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| | ==Innate immunity== | | ==Innate immunity== |
| | This becomes active during the early stages of infection. Defences include: | | This becomes active during the early stages of infection. Defences include: |
| − | *Interferon (IFN) - typically stimulates the inhibition of viral replication. There are three known types: | + | *[[Cytokines|Interferon (IFN)]] - typically stimulates the inhibition of viral replication. There are three known types: |
| | **Infection of a cell by a virus stimulates production of IFN-α and IFN-β, which activate genes in neighbouring cells. One of these genes, for example, codes for a protein kinase that blocks translation of proteins. Another activates an endonuclease that degrades viral RNA. | | **Infection of a cell by a virus stimulates production of IFN-α and IFN-β, which activate genes in neighbouring cells. One of these genes, for example, codes for a protein kinase that blocks translation of proteins. Another activates an endonuclease that degrades viral RNA. |
| | **IFN-γ increases the expression of MHC I and II, enhancing the function of the adaptive immune response. It also activates macrophages and NK cells. | | **IFN-γ increases the expression of MHC I and II, enhancing the function of the adaptive immune response. It also activates macrophages and NK cells. |
| − | *Natural killer (NK) cells- one of the main mediators of antibody-dependent cell-mediated cytotoxicity | + | *[[Natural Killer cells|Natural killer (NK) cells]] - one of the main mediators of antibody-dependent cell-mediated cytotoxicity |
| | *For more on [[Innate Immunity to Viruses|Innate immunity to viruses]], see here. | | *For more on [[Innate Immunity to Viruses|Innate immunity to viruses]], see here. |
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| | [[Image:B Cell viral response.jpg|thumb|right|200px|B Cell Immunity to Viruses - B. Catchpole, RVC 2008]] | | [[Image:B Cell viral response.jpg|thumb|right|200px|B Cell Immunity to Viruses - B. Catchpole, RVC 2008]] |
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| − | *[[Immunoglobulin|Antibodies]] - these are particularly important in preventing the spread of the virus in the bloodstream | + | *[[Immunoglobulins|Antibodies]] - these are particularly important in preventing the spread of the virus in the bloodstream |
| | **[[IgA]] production is increased at mucosal surfaces- helps prevent reinfection | | **[[IgA]] production is increased at mucosal surfaces- helps prevent reinfection |
| | **Although antibodies that target any viral protein can be produced, only those directed against proteins found in the virion envelope or infected cell membrane will be effective | | **Although antibodies that target any viral protein can be produced, only those directed against proteins found in the virion envelope or infected cell membrane will be effective |
| | **When targeted against free virus particles, antibodies are effective at preventing them binding and entering the cell and uncoating. | | **When targeted against free virus particles, antibodies are effective at preventing them binding and entering the cell and uncoating. |
| − | **When targeting virus-infected cells, they aid antibody-dependent cell-mediated cytotoxicity by NK cells, macrophages and [[Neutrophils|neutrophils]] | + | **When targeting virus-infected cells, they aid antibody-dependent cell-mediated cytotoxicity by NK cells, [[Macrophages|macrophages]] and [[Neutrophils|neutrophils]] |
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| | *[[Complement]] - although not considered a major factor in defence against viruses, complement is able to damage the virion envelope (virolysis) | | *[[Complement]] - although not considered a major factor in defence against viruses, complement is able to damage the virion envelope (virolysis) |
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| | ***aid opsonisation of free virus or infected cells for phagocytosis | | ***aid opsonisation of free virus or infected cells for phagocytosis |
| | [[Image:T Cell viral response.jpg|thumb|right|200px|T Cell Immunity to Viruses - B. Catchpole, RVC 2008]] | | [[Image:T Cell viral response.jpg|thumb|right|200px|T Cell Immunity to Viruses - B. Catchpole, RVC 2008]] |
| − | *T cells | + | *[[T cells]] |
| | **CD8<sup>+</sup> cytotoxic T cells are particularly important as nearly all the cells in the body express MHC class I. They tend to focus at the site of viral replication and destroy virus-infected cells. | | **CD8<sup>+</sup> cytotoxic T cells are particularly important as nearly all the cells in the body express MHC class I. They tend to focus at the site of viral replication and destroy virus-infected cells. |
| | **CD4<sup>+</sup> T cells are important in the recruitment of macrophages, using cytokines such as IFN-γ and TNF, and the induction of CD8<sup>+</sup> cytotoxic T cells | | **CD4<sup>+</sup> T cells are important in the recruitment of macrophages, using cytokines such as IFN-γ and TNF, and the induction of CD8<sup>+</sup> cytotoxic T cells |