CXCL8

C-X-C motif chemokine ligand 8

Summary

The protein encoded by this gene is a member of the CXC chemokine family and is a major mediator of the inflammatory response. The encoded protein is commonly referred to as interleukin-8 (IL-8). IL-8 is secreted by mononuclear macrophages, neutrophils, eosinophils, T lymphocytes, epithelial cells, and fibroblasts. It functions as a chemotactic factor by guiding the neutrophils to the site of infection. Bacterial and viral products rapidly induce IL-8 expression. IL-8 also participates with other cytokines in the proinflammatory signaling cascade and plays a role in systemic inflammatory response syndrome (SIRS). This gene is believed to play a role in the pathogenesis of the lower respiratory tract infection bronchiolitis, a common respiratory tract disease caused by the respiratory syncytial virus (RSV). The overproduction of this proinflammatory protein is thought to cause the lung inflammation associated with csytic fibrosis. This proinflammatory protein is also suspected of playing a role in coronary artery disease and endothelial dysfunction. This protein is also secreted by tumor cells and promotes tumor migration, invasion, angiogenesis and metastasis. This chemokine is also a potent angiogenic factor. The binding of IL-8 to one of its receptors (IL-8RB/CXCR2) increases the permeability of blood vessels and increasing levels of IL-8 are positively correlated with increased severity of multiple disease outcomes (eg, sepsis). This gene and other members of the CXC chemokine gene family form a gene cluster in a region of chromosome 4q. [provided by RefSeq, May 2020]

Known Variants12 total

rsidPosition (GRCh37)AllelesClassClinVar
rs22275324:74,605,532T/Cupstream gene variant
rs40734:74,606,024A/Tregulatory region variantother
rs18032054:74,606,393C/Tlikely benign
rs1848740174:74,606,444G/Clikely benign
rs22273074:74,606,669T/C
rs22273064:74,607,055C/Tregulatory region variant
rs1883786694:74,607,285G/Tlikely benign
rs14223500434:74,607,340T/Cuncertain significance
rs17291874634:74,607,718G/Auncertain significance
rs22275504:74,608,923T/C3 prime UTR variant
rs11266474:74,609,045A/C
rs131129104:74,609,755A/C

Gene information from NCBI Gene. Variant classifications from ClinVar.