Product Categories

Cytokine Network

The immune system recognizes the presence of pathogens by several proteins that bind to molecules secreted by the pathogen or carried on their surface. The cells responsible for these immune responses include the B-Cells, T-Cells, macrophages, neutrophils, basophils, eosinophils, endothelial cells, or mast cells (Ref.1). These cells have distinct roles in the immune system, and communicate with other immune cells by cytokines, which control proliferation, differentiation and function of cells of the immune system. Furthermore, they are involved in processes of inflammation and in the neuronal, haematopoietic and embryonal development of an organism. Unlike hormones, cytokines are not stored in glands as preformed molecules, but are rapidly synthesized and secreted by different cells mostly after stimulation. Cytokines are pleiotropic in their biological activities and play pivotal roles in a variety of responses, including the immune response, hematopoiesis, neurogenesis, embryogenesis, and oncogenesis. They frequently affect the action of other cytokines in an additive, synergistic or antagonistic manner.
 
Cytokines have been classified on the basis of their biological responses into pro- or anti-inflammatory cytokines, depending on their effects on immunocytes (Ref.2). Cytokines act in networks or cascades. Major cytokines include the ILs (Interleukins), Growth Hormone, IFN (Interferons) and TNFs (Tumor Necrosis Factors-Alpha and Beta). Many of the cytokines act locally like autocrine hormones and their targets are cells of the same or similar type as the cytokine-producing cell. A characteristic that significantly differentiates some of the cytokines from hormones is the coupling of their activity to cell-cell interactions. The function of some cytokines such IL-1, IL-2, IL-4, IL-5, IL-6 and IL-10 is closely associated with the interactions between B-Cells and T-Cells (Ref.3). IL-1 activates Antigen Presenting Cell and CD4+ lymphocytes; affect the differentiation of the B-Cells and T-Cells and other immunocompetent cells and takes part in the regulation of productions of other cytokines and GMCSF (Granulocyte-Macrophage Colony-Stimulating Factor) (Ref.6). IL-2 stimulates the proliferation and activation of B-Cells and T-Cells. IL-4 plays a role in the differentiation of TH2 (T Helper Type-2), in allergic responses, and in the switching of antibody types. IL-5 stimulates the production and maturation of eosinophils during inflammation. IL-8 acts as a chemotactic factor that attracts neutrophils, basophils and T-Cells to sites of inflammation. IL-12 is a critical linker between the innate immunity and adaptive immunity, capable of TH1 (T Helper Type-1) differentiation and IFN-Gamma release by T-Cells and NK cells (Ref.4). IL-10 acts to repress secretion of pro-inflammatory cytokines. IL-3 is a poly potent activator of the hemopoietic cells. It stimulates NK-Cells and acts as a synergist with IL-4 during the induction of CD4+ lymphocyte activation process. IL-7 is known as the growth factor of the immature B-Cells and T-Cells. It induces apoptosis of tumor cells and causes differentiation of cells from a subgroup of acute myeloblastic leukemia. IL-9 stimulates the excretion of IL-2, IL-4, IL-6, IL-11, and takes part in a stimulation of cytotoxicity of T-killers and NK-Cells, inducing apoptosis. IL-11 is a pro-inflammative factor, which regulates the functions of B-Cells and T-Cells. It also takes part in the induction of various killer cells' activities and acts as an autocrine factor for the proliferation of megacaryocytes. IL-13 is very sensitive to the monocytes and B-Cells. IL-13 does not act on T-Cells but inhibits the proliferation of leukemic pro-B-Cells. IL-14 is a BCGF (B-Cell Growth Factor) and the hyper production of this interleukin enables the progression of NHL-B (B-cell Type Non Hodgkin's lymphoma). IL-15, in the biological properties, is very much analogous to IL-2 and increases the antitumor activities of T-killers and NK-Cells, and the production of cytokines CD4+ lymphocytes. IL-17 is principally produced by CD4+ T-Cells, which induces granulopoiesis via GMCSF. It takes part in the regulation of many cytokines and can reinforce the antibody dependant tumor cell destructions. IL-18 acts as a synergist with IL-12 in some of their effects, especially in the induction of IFN-Gamma production and inhibition of angiogenesis. IL-19 is produced mainly by monocytes and in its biological function is similar to IL-10. It is stimulated by GMCSF and regulates the functions of macrophages, and also suppresses the activities of TH1 and TH2. IL-21 executes an important role in the regulation of haematopoiesis and immune response. It promotes a high production of T-Cells, fast growth and maturation of NK-Cells and B-Cells population. IL-22 is produced by activated T-Cells in an acute stage of inflammation. In its bioactivities, it is similar to IL-10, but does not prohibit the production of pro-inflammatory cytokines through monocytes (Ref.1). The complex interplay of these different cytokine functions with immune cells is essential for correct immune function.
 
