Interleukins (ILs) are a group ofcytokines (secretedproteins andsignal molecules) that are expressed and secreted bywhite blood cells (leukocytes) as well as some other body cells. Thehuman genome encodes more than 50 interleukins and related proteins.[1]
The function of theimmune system primarily depends on interleukins, andrare deficiencies of a number of them have been described, all featuringautoimmune diseases orimmune deficiency. The majority of interleukins are synthesized byCD4 helper T-lymphocytes, as well as throughmonocytes,macrophages, andendothelial cells. They promote the development and differentiation of T andB lymphocytes, andhematopoietic cells.
Interleukin receptors onastrocytes in thehippocampus are also known to be involved in the development of spatial memories in mice.[2]
The name "interleukin" was chosen in 1979, to replace the various different names used by different research groups to designateinterleukin 1 (lymphocyte activating factor, mitogenic protein, T-cell replacing factor III, B-cell activating factor, B-cell differentiation factor, and "Heidikine") andinterleukin 2 (TSF, etc.). This decision was taken during the Second International Lymphokine Workshop inSwitzerland (27–31 May 1979 inErmatingen).[3][4][5]
The terminterleukin derives from (inter-) "as a means of communication", and (-leukin) "deriving from the fact that many of these proteins are produced by leukocytes and act on leukocytes". The name is something of a relic; it has since been found that interleukins are produced by a wide variety of body cells. The term was coined by Dr Vern Paetkau,University of Victoria.
Some interleukins are classified aslymphokines, lymphocyte-produced cytokines that mediate immune responses.
Interleukin 1 alpha and interleukin 1 beta (IL1 alpha andIL1 beta) are cytokines that participate in the regulation of immune responses, inflammatory reactions, and hematopoiesis.[6] Two types of IL-1 receptor, each with three extracellular immunoglobulin (Ig)-like domains, limited sequence similarity (28%) and different pharmacological characteristics have been cloned from mouse and human cell lines: these have been termed type I and type II receptors.[7] The receptors both exist in transmembrane (TM) and soluble forms: the soluble IL-1 receptor is thought to be post-translationally derived from cleavage of the extracellular portion of the membrane receptors.
Both IL-1 receptors (CD121a/IL1R1,CD121b/IL1R2) appear to be well conserved in evolution, and map to the same chromosomal location.[8] The receptors can both bind all three forms of IL-1 (IL-1 alpha, IL-1 beta andIL-1 receptor antagonist).
The crystal structures of IL1A and IL1B[9] have been solved, showing them to share the same 12-stranded beta-sheet structure as both theheparin binding growth factors and the Kunitz-type soybean trypsin inhibitors.[10] The beta-sheets are arranged in 4 similar lobes around a central axis, 8 strands forming an anti-parallel beta-barrel. Several regions, especially the loop between strands 4 and 5, have been implicated in receptor binding.
Molecular cloning of the Interleukin 1 Beta converting enzyme is generated by the proteolytic cleavage of an inactive precursor molecule. A complementary DNA encoding protease that carries out this cleavage has been cloned. Recombinant expression enables cells to process precursor Interleukin 1 Beta to the mature form of the enzyme.
