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ProteoGenix
Recombinant Proteins
Mammalian cells
Elisa, WB
Interleukin-27 (IL-27) is a cytokine that plays a crucial role in regulating the immune response. It is composed of two subunits, EBI3 and IL12A, which are both members of the IL-6/IL-12 family of cytokines. IL-27 is produced by various cell types, including dendritic cells, macrophages, and B cells, and has been shown to have both pro- and anti-inflammatory effects. In this article, we will explore the structure, activity, and potential applications of the IL-27 subunits EBI3 and IL12A as drug targets.
EBI3 and IL12A are both glycoproteins that are composed of two subunits, a heavy chain and a light chain, linked by disulfide bonds. EBI3 has a molecular weight of approximately 34 kDa, while IL12A has a molecular weight of around 35 kDa. Both subunits have a similar structure, consisting of four alpha helices and a beta-sheet, and share a common receptor, IL-27 receptor (IL-27R).
EBI3 and IL12A have distinct roles in the immune response, but they also work together to form the heterodimeric cytokine IL-27. EBI3 is known to have anti-inflammatory properties, while IL12A has pro-inflammatory effects. When EBI3 and IL12A bind together, they form the active IL-27 cytokine, which has both pro- and anti-inflammatory effects.
IL-27 has been shown to play a role in promoting T helper 1 (Th1) cell differentiation and inhibiting the development of Th2 cells. This is due to its ability to induce the production of interferon-gamma (IFN-γ) and suppress the production of interleukin-4 (IL-4). IL-27 also has anti-tumor effects, as it can inhibit the growth and survival of certain cancer cells.
The unique structure and activity of EBI3 and IL12A make them potential targets for drug development. Several studies have shown that targeting IL-27 or its subunits can have beneficial effects in various diseases.
As mentioned earlier, EBI3 and IL12A have both pro- and anti-inflammatory effects. This makes them potential targets for the treatment of inflammatory diseases such as rheumatoid arthritis, inflammatory bowel disease, and psoriasis. In a study on a mouse model of rheumatoid arthritis, blocking IL-27 was found to reduce the severity of the disease, suggesting that targeting IL-27 or its subunits could be a promising therapeutic approach.
IL-27 has been shown to have anti-tumor effects, and targeting EBI3 and IL12A could potentially be used in cancer treatment. In a study on melanoma, blocking IL-27 was found to inhibit tumor growth and enhance the anti-tumor immune response. Additionally, IL-27 has been shown to enhance the activity of certain chemotherapeutic drugs, making it a potential adjuvant therapy in cancer treatment.
EBI3 and IL12A have also been studied as potential targets for the treatment of infectious diseases. In a study on tuberculosis, blocking IL-27 was found to reduce the severity of the disease and improve the survival rate in mice. This suggests that targeting IL-27 or its subunits could be a promising approach in treating tuberculosis and other infectious diseases.
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