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| + | #REDIRECT[[:Category:Lymphocytes]] |
| − | |<gallery perrow="1">
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| − | Image:LH_Lymphocyte_Histology.jpg|<div style="text-align: center;"><p>'''Lymphocyte'''</p><sup>©RVC 2008</sup></div>
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| − | Image:LH_Lymphocytes_Histology.jpg|<div style="text-align: center;"><p>'''Lymphocytes'''</p><sup>©RVC 2008</sup></div>
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| − | </gallery>
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| − | |}
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| − | <p>
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| − | Lymphocytes account for around a third of all circulating [[Leukocytes|leukocytes]] and are formed in a variety of lymphoid tissues. They are functionally divided into [[#T cells|T cells]], [[#B cells|B cells]] and [[#Natural Killer (NK) Cells|NK (Natural Killer) cells]]. Lymphocytes vary in size (6-30µm) and are classified as small, medium or large. Large cells are either activated lymphocytes or NK cells. The vast majority of circulating lymphocytes are small and of a similar size to erythrocytes. Histologically they are round with a densely staining nucleus and a thin, often indistinct, rim of cytoplasm. While NK cells can be distinguished by their large granules and kidney shaped nucleus, B and T cells appear the same histologically.</p>
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| − | <p>Lymphocytes, along with associated supporting cells, form the immune system and recognise antigens, produce antibodies and destroy pathogens.</p>
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| − | ==Development==
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| − | <p>Both T and B lymphocytes develop from a common stem cell ([[Haematopoiesis#Colony Forming Units|CFU-L's]]) and for a general overview of this process see [[Leukopoiesis#Lymphopoiesis|here]].</p>
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| − | <p> Follow these links for a more detailed explanation on [[T cell differentiation - WikiBlood|T cell development]] and [[B cell differentiation - WikiBlood|B cell development]].</p>
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| − | ==T cells==
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| − | [[Image:TCR2.jpg|thumb|right|150px|T-cell receptor binds antigen fragments presented by MHC on the cell surface - B. Catchpole, RVC 2008]]
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| − | [[Image:T Cell diagram 2.jpg|thumb|right|150px|T Cell - Copyright Prof Dirk Werling DrMedVet PhD MRCVS]]
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| − | ''Also called T lymphocytes''
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| − | <p>So named as they differentiate in the [[Thymus - Anatomy & Physiology|thymus]]. They are long lived and are involved in cell mediated immunity. They represent 60-80% of the circulating lymphocytes and all express the markers CD2, CD3 and CD7 as well as having T cell receptors (TCR). Each T cell has 30,000 TCRs each of which is identical and recognises antigens and MHC II.</p><p>Functionally they are divided into three subsets that are distinguished by presence or absence of CD4 or CD8 markers. CD4 and CD8 cells have α/β antigen receptors while the γδ cells have the γ/δ antigens receptors.</p>
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| − | * T-cell receptors are the antigen-specific receptors for T-lymphocytes
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| − | * T-cell receptors are a combination of either αβ chains or γδ chains
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| − | ** One T-cell will express either αβ OR γδ TCR
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| − | * The antigen-binding site of the TCR is produced by a combination of the V domains of either 1α and 1β chain or 1γ and 1δchain
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| − | ** Like antibody, the specificity of TCR is determined by the '''amino acid composition of the variable domains'''
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| − | * TCR are '''always''' linked to the cell membrane
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| − | * Like antibody, TCR consist of a distal domain and a membrane proximal constant domain
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| − | ** Structurally, they look like a single arm of an antibody molecule
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| − | ===Helper CD4+===
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| − | <p>These T cells express the marker CD4 and are categorised into two groups, Th1 and Th2, which are distinguished by the cytokines they produce. T helper cells recognise antigens bound to MHC II complex.
