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| |sublink2 =Adaptive Immune System - WikiBlood | | |sublink2 =Adaptive Immune System - WikiBlood |
| |subtext2 =ADAPTIVE IMMUNE SYSTEM | | |subtext2 =ADAPTIVE IMMUNE SYSTEM |
− | |sublink3=Lymphocytes - WikiBlood | + | |sublink3=Lymphocytes |
| |subtext3=LYMPHOCYTES | | |subtext3=LYMPHOCYTES |
| |pagetype =Blood | | |pagetype =Blood |
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| ==Introduction== | | ==Introduction== |
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− | Within the blood and lymphoid organs the majority of [[Lymphocytes - WikiBlood#Helper CD4+|CD4+ T cells]] are antigen-naive T-cells. There is only a small proportion of memory T-cells. | + | Within the blood and lymphoid organs the majority of [[Lymphocytes#Helper CD4+|CD4+ T cells]] are antigen-naive T-cells. There is only a small proportion of memory T-cells. |
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− | Naive T-cells have yet to encounter antigen and can only be activated by antigen presented by dendritic cells. After initial antigenic activation, naïve T-cells develop into an intermediate stage cell called the TH<sub>0</sub> cell which can then be activated by any antigen-presenting cell, e.g. Dendritic cells, [[Macrophages - WikiBlood|macrophages]] or [[Lymphocytes - WikiBlood#B cells|B-cells]]. | + | Naive T-cells have yet to encounter antigen and can only be activated by antigen presented by dendritic cells. After initial antigenic activation, naïve T-cells develop into an intermediate stage cell called the TH<sub>0</sub> cell which can then be activated by any antigen-presenting cell, e.g. Dendritic cells, [[Macrophages - WikiBlood|macrophages]] or [[Lymphocytes#B cells|B-cells]]. |
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− | The TH<sub>0</sub> cells have the capacity to differentiate into TH<sub>1</sub> and TH<sub>2</sub> cells. The type of cell that develops depends on the antigen presenting cell. [[Macrophages - WikiBlood|Macrophages]] cause the TH<sub>0</sub> cell to develop into TH<sub>1</sub> cells caused by IL-12 production following [[Macrophages - WikiBlood|macrophage]]-antigen interaction. [[Lymphocytes - WikiBlood#B cells|B-cells]] cause the TH<sub>0</sub> cell to develop into TH<sub>2</sub> cells caused by IL-10 production following B-cell-antigen interaction. On antigenic stimulation the TH<sub>1</sub> or TH<sub>2</sub> cells become activated, undergo clonal expansion and secrete a range of different cytokines. | + | The TH<sub>0</sub> cells have the capacity to differentiate into TH<sub>1</sub> and TH<sub>2</sub> cells. The type of cell that develops depends on the antigen presenting cell. [[Macrophages - WikiBlood|Macrophages]] cause the TH<sub>0</sub> cell to develop into TH<sub>1</sub> cells caused by IL-12 production following [[Macrophages - WikiBlood|macrophage]]-antigen interaction. [[Lymphocytes#B cells|B-cells]] cause the TH<sub>0</sub> cell to develop into TH<sub>2</sub> cells caused by IL-10 production following B-cell-antigen interaction. On antigenic stimulation the TH<sub>1</sub> or TH<sub>2</sub> cells become activated, undergo clonal expansion and secrete a range of different cytokines. |
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− | For any one cell the cytokine-secreting activation state is short-lived, lasting between 4 - 40 hours. After this time these cells either die, or mature into the long-lived memory cells. The proliferation of [[Lymphocytes - WikiBlood#T cells|T cells]] continues until antigen disappears. | + | For any one cell the cytokine-secreting activation state is short-lived, lasting between 4 - 40 hours. After this time these cells either die, or mature into the long-lived memory cells. The proliferation of [[Lymphocytes#T cells|T cells]] continues until antigen disappears. |
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| ==Dendritic Cells== | | ==Dendritic Cells== |
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| **From plasmacytoid precursor cells | | **From plasmacytoid precursor cells |
| *Stimulate a primary T cell response | | *Stimulate a primary T cell response |
