IL12 is a cytokine secreted by phagocytes and dendritic cells and that induces interferon-gamma production by natural-killer and T lymphocytes. It consists of two subunits encoded by IL12A and IL12B. The clinical syndrome is rare and its inheritance may differ between kindreds. Although autosomal recessive in most cases, autosomal dominant and X-linked recessive inheritance have been reported. These disorders generally manifest in childhood, although they may become apparent during adulthood.
Alternative names
IL12 p40 deficiency
Classification
- Defects of innate immune system, receptors and signaling components
Inheritance
Autosomal recessive
Cross references
Phenotypically related immunodeficiencies
IDR factfile for IFNγ1-receptor deficiency
IDR factfile for IFNγ2-receptor deficiency
Incidence
Incidence is not known.