Interleukin 17A

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Interleukin 17A (IL-17A), also known as IL-17, is a pro-inflammatory cytokine that plays a crucial role in the immune system, particularly in the defense against extracellular pathogens and in the pathogenesis of various autoimmune diseases. It is a member of the IL-17 family, which includes several other cytokines (IL-17B through IL-17F), but IL-17A is the most studied and well-characterized among them.

Structure and Function[edit | edit source]

IL-17A is primarily produced by a subset of T helper cells known as Th17 cells following their activation. It can also be secreted by other immune cells, including gamma delta T cells (γδ T cells), natural killer cells, and innate lymphoid cells. IL-17A functions by binding to its receptor, IL-17R, which is expressed on various cell types, including epithelial cells, fibroblasts, and macrophages. This binding initiates a signaling cascade that leads to the production of other pro-inflammatory cytokines (such as IL-6 and TNF-α), chemokines, and metalloproteases, thereby amplifying the inflammatory response.

Role in Disease[edit | edit source]

While IL-17A is vital for defending against certain pathogens, its dysregulation is implicated in the pathogenesis of several autoimmune and inflammatory diseases, such as psoriasis, rheumatoid arthritis, and multiple sclerosis. In these conditions, the overproduction of IL-17A contributes to tissue inflammation and damage. Consequently, targeting IL-17A through the use of monoclonal antibodies has emerged as a therapeutic strategy for managing these diseases.

Therapeutic Target[edit | edit source]

Several biologic drugs that inhibit IL-17A have been developed and approved for clinical use. These include secukinumab and ixekizumab, which are used to treat conditions like psoriasis, psoriatic arthritis, and ankylosing spondylitis. By neutralizing IL-17A, these drugs help reduce inflammation, alleviate symptoms, and prevent disease progression.

Research Directions[edit | edit source]

Research on IL-17A continues to uncover its roles in various physiological and pathological processes. Studies are exploring its involvement in other diseases, such as inflammatory bowel disease and certain types of cancer, to understand whether targeting IL-17A could be beneficial. Additionally, the mechanisms regulating IL-17A production and its interactions with other components of the immune system are subjects of ongoing investigation.

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Contributors: Prab R. Tumpati, MD