In addition to the above cytokines, the release of other inflammatory cytokines, particularly TNFs (TNF-Alpha and TNF-Beta) from mast cells and the associated recruitment of neutrophils are an important component of the protective action of mast cells against infestation. The secretion of TNF-Alpha and TNF-Beta by TH1 cells activates macrophages, inhibits apoptosis of neutrophils and eosinophils, and induces vascular endothelial cells at the sites of infection to change the adhesion molecules they express so phagocytes circulating in the blood can bind to them (Ref.6). IFN-Alpha, IFN-Beta and IFN-Gamma are produced in the area of infection during the early phase of immune response. IFN-Alpha and IFN-Beta induce proliferation of NK-Cells and stimulate innate and adaptive immune responses that are specifically targeted to virus infections. Upon activation NK cells release IFN-Gamma, which activates macrophages to secrete cytokines that help to activate macrophages to secrete cytokines that help to activate T-Cells and promote the initiation of T-Cell responses.
 
Cytokines play an important role in the communication between cells of multicellular organisms. As intercellular mediators, they regulate survival, growth, differentiation and effector functions of cells. Besides their pleiotropic effects, cytokine actions are often redundant and they exert their actions, which can be auto-, para- or endocrine, via specific cell-surface receptors on their target cells (Ref.2). They are key players in the regulation of the immune response, particularly during infections, inflammatory joint, kidney, vessel and bowel diseases, or neurological and endocrinological autoimmune diseases (Ref.5).
 
References:
 
1.Comparison of serum and cell-specific cytokines in humans. 
Stanley AC, Lacy P.
Physiology (Bethesda). 2010 Aug;25(4):218-29.
 
2.Analytic review: Interleukin-6 in surgery, trauma, and critical care: part I: basic science.
Jawa RS, Anillo S, Huntoon K, Baumann H, Kulaylat M.
J Intensive Care Med. 2011 Jan-Feb;26(1):3-12.
 
3.Chemokine RANTES/CCL5 as an unknown link between wound healing in the jawbone and systemic disease: is prediction and tailored treatments in the horizon?
Lechner J, von Baehr V.
EPMA J. 2015 May 6;6(1):10. doi: 10.1186/s13167-015-0032-4. eCollection 2015.
 
4.Current status of the immunomodulation and immunomediated therapeutic strategies for multiple sclerosis.
Chen SJ, Wang YL, Fan HC, Lo WT, Wang CC, Sytwu HK.
Clin Dev Immunol. 2012;2012:970789. Epub 2011 Dec 6.
 
5.Molecular basis for shared cytokine recognition revealed in the structure of an unusually high affinity complex between IL-13 and IL-13Ralpha2 
Lupardus PJ, Birnbaum ME, Garcia KC.
Structure. 2010 Mar 10;18(3):332-42.
 
6.Differentiation of effector CD4 T cell populations.
Zhu J, Yamane H, Paul WE.
Annu Rev Immunol. 2010 Mar;28:445-89.