TNF-alpha
Synonym(s)
DefinitionThis section has been translated automatically.
Multifunctional proinflammatory cytokine that is centrally involved in local and systemic inflammation. TNF-alpha is one of the best-studied members of the so-called TNF/TNFR superfamily, a cytokine system that assumes central functions in the immune response and in organogenesis, particularly in the lymphatic system. It plays a central role in the pathogenesis of psoriasis and other inflammatory processes (Crohn's disease, arthritis; pathogenesis of contact allergy). It causes hemorrhagic necrosis in certain tumors.
General informationThis section has been translated automatically.
TNF-alpha exists biologically in soluble or transmembrane-bound form. TNF-alpha molecules interact with at least 2 receptors (tumor necrosis factor receptor superfamily member 1A(TNFRSF1A) or tumor necrosis factor receptor superfamily member 1B (TNFRSF1B).
The interaction of TNF-alpha with its receptors activates signaling cascades that can lead to apoptosis (via caspase-8; see caspases below) and cell activation (via NF-κB) (Note: NF-kappaB/=nuclear factor-kappa B, is a fast-acting primary transcription factor that occurs in all cell types. It is involved in cellular responses to stimuli such as cytokines and stress and plays a key role in regulating the immunological response to infections (see also under transcription factors).
The balance of antagonistic effects of both signaling inductions depends on the cellular environment in which the stimulation by TNF-alpha occurs. The NF-κB-mediated reaction is relevant for inflammation, in the course of which pro-inflammatory enzymes such as interleukins (especially interleukin-6 and interleukin-8) are released.
OccurrenceThis section has been translated automatically.
TNF-alpha is mainly produced and released by macrophages, but also by a large number of other cells such as lymphocytes, mast cells, endothelial cells, cardiac muscle cells, fibroblasts and neuronal tissue. Large amounts of TNF-alpha are released in response to bacterial products (e.g. lipopolysaccharides) and interleukin-1beta (seeinterleukin-1 below). The formation is stimulated via Toll-like receptors and the MAP signaling pathway as well as NF-kappaB. It also has effects on lipid metabolism, blood coagulation, insulin resistance and various endothelial functions.
TherapyThis section has been translated automatically.
TNF-alpha and its interactions with its receptors are pharmacologically important targets of various drug classes. Drug classes that are effective in the biological immunotherapy of various diseases, including Crohn's disease, rheumatoid arthritis and psoriasis. See also infliximab, etanercept, golimumab.
Note(s)This section has been translated automatically.
TNF-alpha was described as early as 1975 as a cytokine that plays a role in bacterial diseases.
LiteratureThis section has been translated automatically.
- Alexis A et al (2005) Off-label dermatologic uses of anti-TNF-a therapies. J Cutan Med Surg 9: 296-302
- Wakefield PE, James WD et al (1991) Tumor necrosis factor. J Am Acad Dermatol 24: 675-685
- Carter PH et al (2001) Photochemically enhanced binding of small molecules to the tumor necrosis factor receptor-1 inhibits the binding of TNF-α. PNAS 98: 11879-11884
- Hehlgans, T et al (2005) The intriguing biology of the tumour necrosis factor/tumour necrosis factor receptor superfamily: players, rules and the games. Immunology 115: 1-20
- Seneschal J et al (2007) Psoriasiform drug eruptions under anti-TNF treatment of arthritis are not true psoriasis. Acta Derm Venereol 87: 77-80
- Tracey KJ (2002) The inflammatory reflex. Nature 420: 853-859