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INTERFERON GAMMA
Valentina Grosso
The Inteferons
1957: Isaacs and Lindenmann discovered a substance that protected cells from viral infection
Interferon (IFN)
- Found only in vertebrates; small proteins 143 - 172 aa ranging from 19 to 45 kDa, modified by glycosylation; - Prototypes for the clinical development of other cytokines; - Their metabolism and excretion take place mainly in the liver and kidneys. They rarely pass the placenta and the blood brain barrier; - Synthesized when induced by viral or other challenges by specialized cells, subsequently secreted, and bind to highly specific receptors on target cells. This specific interaction with its receptors causes the signal transduction to the nucleus and thus regulates the production of about 50 different genes; - Interferons are a group of cytokines with important activities: - immunomodulatory - antiviral leukocytes - antiangiogenic - antiproliferative HPLC fibroblasts - antitumor immune cells: - NK, - T lymphocytes (CD4+, CD8+ cells)
Types of interferons
Takaoka A. et al., Interferon signalling network in innate defence, Cellular Microbiology, 8:907, 2006
IFN- : - strongly produced by activated T cells, macrophages or NK cells; - drives expression of MHC class II on antigen presenting cells; - increases chemokine secretion; - activates macrophages, lymphocytes and endothelial cells; - promotes the differentiation of naive helper T cells into Th1 cells; - activates polymorphonuclear leukocytes (PMN) and cytotoxic T cells and increases the cytotoxicity of NK cells.
Bowers W., Microbiology and Immunology on-line, Immunology chapter 12 fig.8
http: //www.ncbi.nlm.nih.gov/Structure/
Evolution of IFN-
IFN- has been maintained as a single gene with presumably constant function and evolutionary pressure
No homolog of IFN- has been observed in frogs and in fish genomes, implying that type II IFN function became essential during tetrapod evolution, though its origin may be considerably earlier.
Pestka S. et al., Interferons, interferon-like cytokines, and their receptors, Immunological R eviews, 202:8, 2004
activation macrophages
(macrophage-infiammatory protein-1)
polarise T cell development towards a Th1 phenotype potentiate IFN secretion by NK or T cells in sites of inflammation produce IFN
IFN IS A PRO-INFLAMMATORY CYTOKINE, INTIMATELY INVOLVED IN THE INNATE AND ACQUIRED IMMUNE RESPONSES
IFN is a pro-inflammatory cytokine, intimately involved in the innate and acquired immune responses:
IFN constitutes a warning signal produced by the host, and participates in an amplification loop to rapidly alert neighbouring cells, as well as effector cells of the innate immune system, to possible infection. IFN signalling: - upregulation of pathogen recognition; - induction of an antiviral state; - inhibition of cellular proliferation and modulation of apoptosis; - acquisition of microbicidal effector functions. One of the most important functions of IFN is to sensitise macrophages to activation by challenge with pathogen products. Indeed, IFN was originally named macrophage - activating factor.
Patients with inactivating mutations of the human IFNGR1 or IFNGR2 chains and IFN -/-and IFNGR1-/- mice showed no developmental defects, and their immune system appeared to develop normally, but these patients show deficiencies in natural resistance to bacterial, parasitic, and viral infections.
Infants with deficient production of IFN exhibited decreased neutrophil mobility and NK cell activity, highlighting the importance of IFN in the inflammatory response and immunoregulation. His function is significant in tumor surveillance and also as IFN- is vitally implicated in the regulation of immune response, its production can lead to autoimmune disorders.
IL12 production
positive feedback
Schroder K. et al., Interferon- :an overview of signals, mechanisms and functions, Journal of Leukocyte Biology, 75:163, 2004
Schroder K. et al., Interferon- :an overview of signals, mechanisms and functions, Journal of Leukocyte Biology, 75:163, 2004
Brandacher G. et al., Antitumoral Activity of Interferon- Involved in Impaired Immune Function in Cancer Patients, Current Drug Metabolism, 7:599, 2006
Indoleamine 2,3 dioxygenase (IDO) IDO is rate-limiting enzyme in the degradation of the essential amino acid tryptophan via the kynurenine pathway to form N-formyl-kynurenine, which is subsequently converted to niacin. Thereby, growth of microbes and tumor cells is affected, because tryptophan deprivation limits protein biosynthesis. IDO is expressed, particularly by IFN, in multiple cell types: - fibroblasts - macrophages - DC - trophoblasts - epithelial cells For many years has been considered as an innate defence mechanism limiting growth of viruses, bacteria, intracellular pathogens and malignant cells by withdrawing tryptophan from the microenvironment. Recently, it has been shown that activation of IDO is also critically involved in the regulation of immune responses. If the immune system is unable to eliminate the malignant tumor cells, immune activation may persist, which causes overproduction of IFN-. One consequence for these detrimental IFN- effects might be increased tryptophan depletion, which can affect T-cell responses and thus contribute to the development of immunodeficiency in cancer patients.
When the acute immune response cascade has failed to completely destroy foreign tissue structures, the anti-proliferative enzyme systems (the degradation of tryptophan by IDO, the production of ROS, of NO and ONOO-) are chronically up-regulated by IFN together with TNF-. Moreover, cancer cells stimulated by the cytokines themselves become a relevant source of tryptophan degradation. As a consequence also metabolism of normal cells more and more begins to suffer from symptoms linked with IFN over-expression namely anemia, cachexia, depression, immunodeficiency and higher risk of infection and sepsis. Although IFN- is a central pro-inflammatory cytokine, evidence increasingly indicates that it is also involved in the development of tumor immune escape, tolerance induction and impaired immune functions by activating a negative feedback loop.
Brandacher G. et al., Antitumoral Activity of Interferon- Involved in Impaired Immune Function in Cancer Patients, Current Drug Metabolism, 7:599, 2006
BIBLIOGRAFIA
Pestka S. et al., Interferons, interferon-like cytokines, and their receptors, Immunological Reviews, 202:8, 2004 Parmar S. et al., Interferons: mechanisms of action and clinical applications, CurrOpinOncol,15:431,2003 Takaoka A. et al., Interferon signalling network in innate defence, Cellular Microbiology, 8:907, 2006 Ghosh S. et al., Interfering with interferons in inflammatory bowel disease, Gut, 55:1071, 2006 Platanias L.C., Mechanisms of type-I- and type-II-interferon-mediated signalling, Nature Reviews Immunology, 5:375, 2005 Schroder K. et al., Interferon- :an overview of signals, mechanisms and functions, Journal of Leukocyte Biology, 75:163, 2004 Schroder K. et al., Signal integration between IFN and TLR signalling pathways in macrophages, Immunobiology, 211:511, 2006 Szabo S.J. Et al, Distinct Effects of T-bet in TH1 Lineage Commitment and IFN- Production in CD4 and CD8 T Cells, Science, 295:338, 2002 Foulds K.E. et al., Th1 memory: implications for vaccine development, Immunological Reviews, 211:58, 2006 Bogdan C. et al., Production of interferon- by myeloid cells fact or fancy?, TRENDS in Immunology , 27:282, 2006 Brandacher G. et al., Antitumoral Activity of Interferon- Involved in Impaired Immune Function in Cancer Patients, Current Drug Metabolism, 7:599, 2006