The IL17F gene is located on chromosome 6p12 and was discovered in 2001. This cytokine can be secreted as disulfide-linked homodimer or heterodimer.[9][10]
IL-17F is highly (55%) homologous to interleukin-17A (IL-17A). These two molecules bind to the same receptors and are very likely to have similar biological functions. IL-17A and IL-17F are often co-expressed. However, IL-17F is a weaker inducer of pro-inflammatory cytokine expression and is produced by a wider range of cell types than IL-17A. Another difference lies in the binding affinities for their receptors: IL-17A binds more strongly to IL-17RA, IL-17F to IL-17RC.[7][12][13]
The interleukin 17 family members are among the effector cytokines of Th17 immune response. This immune response protects hosts from pathogens at epithelial and mucosal tissues including the skin, lung, and intestine. The Th17-type immune response is directed primarily against extracellular bacteria. IL-17F as an effector cytokine of Th17 cells is involved in host defense against bacterial infections. It has many mechanisms by which it helps resist bacteria. IL-17F has the ability to stimulate the production of defensins and other antimicrobial peptides; it can also resist bacteria through production of pro-inflammatory cytokines and chemokines that attract neutrophils and other effector cells.[7][14]
Clinical significance
IL-17F is a proinflammatory cytokine associated with many diseases. It very often plays crucial role in autoimmune diseases.
One of the diseases associated with IL-17F is psoriasis. Levels of IL-17F, as well as the levels of IL-17A, are increased in psoriatic skin and in synovial cells in psoriatic arthritis. IL-17F is capable of inducing cartilage matrix release and can inhibit the synthesis of new cartilage matrix. The monoclonal antibodybimekizumab against IL-17A and IL-17F is approved in Europe for the treatment of psoriasis; it may also be useful in the treatment of ankylosing spondylitis.[15][16]
IL-17F plays an important role in asthma and allergic airway inflammation. IL-17F has been well characterized both in vitro and in vivo to have a pro-inflammatory role in asthma. IL-17F was originally found in bronchoalveolar lavage cells from patients with allergic asthma upon ragweed allergen stimulation. The expression level of IL-17F correlates with the severity of the disease. Overexpression of this cytokine in the airway is associated with neutrophilia, secretion of many cytokines, increased airway activity and mucus hypersecretion.[9]
Increased expression of IL-17F is also found in neuronal inflammation—specifically, in active lesion sites in experimental autoimmune encephalitis, an animal model of multiple sclerosis. IL-17F together with IL-17A contributes to chronic inflammation.[16]
IL-17F may also be involved in tumorigenesis and associated with the tumor microenvironment (TME), as pro-tumor and anti-tumor functions have been ascribed to the related protein IL-17A has. However, a role for IL-17F in tumor development has not been well described.[7]
^"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^Linares-Pineda TM, Cañadas-Garre M, Sánchez-Pozo A, Calleja-Hernández MÁ (November 2016). "Gene polymorphisms as predictors of response to biological therapies in psoriasis patients". Pharmacological Research. 113 (Pt A): 71–80. doi:10.1016/j.phrs.2016.07.020. PMID27524442.
^Moseley TA, Haudenschild DR, Rose L, Reddi AH (April 2003). "Interleukin-17 family and IL-17 receptors". Cytokine & Growth Factor Reviews. 14 (2): 155–174. doi:10.1016/S1359-6101(03)00002-9. PMID12651226.
^ abcKawaguchi M, Kokubu F, Fujita J, Huang SK, Hizawa N (December 2009). "Role of interleukin-17F in asthma". Inflammation & Allergy - Drug Targets. 8 (5): 383–389. doi:10.2174/1871528110908050383. PMID20025586.
^Gorczynski RM (2020). "IL-17 Signaling in the Tumor Microenvironment". In Birbrair A (ed.). Tumor Microenvironment. Advances in Experimental Medicine and Biology. Vol. 1240. Cham: Springer International Publishing. pp. 47–58. doi:10.1007/978-3-030-38315-2_4. ISBN978-3-030-38314-5. PMID32060887. S2CID211122697.
^Reis J, Vender R, Torres T (August 2019). "Bimekizumab: The First Dual Inhibitor of Interleukin (IL)-17A and IL-17F for the Treatment of Psoriatic Disease and Ankylosing Spondylitis". BioDrugs. 33 (4): 391–399. doi:10.1007/s40259-019-00361-6. PMID31172372. S2CID174812750.