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| − | *Th1 cells produce Il-2, IFN-γ and TNF-α
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| − | *Th2 cells produce Il-4, Il-5, Il-10 and Il-13
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| − | Th1 cells interact with CD8<sup>+</sup>, NK and dendritic cells and Th2 cells interact with B cells. Th1 cells are involved with the control of intracellular pathogens and Th2 cells extracellular pathogens. Il-2 produced by Th1 cells stimulates further proliferation of CD4<sup>+</sup> cells.</p>
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| − | <p>Th0 populations are CD4<sup>+</sup> cells that have yet to differentiate into Th1 or Th2 cells and they secrete Il-2, IL-4, Il-5, IFN-γ. In the presence of Il-4 they develop into Th2 cells while in the presence of Il-12 they develop into Th1 cells. In the abscence of Il-12 Th1 cells will change into Th2 cells.</p>
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| − | <p>Th1 cells have two populations. One that secretes IFN-γ and is short lived, and the other that doesn’t secrete IFN-γ and is long lived. The IFN-γ<sup>-</sup> cells are termed memory T cells (This relationship is not the case for Il-4<sup>+</sup> and Il-4<sup>-</sup> Th2 cells).</p>
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| − | <p>For more information on T helper cells click [[T cell differentiation - WikiBlood#TH1 Cells|here]]
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| − | ===Cytotoxic CD8<sup>+</sup>===
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| − | <p>These T cells express the marker CD8 and once fully mature seek and destroy target cells (infected or cancer forming cells). When the cytotoxic T cell recognises the MHC I complex on the target cell (MHC I binds to TCR) the T cell kills that cell e.g. viral peptides associate with MHC I and the CD8<sup>+</sup> T cell recognises this and binds to the cell. Only two pathways are used by cytotoxic T cells to kill cells:
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| − | *One pathway uses the CD95 (death receptor) which triggers apoptosis in the target cell (usually other T cells)
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| − | *The other pathway uses perforins and granzymes which form pores in the target cell membrane causing cell lysis
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| − | **Perforins are structurally related to complement factor C9
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| − | **Granzymes are proteolytic enzymes that target cell nucleases and cause apoptosis
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| − | In both cases direct contact is required between the T cell and target cell, and cell killing can take several minutes.</p><p> Cytotoxic T cells secrete a pattern of cytokines similar to that of TH1 cells i.e. IFN-γ but not IL-2. IFN-γ shifts the balance of the immune response in favour of TH1 cells giving an increased level of T cell proliferation. The initiation of the immune response via cytotoxic T cells leads to the selective proliferation of cytotoxic T cells enhancing the main mechanism of killing infected cells.</p>
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| − | ===γδ cells===
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| − | <p>''Information on these cells is varied.''</p>
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| − | <p>They do not express CD4 or CD8 and have γδ antigen receptors rather than α/β like other T cells. They develop in the [[Thymus - Anatomy & Physiology|thymus]] and migrate to epithelial tissues where they remain. The number present in an individual varies greatly but is generally greatest in immature ruminants and pigs.</p>
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| − | <p>The cells can be divided into two subsets:
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| − | *One with restricted antigen binding, that act as first line defence against invading organisms and recognises antigens bound to MHC I complex
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| − | *The other subset doesn’t require the MHC complex and this subset has a further two subsets
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| − | ** One producing cytokines and chemokines (Th1 and Th2)
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| − | **The other having cytotoxic effects.</p>
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| − | [[Image:LH B cells Peyers Patch Histology.jpg|right|thumb|150px|<p>'''B Cells in Lymph node'''</p><sup>©RVC 2008</sup>]]
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| − | ==B Cells==
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| − | ''Also called B lymphocytes''
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| − | <p>So named as they were initially found in the [[Bursa of Fabricius - Anatomy & Physiology|Bursa of Fabricius]]. They produce antibodies (Ig’s) and are associated with humoral immunity. They represent 20-30% of circulating lymphocytes.
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| − | B cells have B cell receptors (BCR), or antigen binding sites. This is IgM when the B cell is immature, changing to IgD when the cell is mature. B cells also express MHC II, CD9, CD,19, CD20 and CD24.</p>
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| − | <p>Under antigenic stimulation they differentiate into [[B cell differentiation - WikiBlood#Plasma cells|plasma cells]] and [[B cell differentiation - WikiBlood#Memory cells|memory cells]].</p>
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| − | B-cells also act as Antigen-Presenting Cells (APCs) by presenting digested fragments to T-cells on [[MHC - WikiBlood#MHC II|MHC II]].