− | *Migrate through tissues, track to [[Lymphocytes - WikiBlood#T cells|T cells]] dependent areas of [[Lymph Nodes - Anatomy & Physiology|lymph node]] and cluster with [[Lymphocytes - WikiBlood#T cells|T cells]] | + | *Migrate through tissues, track to [[Lymphocytes#T cells|T cells]] dependent areas of [[Lymph Nodes - Anatomy & Physiology|lymph node]] and cluster with [[Lymphocytes#T cells|T cells]] |
| *Dendritic cells have unique capabilities to take up antigen by pathways involving phagocytosis, macropinocytosis and clathrin-coated pits | | *Dendritic cells have unique capabilities to take up antigen by pathways involving phagocytosis, macropinocytosis and clathrin-coated pits |
− | *Cell-surface antigen phenotype distinguishing it from [[Monocytes - WikiBlood]]/macrophages and [[Lymphocytes - WikiBlood#B Cells|B cells]] | + | *Cell-surface antigen phenotype distinguishing it from [[Monocytes - WikiBlood]]/macrophages and [[Lymphocytes#B Cells|B cells]] |
| *Cell-surface expression pattern according to their differentiation/maturation/activation | | *Cell-surface expression pattern according to their differentiation/maturation/activation |
− | *Main function is priming of [[Lymphocytes - WikiBlood#T cells|T helper cells]] | + | *Main function is priming of [[Lymphocytes#T cells|T helper cells]] |
| *Produces [[Cytokines - WikiBlood#Chemokines|chemokines]] | | *Produces [[Cytokines - WikiBlood#Chemokines|chemokines]] |
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| ===Antigen Presentation by Dendritic Cells=== | | ===Antigen Presentation by Dendritic Cells=== |
− | *Dendritic cells present antigen to [[Lymphocytes - WikiBlood#T cells|T cells]] | + | *Dendritic cells present antigen to [[Lymphocytes#T cells|T cells]] |
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| *Circulating [[Monocytes - WikiBlood]] differentiate to form immature dendritic cells called '''Langerhans Cells''' | | *Circulating [[Monocytes - WikiBlood]] differentiate to form immature dendritic cells called '''Langerhans Cells''' |
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| *The Langerhans cells leave the epithelium and travel via the afferent lymph. They are now called '''Veiled Cells''' | | *The Langerhans cells leave the epithelium and travel via the afferent lymph. They are now called '''Veiled Cells''' |
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− | *Veiled cells enter the paracortical region of the [[Lymph Nodes - Anatomy & Physiology|lymph node]] where they present antigen to [[Lymphocytes - WikiBlood#T cells|T cells]]. They are now called '''Interdigitating Dendritic Cells''' | + | *Veiled cells enter the paracortical region of the [[Lymph Nodes - Anatomy & Physiology|lymph node]] where they present antigen to [[Lymphocytes#T cells|T cells]]. They are now called '''Interdigitating Dendritic Cells''' |
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| ==TH<sub>1</sub> Cells== | | ==TH<sub>1</sub> Cells== |
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| * Cytokines secreted include: | | * Cytokines secreted include: |
| ** '''IL-2'''. | | ** '''IL-2'''. |
− | *** Gives proliferation of both [[Lymphocytes - WikiBlood#Helper CD4+|CD4+]] and [[Lymphocytes - WikiBlood#Cytotoxic CD8+|CD8+ T-cells]]. | + | *** Gives proliferation of both [[Lymphocytes#Helper CD4+|CD4+]] and [[Lymphocytes#Cytotoxic CD8+|CD8+ T-cells]]. |
− | *** This stimulation of proliferation of [[Lymphocytes - WikiBlood#T cells|T cells]] is the main function of the TH<sub>1</sub> cell. | + | *** This stimulation of proliferation of [[Lymphocytes#T cells|T cells]] is the main function of the TH<sub>1</sub> cell. |
| ** '''Interferon gamma''' ('''IFNγ'''). | | ** '''Interferon gamma''' ('''IFNγ'''). |
| *** Activates tissue macrophages | | *** Activates tissue macrophages |
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| ==TH<sub>2</sub> Cells== | | ==TH<sub>2</sub> Cells== |
| [[Image:TH2-Bcell.jpg|thumb|right|150px|TH2 cells incite increased antibody production - B. Catchpole, RVC 2008]] | | [[Image:TH2-Bcell.jpg|thumb|right|150px|TH2 cells incite increased antibody production - B. Catchpole, RVC 2008]] |
− | *TH2 cells help [[Lymphocytes - WikiBlood#B cells|B cell]] produce antibody (''organism in tissue fluid'') | + | *TH2 cells help [[Lymphocytes#B cells|B cell]] produce antibody (''organism in tissue fluid'') |
