperoxidase) [NCBI Gene 4353], IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}
- **Diseases:** interstitial nephritis (MESH:D009395), HES (MESH:D017681), hypereosinophilia (MESH:D004802), EGPA (MESH:D014890), anti (MESH:D006679), IgG4 (MESH:D000077733)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12290366