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| − | For more on B cell differentiation, see [[B cell differentiation - WikiBlood|here]].
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| − | ==Natural Killer (NK) cells==
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| − | [[Image:NK healthy.jpg|thumb|right|150px|Healthy cells present MHC to NK cells to suppress their activation - B. Catchpole, RVC 2008]]
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| − | [[Image:NK infected.jpg|thumb|right|150px|Infected cells lack MHC, which means they cannot switch off the NK activation signal - B. Catchpole, RVC 2008]]
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| − | [[Image:NK activated.jpg|thumb|right|150px|Natural Killer cells release enzymes to kill cells with inadequate MHC presentation - B. Catchpole, RVC 2008]]
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| − | [[Image:NK kill.jpg|thumb|right|150px|Infected cells are destroyed before replication - B. Catchpole, RVC 2008]]
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| − | NK cells can be classified as lymphocytes because they are capable of recognising antigen, however they are more often associated with the [[Innate Immune System - WikiBlood|innate]] immune response. They target cells by monitoring [[MHC - WikiBlood|MHC]] production, which is expressed by healthy cells to present antigen to T-cells. Low MHC levels can be used as a marker for a cell whose machinery is compromised by a replicating virus. When MHC levels drop, it acts as a danger signal to the NK cells, which then release enzymes to kill the infected cells.
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| − | NK cells do not develop in the thymus and represent 5-10% of the circulating lymphocytes. They recognise and kill transformed cells by releasing perforins and granzymes which create channels in the target cell membrane causing lysis. They express the markers CD16, CD56 and CD94.
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| − | Natural Killer cells also play a role in [[Adaptive Immune System - WikiBlood#Adaptive Immunity to Viruses|'''Antibody-Dependent Cell-mediated Cytotoxicity''']]
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| − | ===NK Receptors===
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| − | * Some viruses down-regulate MHC expression of the infected cell
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| − | ** This is used as a protection against the host immune system
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| − | *** Lack of MHC inhibits normal T-cell activity
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| − | * NK cells can counteract the down-regulation tactic
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| − | ** They are mainly associated with activity against virus-infected cells and tumour cells, which can also have lowered MHC expression
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| − | * The receptors on NK cells '''do not''' act like antigen-specific receptors
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| − | ** Although they trigger functional activity of the cell, they do not stimulate proliferation
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| − | *** There is no clonal expansion of NK cells
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| − | * NK cells work through two different types of receptors
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| − | ** '''Activating receptors, R1'''
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| − | *** Recognise pathogen-associated glycolipids or Fc receptors
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| − | **** E.g. CD16 recognises Ig that is bound to pathogen antigens
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| − | ** '''Suppressing receptors, R2'''
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| − | *** Recognise target cell MHC molecules
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| − | * When an NK cell interacts with a target cell it will be activated via R1
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| − | ** If the target cell expresses MHC this will be seen by R2
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| − | *** R2 suppresses the activities of the NK cells
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| − | **** Therefore, NK cells do not affect normal cells
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| − | ** If the target cell does not express MHC, the suppressing receptors are not engaged
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| − | *** Cell activity is not suppressed
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| − | **** The engagement of R1 therefore causes activation of the NK cells
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| − | When NK cells are activated, they:
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| − | *Secrete a range of [[Cytokines - WikiBlood|cytokines]], including:
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| − | ** '''Tumour necrosis factor alpha'''; (TNFα)
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| − | *** A potent stimulator of acute inflammation
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| − | ***Can cause target cell killing directly and also via stimulated macrophages
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| − | **'''Interferon gamma'''; (IFNγ)
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| − | *** Stimulates macrophages
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| − | *** Active against the target cells
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| − | **** Stimulates target cell expression of MHC
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| − | **** Makes target cells susceptible to normal T-cell killing.