− | * The TH2 population influences [[Lymphocytes - WikiBlood#B cells|B cell]] activation, proliferation and immunoglobulin production. | + | * The TH2 population influences [[Lymphocytes#B cells|B cell]] activation, proliferation and immunoglobulin production. |
− | * The TH2 [[Lymphocytes - WikiBlood#T cells|T cell]] population secrete a range of cytokines. | + | * The TH2 [[Lymphocytes#T cells|T cell]] population secrete a range of cytokines. |
| ** '''IL-4''' | | ** '''IL-4''' |
− | *** Stimulates [[Lymphocytes - WikiBlood#B cells|B cell]] growth. | + | *** Stimulates [[Lymphocytes#B cells|B cell]] growth. |
| *** Gives heavy chain switch from [[Immunoglobulin M - WikiBlood|IgM]] to [[Immunoglobulin G - WikiBlood|IgG]] , [[Immunoglobulin A - WikiBlood|IgA]] and [[Immunoglobulin E - WikiBlood|IgE]]. | | *** Gives heavy chain switch from [[Immunoglobulin M - WikiBlood|IgM]] to [[Immunoglobulin G - WikiBlood|IgG]] , [[Immunoglobulin A - WikiBlood|IgA]] and [[Immunoglobulin E - WikiBlood|IgE]]. |
| *** Proliferation of basophils/ mast cells. | | *** Proliferation of basophils/ mast cells. |
− | *** Can inhibit some [[Lymphocytes - WikiBlood#T cells|T cell]] responses. | + | *** Can inhibit some [[Lymphocytes#T cells|T cell]] responses. |
| ** '''IL-5''' | | ** '''IL-5''' |
− | *** Activates [[Lymphocytes - WikiBlood#B cells|B cells]]. | + | *** Activates [[Lymphocytes#B cells|B cells]]. |
− | *** Stimulates high rate [[Lymphocytes - WikiBlood#B cells|B cells]] proliferation. | + | *** Stimulates high rate [[Lymphocytes#B cells|B cells]] proliferation. |
| *** Promotes immunoglobulin synthesis. | | *** Promotes immunoglobulin synthesis. |
| *** Proliferation and differentiation of eosinophils. | | *** Proliferation and differentiation of eosinophils. |
| ** '''IL-6''' | | ** '''IL-6''' |
− | *** Activates [[Lymphocytes - WikiBlood#B cells|B cells]]. | + | *** Activates [[Lymphocytes#B cells|B cells]]. |
− | *** Stimulates high rate [[Lymphocytes - WikiBlood#B cells|B cell]] proliferation. | + | *** Stimulates high rate [[Lymphocytes#B cells|B cell]] proliferation. |
| *** Promotes immunoglobulin synthesis. | | *** Promotes immunoglobulin synthesis. |
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| * Viruses are intracellular pathogens that use the host cell machinery for pathogen protein synthesis. | | * Viruses are intracellular pathogens that use the host cell machinery for pathogen protein synthesis. |
| ** Viral peptides associate with MHC class I and are expressed on the cell surface. | | ** Viral peptides associate with MHC class I and are expressed on the cell surface. |
− | *** [[Lymphocytes - WikiBlood#Cytotoxic CD8+|CD8+ cytotoxic T-lymphocytes (CTL)]] recognise the antigen-MHC complex. | + | *** [[Lymphocytes#Cytotoxic CD8+|CD8+ cytotoxic T-lymphocytes (CTL)]] recognise the antigen-MHC complex. |
| * Cytotoxic T-cells secrete a pattern of cytokines similar to that of TH<sub>1</sub> cells. | | * Cytotoxic T-cells secrete a pattern of cytokines similar to that of TH<sub>1</sub> cells. |
| ** I.e. IFNγ but not IL-2. | | ** I.e. IFNγ but not IL-2. |
| *** The IFNγ shifts the balance of the immune response in favour of TH<sub>1</sub> cells. | | *** The IFNγ shifts the balance of the immune response in favour of TH<sub>1</sub> cells. |
− | **** There is therefore an increased level of [[Lymphocytes - WikiBlood#T cells|T-cell]] proliferation. | + | **** There is therefore an increased level of [[Lymphocytes#T cells|T-cell]] proliferation. |
| ***** The initiation of the immune response via CTL leads to the selective proliferation of CTL - enhances the main mechanism of killing of virally-infected cells. | | ***** The initiation of the immune response via CTL leads to the selective proliferation of CTL - enhances the main mechanism of killing of virally-infected cells. |
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| ==T-Cell Activation== | | ==T-Cell Activation== |
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− | * [[Lymphocytes - WikiBlood#T cells|T cells]] function only after recent activation by antigen. | + | * [[Lymphocytes#T cells|T cells]] function only after recent activation by antigen. |