Interleukin 1 also plays a role in thecentral nervous system. Research indicates that mice with a genetic deletion of the type I IL-1 receptor display markedly impaired hippocampal-dependent memory functioning andlong-term potentiation, although memories that do not depend on the integrity of thehippocampus seem to be spared.[2][11] However, when mice with this genetic deletion have wild-typeneural precursor cells injected into theirhippocampus and these cells are allowed to mature intoastrocytes containing the interleukin-1 receptors, the mice exhibit normal hippocampal-dependent memory function, and partial restoration oflong-term potentiation.[2]
T lymphocytes regulate the growth and differentiation of T cells and certain B cells through the release of secreted protein factors.[12] These factors, which includeinterleukin 2 (IL2), are secreted by lectin- or antigen-stimulated T cells, and have various physiological effects. IL2 is a lymphokine that induces the proliferation of responsive T cells. In addition, it acts on some B cells, via receptor-specific binding,[13] as a growth factor and antibody production stimulant.[14] The protein is secreted as a single glycosylated polypeptide, and cleavage of a signal sequence is required for its activity.[13] Solution NMR suggests that the structure of IL2 comprises a bundle of 4 helices (termed A-D), flanked by 2 shorter helices and several poorly defined loops. Residues in helix A, and in the loop region between helices A and B, are important for receptor binding. Secondary structure analysis has suggested similarity to IL4 and granulocyte-macrophage colony stimulating factor (GMCSF).[14]
Interleukin 3 (IL3) is a cytokine that regulateshematopoiesis by controlling the production, differentiation and function of granulocytes and macrophages.[15][16] The protein, which exists in vivo as a monomer, is produced in activated T cells and mast cells,[15][16] and is activated by the cleavage of an N-terminal signal sequence.[16]
IL3 is produced by T lymphocytes and T-cell lymphomas only after stimulation with antigens, mitogens, or chemical activators such as phorbol esters. However, IL3 is constitutively expressed in the myelomonocytic leukaemia cell line WEHI-3B.[16] It is thought that the genetic change of the cell line to constitutive production of IL3 is the key event in development of this leukaemia.[16]
Interleukin 4 (IL4) is produced by CD4+ T cells specialized in providing help to B cells to proliferate and to undergo class switch recombination and somatic hypermutation. Th2 cells, through production of IL-4, have an important function in B-cell responses that involve class switch recombination to the IgG1 and IgE isotypes.
Interleukin 5 (IL5), also known aseosinophil differentiation factor (EDF), is a lineage-specific cytokine for eosinophilpoiesis.[17][18] It regulates eosinophil growth and activation,[17] and thus plays an important role in diseases associated with increased levels of eosinophils, including asthma.[18] IL5 has a similar overall fold to other cytokines (e.g., IL2, IL4 and GCSF),[18] but while these exist as monomeric structures, IL5 is a homodimer. The fold contains an anti-parallel 4-alpha-helix bundle with a left handed twist, connected by a 2-stranded anti-parallel beta-sheet.[18][19] The monomers are held together by 2 interchain disulphide bonds.[19]
Interleukin 6 (IL6), also referred to as B-cell stimulatory factor-2 (BSF-2) and interferon beta-2, is a cytokine involved in a wide variety of biological functions.[20] It plays an essential role in the final differentiation of B cells into immunoglobulin-secreting cells, as well as inducing myeloma/plasmacytoma growth, nerve cell differentiation, and, in hepatocytes, acute-phase reactants.[20][21]
A number of other cytokines may be grouped with IL6 on the basis of sequence similarity.[20][21][22] These include granulocyte colony-stimulating factor (GCSF) and myelomonocytic growth factor (MGF). GCSF acts in hematopoiesis by affecting the production, differentiation, and function of two related white cell groups in the blood.[22] MGF also acts in hematopoiesis, stimulating proliferation and colony formation of normal and transformed avian cells of the myeloid lineage.
Cytokines of the IL6/GCSF/MGF family are glycoproteins of about 170 to 180 amino acid residues that contain four conserved cysteine residues involved in two disulphide bonds.[22] They have a compact, globular fold (similar to other interleukins), stabilised by the two disulphide bonds. One half of the structure is dominated by a 4-alpha-helix bundle with a left-handed twist;[23] the helices are anti-parallel, with two overhand connections, which fall into a double-stranded anti-parallel beta-sheet. The fourth alpha-helix is important to thebiological activity of the molecule.[21]
Interleukin 7 (IL-7)[24] is a cytokine that serves as a growth factor for early lymphoid cells of both B- and T-cell lineages.
Interleukin 8 is achemokine produced bymacrophages and other cell types such asepithelial cells, airway smooth muscle cells[25] and endothelial cells.Endothelial cells store IL-8 in their storage vesicles, theWeibel-Palade bodies.[26][27] In humans, the interleukin-8protein is encoded by theCXCL8gene.[28] IL-8 is initially produced as a precursor peptide of 99 amino acids which then undergoes cleavage to create several active IL-8 isoforms.[29] In culture, a 72 amino acid peptide is the major form secreted by macrophages.[29]
There are many receptors on the surface membrane capable of binding IL-8; the most frequently studied types are theG protein-coupled serpentine receptorsCXCR1 andCXCR2. Expression and affinity for IL-8 differs between the two receptors (CXCR1 > CXCR2). Through a chain of biochemical reactions, IL-8 is secreted and is an important mediator of the immune reaction in the innate immune system response.
