Target intelligence / Profile preview

Interleukin-27 subunit beta (EBI3)

Target
EBI3
Molecular classification
Cytokine subunit, Secreted glycoprotein, Interleukin family, Hematopoietin receptor family member
01

Overview

Interleukin-27 subunit beta (EBI3) is a secreted glycoprotein identified by its induction in B lymphocytes following Epstein-Barr virus infection[5][7]. It is homologous to the p40 subunit of interleukin-12 and is a structural component of two key heterodimeric cytokines: IL-27 (where it combines with p28) and IL-35 (where it combines with IL-12p35)[5][7][8]. EBI3 participates in immune regulation by modulating T cell differentiation (TH1, TH2, TH17), promoting or inhibiting inflammation, and contributing to anti-tumor and antiangiogenic activities[1][5][7]. Besides its extracellular cytokine functions, EBI3 can act intracellularly as a chaperone, aiding in protein folding, notably enhancing expression of the IL-23 receptor alpha chain in T cells[3]. EBI3 is involved in immune responses, inflammation, infection, cancer progression, and autoimmune processes, but is not directly targeted by clinical drugs as of current knowledge.

Other names
IL-27 subunit betaIL27BIL-27BEpstein-Barr virus induced gene 3 proteinEBV-induced gene 3Epstein-Barr virus-induced gene 3 proteinIL35BIL-35BEBV-induced gene 3 proteininterleukin-27 subunit betaIL-27bIL-35 subunitEBI3
02

Mechanism of action

Modulates immune signaling as part of IL-27 and IL-35 heterodimeric cytokines, activating or suppressing various immune cell functions including TH1, TH2, and regulatory T cell responses[5][7][8].

03

Biological functions

Immune response regulationCytokine signalingT-helper cell developmentModulation of inflammationPromotion of protein folding (intracellular function with IL-23Rα)
04

Disease associations

InfectionCancerInflammationAutoimmune disease
05

Safety considerations

Reduction or dysregulation may contribute to immune dysfunction or pathological inflammation[1][3].Modulation could risk unwanted immunosuppression or heightened inflammation depending on context.
06

Interacting drugs

None directly reported (as of available sources). However, molecules modulating IL-27 or IL-35 pathways, such as experimental antibodies, may indirectly target this protein.
07

Biomarkers

Elevated as a potential biomarker in certain infections, cancers, or inflammatory diseases. Exact validated use as a clinical biomarker is not established from current sources.

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