| * CD4 binds [[MHC - WikiBlood#MHC II|MHC class II]]. | | * CD4 binds [[MHC - WikiBlood#MHC II|MHC class II]]. |
− | ** [[Lymphocytes - WikiBlood#Helper CD4+|CD4+ T-cells]] therefore recognise antigen only in association with [[MHC - WikiBlood#MHC II|MHC class II]] | + | ** [[Lymphocytes#Helper CD4+|CD4+ T-cells]] therefore recognise antigen only in association with [[MHC - WikiBlood#MHC II|MHC class II]] |
| * CD8 binds [[MHC - WikiBlood#MHC I|MHC class I]]. | | * CD8 binds [[MHC - WikiBlood#MHC I|MHC class I]]. |
− | ** [[Lymphocytes - WikiBlood#Cytotoxic CD8+|CD8+ T-cells]] recognise antigen only in association with [[MHC - WikiBlood#MHC I|MHC class I]]. | + | ** [[Lymphocytes#Cytotoxic CD8+|CD8+ T-cells]] recognise antigen only in association with [[MHC - WikiBlood#MHC I|MHC class I]]. |
− | * Activation of [[Lymphocytes - WikiBlood#T cells|T cells]] requires two distinct signals. | + | * Activation of [[Lymphocytes#T cells|T cells]] requires two distinct signals. |
| ** '''Signal 1''' | | ** '''Signal 1''' |
| *** The interaction of the TcR with the antigenic peptide/[[MHC - WikiBlood|MHC]] complex on the antigen presenting cell. | | *** The interaction of the TcR with the antigenic peptide/[[MHC - WikiBlood|MHC]] complex on the antigen presenting cell. |
| ** '''Signal 2''' | | ** '''Signal 2''' |
− | *** The interaction of CD28 on the [[Lymphocytes - WikiBlood#T cells|T cells]] with its ligand, CD80, on the antigen-presenting cell. | + | *** The interaction of CD28 on the [[Lymphocytes#T cells|T cells]] with its ligand, CD80, on the antigen-presenting cell. |
| **** APC expression of CD80 only occurs after: | | **** APC expression of CD80 only occurs after: |
| ***** The engagement of pattern recognition or Fc receptors. | | ***** The engagement of pattern recognition or Fc receptors. |
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| * '''No signal 1''' | | * '''No signal 1''' |
− | ** [[Lymphocytes - WikiBlood#T cells|T cells]] is not activated as there is no antigen. | + | ** [[Lymphocytes#T cells|T cells]] is not activated as there is no antigen. |
| * '''Both signal 1 and signal 2''' | | * '''Both signal 1 and signal 2''' |
− | ** [[Lymphocytes - WikiBlood#T cells|T cells]] is activated into clonal expansion. | + | ** [[Lymphocytes#T cells|T cells]] is activated into clonal expansion. |
| *** Produces cytokines or becomes cytotoxic. | | *** Produces cytokines or becomes cytotoxic. |
| ** This is the response to a dangerous antigen. | | ** This is the response to a dangerous antigen. |
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| ===Response to Activation=== | | ===Response to Activation=== |
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− | * The response of the [[Lymphocytes - WikiBlood#T cells|T cells]] to obtaining Signals 1 and 2 is: | + | * The response of the [[Lymphocytes#T cells|T cells]] to obtaining Signals 1 and 2 is: |
| ** To express the receptor for the cytokine interleukin-2 (IL-2). | | ** To express the receptor for the cytokine interleukin-2 (IL-2). |
− | ** In [[Lymphocytes - WikiBlood#Helper CD4+|CD4+ T-cells]] only, the secretion of IL-2. | + | ** In [[Lymphocytes#Helper CD4+|CD4+ T-cells]] only, the secretion of IL-2. |
| * The final trigger for clonal expansion is the engagement of IL-2R with IL-2. | | * The final trigger for clonal expansion is the engagement of IL-2R with IL-2. |
| ** The IL-2 can come from any activated CD4+ T-cell. | | ** The IL-2 can come from any activated CD4+ T-cell. |
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| [[B cell differentiation - WikiBlood|B Cell Development]] | | [[B cell differentiation - WikiBlood|B Cell Development]] |
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− | [[Lymphocytes - WikiBlood#Cytotoxic CD8+|Lymphocytes - WikiBlood]] | + | [[Lymphocytes#Cytotoxic CD8+|Lymphocytes]] |
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| [[Adaptive Immune System - WikiBlood#Structure and Function of MHC Class I|Major Histocompatability Complex (MHC) molecule]] | | [[Adaptive Immune System - WikiBlood#Structure and Function of MHC Class I|Major Histocompatability Complex (MHC) molecule]] |