Interleukin 9 (IL-9)[30] is a cytokine that supports IL-2 independent and IL-4 independent growth of helper T cells. Early studies had indicated that Interleukin 9 and 7 seem to be evolutionary related[31] and Pfam, InterPro and PROSITE entries exist for interleukin 7/interleukin 9 family. However, a recent study[32] has shown that IL-9 is, in fact, much closer to both IL-2 and IL-15, than to IL-7. Moreover, the study showed irreconcilable structural differences between IL-7 and all the remaining cytokines signalling through theγc receptor ( IL-2, IL-4, IL-7, IL-9, IL-15 and IL-21).
Interleukin 10 (IL-10) is a protein that inhibits the synthesis of a number of cytokines, including IFN-gamma, IL-2, IL-3, TNF, and GM-CSF produced by activated macrophages and by helper T cells. In structure, IL-10 is a protein of about 160 amino acids that contains four conserved cysteines involved in disulphide bonds.[33] IL-10 is highly similar to theHuman herpesvirus 4 (Epstein-Barr virus) BCRF1 protein, which inhibits the synthesis of gamma-interferon and toEquid herpesvirus 2 (Equine herpesvirus 2) protein E7. It is also similar, but to a lesser degree, with human protein mda-7.[34] a protein that has antiproliferative properties in human melanoma cells. Mda-7 contains only two of the four cysteines of IL-10.
Interleukin 11 (IL-11) is a secreted protein that stimulates megakaryocytopoiesis, initially thought to lead to an increased production of platelets (it has since been shown to be redundant to normal platelet formation), as well as activating osteoclasts, inhibiting epithelial cell proliferation and apoptosis, and inhibiting macrophage mediator production. These functions may be particularly important in mediating the hematopoietic, osseous and mucosal protective effects of interleukin 11.[35]
Interleukin 12 (IL-12) is a disulphide-bonded heterodimer consisting of a 35kDa alpha subunit and a 40kDa beta subunit. It is involved in the stimulation and maintenance of Th1 cellular immune responses, including the normal host defence against various intracellular pathogens, such as Leishmania, Toxoplasma,Measles virus, andHuman immunodeficiency virus 1 (HIV). IL-12 also has an important role in enhancing the cytotoxic function ofNK cells[36][37] and role in pathological Th1 responses, such as in inflammatory bowel disease and multiple sclerosis. Suppression of IL-12 activity in such diseases may have therapeutic benefit. On the other hand, administration of recombinant IL-12 may have therapeutic benefit in conditions associated with pathological Th2 responses.[38][39]
Interleukin 13 (IL-13) is a pleiotropic cytokine that may be important in the regulation of the inflammatory and immune responses.[40] It inhibits inflammatory cytokine production and synergises with IL-2 in regulating interferon-gamma synthesis. The sequences of IL-4 and IL-13 are distantly related.[41]
Interleukin 15 (IL-15) is a cytokine that possesses a variety of biological functions, including stimulation and maintenance of cellular immune responses.[42] IL-15 stimulates the proliferation of T lymphocytes, which requires interaction of IL-15 with IL-15R alpha and components of IL-2R, including IL-2R beta and IL-2R gamma (common gamma chain, γc), but not IL-2R alpha.
