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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:
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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, hematopoietic and embryonal development of an organism. Unlike hormones, cytokines are not stored in glands as pre-formed 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 (Ref. 1).
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:
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).
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. 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 T-cells and promote the initiation of T-cell responses (Ref. 6).
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).
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