Eosinophil-derived neurotoxin

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Eosinophil-derived neurotoxin (EDN), also known as RNase 2, is a protein with antiviral properties that is produced by eosinophils, a type of white blood cell. Part of the ribonuclease A superfamily, EDN is closely related to the eosinophil cationic protein (ECP) and shares a significant sequence homology with it. Eosinophils are known for their role in the body's immune response, particularly in combating parasitic infections and in the development of allergic reactions. EDN contributes to the immune defense by degrading viral RNA, thereby inhibiting viral replication.

Function[edit | edit source]

EDN exerts its antiviral effects through the degradation of viral RNA, which is crucial for the replication of viruses. This activity is not limited to any specific type of virus, making EDN a broad-spectrum antiviral agent. In addition to its antiviral properties, EDN has been implicated in modulating the immune system's response during allergic reactions and asthma. It does so by inducing chemotaxis of dendritic cells and influencing T-cell responses, which are essential components of the adaptive immune system.

Clinical Significance[edit | edit source]

The role of EDN in disease has been a subject of research, particularly in the context of allergic diseases such as asthma, rhinitis, and atopic dermatitis. Elevated levels of EDN have been observed in patients suffering from these conditions, suggesting its involvement in the pathogenesis of allergic reactions. Furthermore, EDN levels in bodily fluids are considered potential biomarkers for the diagnosis and monitoring of disease activity in eosinophil-associated disorders.

Genetics[edit | edit source]

The gene encoding eosinophil-derived neurotoxin is located on chromosome 14, along with other genes that encode for the eosinophil ribonucleases. Genetic variations in this region have been studied for their association with susceptibility to allergic diseases and asthma.

Therapeutic Potential[edit | edit source]

Given its antiviral and immunomodulatory properties, there is interest in exploring EDN as a therapeutic agent. Its ability to degrade viral RNA suggests potential applications in the treatment of viral infections. Additionally, modulating EDN activity could offer new approaches to managing allergic diseases by influencing eosinophil function and the immune response.

See Also[edit | edit source]

References[edit | edit source]



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Contributors: Prab R. Tumpati, MD