Interleukin 17 (IL-17) is a potent proinflammatory cytokine produced by activated memory T cells.[43] This cytokine is characterized by its proinflammatory properties, role in recruiting neutrophils, and importance in innate and adaptive immunity. Not only does IL-17 play a key role in inflammation of many autoimmune diseases, such as RA, allergies, asthma, psoriasis, and more, but it also plays a key role in the pathogenesis of these diseases. Additionally, some studies have found that IL-17 plays a role in tumorigenesis (initial formation of a tumor) and transplant rejection.[44] The IL-17 family is thought to represent a distinct signaling system that appears to have been highly conserved across vertebrate evolution.[43]
| Name | Source[45] | Targets | Function[45] | |
|---|---|---|---|---|
| Receptors[45][46] | Cells[45] | |||
| IL-1 | macrophages,B cells,monocytes,[47]dendritic cells[47] | CD121a/IL1R1,CD121b/IL1R2 | T helper cells | co-stimulation[47] |
| B cells | maturation and proliferation[47] | |||
| NK cells | activation[47] | |||
| macrophages,endothelium, other | inflammation,[47] small amounts induceacute phase reaction, large amounts inducefever | |||
| IL-2 | Th1-cells | CD25/IL2RA,CD122/IL2RB,CD132/IL2RG | activated[47]T cells andB cells,NK cells,macrophages,oligodendrocytes | stimulates growth and differentiation of T cell response. Can be used inimmunotherapy to treat cancer or suppressed for transplant patients. Has also been used in clinical trials (ESPIRIT. Stalwart) to raise CD4 counts in HIV positive patients. |
| IL-3 | activatedT helper cells,[47]mast cells,NK cells,endothelium,eosinophils | CD123/IL3RA,CD131/IL3RB | hematopoietic stem cells | differentiation and proliferation of myeloid progenitor cells[47] to e.g.erythrocytes,granulocytes |
| mast cells | growth andhistamine release[47] | |||
| IL-4 | Th2 cells, just activated naiveCD4+ cell,memory CD4+ cells,mast cells,macrophages | CD124/IL4R,CD132/IL2RG | activatedB cells | proliferation and differentiation,IgG1 andIgE synthesis.[47] Important role inallergic response (IgE) |
| T cells | proliferation[47] | |||
| endothelium | increase expression ofvascular celladhesion molecule (VCAM-1) promoting adhesion of lymphocytes.[48] | |||
| IL-5 | Th2 cells,mast cells,eosinophils | CD125/IL5RA,CD131/IL3RB | eosinophils | production |
| B cells | differentiation,IgA production | |||
| IL-6 | macrophages,Th2 cells,B cells,astrocytes,endothelium | CD126/IL6RA,CD130/IL6RB | activatedB cells | differentiation intoplasma cells |
| plasma cells | antibody secretion | |||
| hematopoietic stem cells | differentiation | |||
| T cells, others | inducesacute phase reaction,hematopoiesis,differentiation,inflammation | |||
| IL-7 | Bone marrow stromal cells andthymus stromal cells | CD127/IL7RA,CD132/IL2RG | pre/pro-B cell,pre/pro-T cell, NK cells | differentiation and proliferation of lymphoid progenitor cells, involved in B, T, and NK cell survival, development, and homeostasis, ↑proinflammatory cytokines |
| IL-8 or CXCL8 | macrophages,lymphocytes,epithelial cells, endothelial cells | CXCR1/IL8RA,CXCR2/IL8RB/CD128 | neutrophils,basophils, lymphocytes | Neutrophilchemotaxis |
| IL-9 | Th2 cells, specifically by CD4+ helper cells | CD129/IL9R | T cells,B cells | PotentiatesIgM,IgG,IgE, stimulatesmast cells |
| IL-10 | monocytes,Th2 cells,CD8+ T cells,mast cells,macrophages,B cell subset | CD210/IL10RA,CDW210B/IL10RB | macrophages | cytokine production[47] |
| B cells | activation[47] | |||
| mast cells | ||||
| Th1 cells | inhibitsTh1 cytokine production (IFN-γ,TNF-β,IL-2) | |||
| Th2 cells | Stimulation | |||
| IL-11 | bone marrow stroma | IL11RA | bone marrow stroma | acute phase protein production,osteoclast formation |
| IL-12 | dendritic cells,B cells,T cells,macrophages | CD212/IL12RB1,IR12RB2 | activated[47]T cells, | differentiation intoCytotoxic T cells with IL-2,[47] ↑IFN-γ,TNF-α, ↓ IL-10 |
