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Interleukin-12 is produced by macrophages, neutrophils, and some B cells. Il-12 helps make cytotoxic cells and natural killer cells. T cells turn into cytotoxic t cells when il-12 is released. It helped to generate cell mediated immunity. When it makes the cells they are cytotoxic so they kill more cells that are infected by a pathogen.
Interleukin-12 is produced by macrophages, neutrophils, and some B cells. Il-12 helps make cytotoxic cells and natural killer cells. T cells turn into cytotoxic t cells when il-12 is released. It helped to generate cell mediated immunity. When it makes the cells they are cytotoxic so they kill more cells that are infected by a pathogen.
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Innate immunity is when the body has defense mechanisms that starts working within hours of a pathogen being introduced into the body. Innate is the first line of defense against pathogens so there is no specific pathogen they attack anything. Adaptive immunity is acquired or specific. Each attack is specific to the pathogen. It is supposed to attack pathogens that are invading. If it attacks its own pathogens it can form autoimmune disorders. Adaptive immunity is done by b or t lymphoctyes. T helper cells secrete different cytokines like il-12 which lets il-12 activate innate natural killer cells and adaptive cytotoxic t cells. Il-12 helps mature cytotoxic t cells so they can attack specific pathogens. It also helps stimulate the production of natural killer cells so they can start innate immunity. Il-12 is produced by dendritic cells, and monocytes.
Innate immunity is when the body has defense mechanisms that starts working within hours of a pathogen being introduced into the body. Innate is the first line of defense against pathogens so there is no specific pathogen they attack anything. Adaptive immunity is acquired or specific. Each attack is specific to the pathogen. It is supposed to attack pathogens that are invading. If it attacks its own pathogens it can form autoimmune disorders. Adaptive immunity is done by b or t lymphoctyes. T helper cells secrete different cytokines like il-12 which lets il-12 activate innate natural killer cells and adaptive cytotoxic t cells. Il-12 helps mature cytotoxic t cells so they can attack specific pathogens. It also helps stimulate the production of natural killer cells so they can start innate immunity. Il-12 is produced by dendritic cells, and monocytes.
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To increase the production of il-12 it can be done through priming or amplification. In priming when it binds to a ligand and goes through the toll like receptors it allows more il-12 to pass through faster. Amplification happens through a cytokine network where different cytokines are secreted through different cells.
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Il-12 has many action. One action is stimulating the growth and cytotoxicity of natural killer cells. They also convert th0 cells into th1 cells by activating specific transcription factors. Il-12 also stimulated the production of interferon gamma (1hig) which is another type of cytokine used in innate and adaptive immunity. It is secreted by t cells and natural killer cells also. It promotes macrophage activation meaning it helps more macrophages to be activated so it can eat bacteria, viruses, and fungi. Il-12 also helped to introduce IgG and suppress IgE from B cells. IgG is an antibody released from plasma B cells and has two antigen binding sites. It also is the most abundant antibody and helps to fight bacterial and viral infects. IgE is an antibody that is produced when your immune system reacts to an allergen. All those actions that il-12 performs helps it with its antitumor effects. In animal studies il-12 has been useful in tumor therapy. Its effectiveness is also increased when used with other therapeutic models.
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To increase the production of il-12 it can be done through priming or amplification. In priming when it binds to a ligand and goes through the toll like receptors it allows more il-12 to pass through faster. Amplification happens through a cytokine network where different cytokines are secreted through different cells.
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Il-12 is proinflammatory meaning it promotes inflammation which contributes in developing th1 cells from th0 cells. It also participates in a positive feed back loop. Il-12 caused interferon gamma production from t cells. That facilitated th1 differentiation. Il-12 also induced production of interferon gamma by natural killer cells. Interferon gamma can be a part of the positive feed back loop because transcription factors are activated. In a study done on mice if specific transcription factors are not expressed than there can be a defect in one or both subunits of il-12.
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Il-12 has many actions. One action is stimulating the growth and cytotoxicity of natural killer cells. They also convert th0 cells into th1 cells by activating specific transcription factors. Il-12 also stimulated the production of interferon gamma (1hig) which is another type of cytokine used in innate and adaptive immunity. It is secreted by t cells and natural killer cells also. It promotes macrophage activation meaning it helps more macrophages to be activated so it can eat bacteria, viruses, and fungi. Il-12 also helped to introduce IgG and suppress IgE from B cells. IgG is an antibody released from plasma B cells and has two antigen binding sites. It also is the most abundant antibody and helps to fight bacterial and viral infects. IgE is an antibody that is produced when your immune system reacts to an allergen. All those actions that il-12 performs helps it with its antitumor effects. In animal studies il-12 has been useful in tumor therapy. Its effectiveness is also increased when used with other therapeutic models.
 +
 
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Il-12 is proinflammatory meaning it promotes inflammation which contributes in developing th1 cells from th0 cells. It also participates in a positive feed back loop. Il-12 caused interferon gamma production from t cells. That facilitated th1 differentiation. Il-12 also induced production of interferon gamma by natural killer cells. Interferon gamma can be a part of the positive feed back loop because transcription factors are activated. In a study done on mice if specific transcription factors are not expressed than there can be a defect in one or both subunits of il-12.

Revision as of 17:43, 27 April 2020

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References

[4] [5]

  1. Hanson, R. M., Prilusky, J., Renjian, Z., Nakane, T. and Sussman, J. L. (2013), JSmol and the Next-Generation Web-Based Representation of 3D Molecular Structure as Applied to Proteopedia. Isr. J. Chem., 53:207-216. doi:http://dx.doi.org/10.1002/ijch.201300024
  2. Herraez A. Biomolecules in the computer: Jmol to the rescue. Biochem Mol Biol Educ. 2006 Jul;34(4):255-61. doi: 10.1002/bmb.2006.494034042644. PMID:21638687 doi:10.1002/bmb.2006.494034042644
  3. Lasek W, Zagozdzon R, Jakobisiak M. Interleukin 12: still a promising candidate for tumor immunotherapy? Cancer Immunol Immunother. 2014 May;63(5):419-35. doi: 10.1007/s00262-014-1523-1., Epub 2014 Feb 11. PMID:24514955 doi:http://dx.doi.org/10.1007/s00262-014-1523-1
  4. Lasek W, Zagozdzon R, Jakobisiak M. Interleukin 12: still a promising candidate for tumor immunotherapy? Cancer Immunol Immunother. 2014 May;63(5):419-35. doi: 10.1007/s00262-014-1523-1., Epub 2014 Feb 11. PMID:24514955 doi:http://dx.doi.org/10.1007/s00262-014-1523-1
  5. Yoon C, Johnston SC, Tang J, Stahl M, Tobin JF, Somers WS. Charged residues dominate a unique interlocking topography in the heterodimeric cytokine interleukin-12. EMBO J. 2000 Jul 17;19(14):3530-41. PMID:10899108 doi:http://dx.doi.org/10.1093/emboj/19.14.3530

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