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Autoimmune disease-associated lymphomas: research progress and review
Chengqian Chen1, Wei Guo1, Yangzhi Zhao1
1Department of Hematology, The First Hospital of Jilin University, Changchun, China.
Autoimmune diseases significantly increase lymphoma risk, especially diffuse large B-cell lymphoma and MALT lymphoma. Chronic inflammation, immune dysfunction, and autoantibodies drive oncogenesis, requiring careful management balancing inflammation control and treatment risks.
Area of Science:
- Immunology
- Oncology
- Epidemiology
Background:
- Autoimmune diseases (ADs) are linked to a higher risk of lymphoma.
- Sjögren's disease shows a particularly high standardized incidence ratio (SIR) for lymphoma.
- Diffuse large B-cell lymphoma (DLBCL) and mucosa-associated lymphoid tissue (MALT) lymphoma are common subtypes in ADs.
Purpose of the Study:
- To systematically review the epidemiology, pathogenesis, risk factors, and treatment of lymphomas associated with autoimmune diseases.
- To elucidate the bidirectional relationship between ADs and specific lymphoma subtypes.
- To explore the role of immune dysregulation and external factors in ADs-associated lymphomagenesis.
Main Methods:
- Systematic review of epidemiological studies.
- Analysis of pathological mechanisms including immune-inflammatory pathways.
- Evaluation of risk factors, including intrinsic disease features, treatments, and gene-environment interactions.
- Review of current and emerging therapeutic strategies.
Main Results:
- Strong epidemiological links exist between ADs (e.g., rheumatoid arthritis, systemic lupus erythematosus, Sjögren's disease) and lymphoma subtypes.
- Chronic inflammation, regulatory cell dysfunction, and autoantibodies are key pathogenic drivers.
- Epstein-Barr virus and immune complexes contribute to oncogenesis.
- Risk factors are multifactorial, involving disease characteristics, treatments, and environmental exposures.
Conclusions:
- Managing ADs-associated lymphomas requires balancing inflammation control with minimizing treatment risks.
- Targeted therapies (rituximab, BTK inhibitors) and HSCT show promise but are influenced by immune status.
- Future research should focus on multi-omics for risk stratification, novel immunotherapies, and optimized care models.
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