| NK cells | ↑IFN-γ,TNF-α | |||
| IL-13 | activatedTh2 cells,mast cells,NK cells | IL13R | Th2 cells, B cells, macrophages | Stimulates growth and differentiation ofB cells (IgE), inhibitsTh1 cells and the production ofmacrophage inflammatory cytokines (e.g. IL-1, IL-6), ↓ IL-8, IL-10, IL-12 |
| IL-14 | T cells and certain malignant B cells | activated B cells | controls the growth and proliferation ofB cells, inhibits Ig secretion | |
| IL-15 | mononuclear phagocytes (and some other cells), especially macrophages following infection by virus(es) | IL15RA | T cells, activated B cells | Induces production ofNatural killer cells |
| IL-16 | lymphocytes, epithelial cells, eosinophils, CD8+ T cells | CD4 | CD4+ T cells (Th-cells) | CD4+ chemoattractant |
| IL-17 | T helper 17 cells (Th17) | CDw217/IL17RA,IL17RB | epithelium, endothelium, other | osteoclastogenesis,angiogenesis, ↑ pro-inflammatorycytokines |
| IL-18 | macrophages | CDw218a/IL18R1 | Th1 cells, NK cells | Induces production ofIFN-γ, ↑ NK cell activity |
| IL-19 | - | IL20R | - | |
| IL-20 | Activated keratinocytes and monocytes | IL20R | regulates proliferation and differentiation ofkeratinocytes | |
| IL-21 | activated T helper cells, NKT cells | IL21R | All lymphocytes, dendritic cells | costimulates activation and proliferation of CD8+ T cells, augment NK cytotoxicity, augments CD40-driven B cell proliferation, differentiation and isotype switching, promotes differentiation of Th17 cells |
| IL-22 | T helper 17 cells (Th17) | IL22R | Production of defensins from epithelial cells.[36] ActivatesSTAT1 andSTAT3 and increases production ofacute phase proteins such asserum amyloid A,Alpha 1-antichymotrypsin andhaptoglobin inhepatoma cell lines | |
| IL-23 | macrophages,dendritic cells | IL23R | Maintenance of IL-17 producing cells,[36] increasesangiogenesis but reducesCD8 T-cell infiltration | |
| IL-24 | melanocytes,keratinocytes,monocytes, T cells | IL20R | Plays important roles intumor suppression, wound healing andpsoriasis by influencing cell survival, inflammatory cytokine expression. | |
| IL-25 | T Cells,mast cells,eosinophils,macrophages, mucosal epithelial cells | LY6E | Induces the productionIL-4,IL-5 andIL-13, which stimulateeosinophil expansion | |
| IL-26 | T cells,monocytes | IL20R1 | Enhances secretion ofIL-10 andIL-8 and cell surface expression ofCD54 onepithelial cells | |
| IL-27 | macrophages,dendritic cells | IL27RA | Regulates the activity ofB lymphocyte andT lymphocytes | |
| IL-28 | - | IL28R | Plays a role in immune defense againstviruses | |
| IL-29 | - | Plays a role in host defenses againstmicrobes | ||
| IL-30 | - | Forms one chain ofIL-27 | ||
| IL-31 | Th2 cells | IL31RA | May play a role ininflammation of theskin | |
| IL-32 | - | Induces monocytes and macrophages to secreteTNF-α,IL-8 andCXCL2 | ||
| IL-33 | epithelial cells | Induceshelper T cells to producetype 2 cytokine | ||
| IL-35 | regulatory T cells | Suppression of T helper cell activation | ||
| IL-36 | - | RegulatesDC andT cell responses | ||
| Endogenous form name | Pharmaceutical formINN suffix | INNs |
|---|---|---|
| interleukin-1 (IL-1) | -nakin | |
| interleukin-1α (IL-1α) | -onakin | pifonakin |
| interleukin-1β (IL-1β) | -benakin | mobenakin |
| interleukin-2 (IL-2) | -leukin | adargileukin alfa,aldesleukin,celmoleukin,denileukin diftitox,pegaldesleukin,teceleukin,tucotuzumab celmoleukin |
| interleukin-3 (IL-3) | -plestim | daniplestim,muplestim |
| interleukin-4 (IL-4) | -trakin | binetrakin |
| interleukin-6 (IL-6) | -exakin | atexakin alfa |
| interleukin-8 (IL-8) | -octakin | emoctakin |
| interleukin-10 (IL-10) | -decakin | ilodecakin |
| interleukin-11 (IL-11) | -elvekin | oprelvekin |
| interleukin-12 (IL-12) | -dodekin | edodekin alfa |
| interleukin-13 (IL-13) | -tredekin | cintredekin besudotox |
| interleukin-18 (IL-18) | -octadekin | iboctadekin |
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