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| − | *Initiate killing of the target cell
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| − | ==Lymphocyte Surveillance==
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| − | <p>About two thirds of lymphocytes (all immunocompetent) are circulating in the blood and lymph systems. Most of these are [[Lymphocytes#T cell|T cell]] and long lived. In the lymphatic system they survey tissues. The other third do not circulate and are either short lived or immature, or can be specific cells destined for certain tissues i.e. cells that line connective tissue under the epithelium of respiratory, intestinal and urogential systems.</p>
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| − | <p>[[Lymph Nodes - Anatomy & Physiology#High endothelial venules|High Endothelial Venules (HEV)]] are used for lymphocytes to access the [[Lymph Nodes - Anatomy & Physiology|lymph nodes]] from the bloodstream. Once inside the [[Lymph Nodes - Anatomy & Physiology|lymph node]], the naive lymphocytes search for antigen. If there is no antigen present, the naive lymphocytes leave via the efferent lymphatic vessel and return back to the bloodstream. Each lymphocyte can search several [[Secondary Lymphoid Tissue - Anatomy & Physiology|secondary lymphoid organs]] each day. This process is called '''surveillance'''.</P>
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| − | <p>If a naive lymphocyte recognises an antigen then it differentiates into its adult (mature) form. [[T cell differentiation - WikiBlood#Dendritic Cells|Interdigitating dendritic cells]] present antigen to [[Lymphocytes#T cells|T cells]] and [[B cell differentiation - WikiBlood#Follicular Dendritic Cells|follicular dendritic cells]] present antigen to [[Lymphocytes#B cells|B cells]].</p>
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| − | <p>[[Lymphocytes#B cells|B cells]] proliferate into [[B cell differentiation - WikiBlood#Plasma cells|plasma cells]] in germinal centres, producing antibody.</p>
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| − | <p>[[Lymphocytes#T cells|T cells]] leave the lymph node in '''attack mode''' to locate the infectious organism. The surface molecule L-selectin (which allows the naive lymphocyte to enter the lymph node via an [[Lymph Nodes - Anatomy & Physiology#High endothelial venules|HEV]]) is replaced by the adhesion molecule VLA-4. At the site of inflammation, the VLA-4 receptor recognises VCAM-1 on endothelial cells and the [[Lymphocytes#T cell|T cell]] enters the site of disease. [[Lymphocytes#Helper CD4+|CD4+ T cells]] search for infected macrophages and [[Lymphocytes#Cytotoxic CD8+|CD8+ T cells]] look for virus infected cells creating an immune response. After the infection has been defeated, memory cells develop which express L-selectin (rather than VLA-4) and continue to search the body in surveillance mode in case the host is re-infected with the disease producing organism.
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| − | ==Links==
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| − | '''WikiVet'''
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| − | *[[Chronic Inflammation - Pathology#Lymphocytic Inflammation|Lymphocytic Inflammation]]
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| − | | |
| − | *[[Changes in Inflammatory Cells Circulating in Blood - Pathology#Lymphocytosis|Lymphocytosis]]/[[Changes in Inflammatory Cells Circulating in Blood - Pathology#Lymphopenia|Lymphopenia]]
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| − | *[[T cell differentiation - WikiBlood|T Cell Differentiation and Function]]
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| − | *[[B cell differentiation - WikiBlood|B Cell Differentiation and Function]]
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| − | *[[Adaptive Immune System - WikiBlood#T Cell Dependent and Independent Responses|T Cell Independent and T Cell Dependent Responses]]
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| − | *[[Adaptive Immune System - WikiBlood#Immunoglobulin Class Switching|Immunoglobulin Class Switching]]
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| − | *[[Adaptive Immune System - WikiBlood#Structure and Function of MHC Class I|Major Histocompatability Complex (MHC) molecule]]
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| − | '''Websites'''
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| − | *http://www.cellsalive.com/antibody.htm
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| − | ----
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| − | <center><b><sup>Blood cells: [[Erythrocytes|Erythrocytes]] |
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| − | [[Basophils|Basophils]], [[Eosinophils|Eosinophils]], [[Lymphocytes|Lymphocytes]], [[Macrophages|Macrophages]], [[Mast Cells|Mast cells]], [[Monocytes|Monocytes]] & [[Neutrophils|Neutrophils]] | [[Thrombocytes|Thrombocytes]] & [[Thrombopoiesis#Megakaryocyte|Megakaryocytes]]</sup></b></center>
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