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Antigen-presenting cell

An antigen-presenting cell (APC) or accessory cell is a cell that displays antigen complexed with major histocompatibility complexes (MHCs) on their surfaces; this process is known as antigen presentation. T cells may recognize these complexes using their T cell receptors (TCRs). APCs process antigens and present them to T-cells. An antigen-presenting cell (APC) or accessory cell is a cell that displays antigen complexed with major histocompatibility complexes (MHCs) on their surfaces; this process is known as antigen presentation. T cells may recognize these complexes using their T cell receptors (TCRs). APCs process antigens and present them to T-cells. Almost all cell types can present antigens in some way. They are found in a variety of tissue types. Professional antigen-presenting cells, including macrophages, B cells and dendritic cells, present foreign antigens to helper T cells, while other cell types can present antigens originating inside the cell to cytotoxic T cells. In addition to the MHC family of proteins, antigen presentation relies on other specialized signaling molecules on the surfaces of both APCs and T cells. Antigen-presenting cells are vital for effective adaptive immune response, as the functioning of both cytotoxic and helper T cells is dependent on APCs. Antigen presentation allows for specificity of adaptive immunity and can contribute to immune responses against both intracellular and extracellular pathogens. It is also involved in defense against tumors. Some cancer therapies involve the creation of artificial APCs to prime the adaptive immune system to target malignant cells. Antigen-presenting cells fall into two categories: professional and non-professional. Those that express MHC class II molecules along with co-stimulatory molecules and pattern recognition receptors are often called professional antigen-presenting cells. The non-professional APCs express MHC class I molecules. T cells must be activated before they can divide and perform their function. This is achieved by interacting with a professional APC which presents an antigen recognized by their T cell receptor. The APC involved in activating T cells is usually a dendritic cell. T cells cannot recognize and therefore cannot respond to, 'free' or soluble antigens. They can only recognize and respond to antigen that has been processed and presented by cells via carrier molecules like MHC molecules. Helper T cells can recognize exogenous antigen presented on MHC class II; cytotoxic T cells can recognize endogenous antigen presented on MHC class I. Most cells in the body can present antigen to CD8+ cytotoxic T cells via MHC class I; however, the term 'antigen-presenting cell' is often used specifically to describe professional APCs. Such cells express MHC class I and MHC class II molecules and can stimulate CD4+ helper T cells as well as cytotoxic T cells. APCs can also present foreign and self lipids to T cells and NK cells by using the CD1 family of proteins, which are structurally similar to the MHC class I family. Professional APCs specialize in presenting antigen to T cells. They are very efficient at internalizing antigens, either by phagocytosis e.g macrophages or by receptor-mediated endocytosis (B cells), processing the antigen into peptide fragments and then displaying those peptides, bound to a class II MHC molecule, on their membrane. The T cell recognizes and interacts with the antigen-class II MHC molecule complex on the membrane of the antigen-presenting cell. An additional co-stimulatory signal is then produced by the antigen-presenting cell, leading to activation of the T cell. The expression of co-stimulatory molecules and MHC class II are defining features of professional APCs. All professional APCs also express MHC class I molecules as well. The main types of professional antigen-presenting cells are dendritic cells, macrophages and B cells. Dendritic cells have the broadest range of antigen presentation and are necessary for activation of naive T cells. DCs present antigen to both helper and cytotoxic T cells. They can also perform cross-presentation, a process by which they present exogenous antigen on MHC class I molecules to cytotoxic T cells. Cross-presentation allows for the activation of these T cells. Dendritic cells also play a role in peripheral tolerance, which contributes to prevention of auto-immune disease.

[ "Cytotoxic T cell", "T cell", "Gp100 antigen", "T follicular helper cell differentiation", "Peripheral tolerance induction", "Naive B cell", "Cytotoxic T cell differentiation", "CLEC7A", "Interleukin 3", "Mixed Leukocyte Reactions", "Phosphatidylserine binding protein", "APC activation", "T-Cell Antigen Receptors", "B-Cell Activation Antigen", "Streptamer", "B-1 cell", "Mouse Dendritic Cell", "Killer cell lectin like receptor G1", "T cell extravasation", "Autologous Cellular Immunotherapy", "Polyclonal B cell response", "Immunological synapse formation", "Non-peptidic antigen", "Follicular B helper T cells", "CCL5", "Veiled cell", "TCIRG1", "Lymph Node Paracortex", "Lymphocyte costimulation", "Cross-presentation", "Memory T cell proliferation", "Autologous dendritic cells", "T-cell tolerance induction", "Atrial Premature Complexes", "Janus kinase 3", "FDC-SP", "Supramolecular activation cluster", "INDUCIBLE T-CELL COSTIMULATOR LIGAND", "CD11c Antigen", "Follicular dendritic cell tumor", "Artificial antigen presenting cells", "CD278", "Transitional B-Cells", "Interdigitating Dendritic Cell", "NK-92", "ctla4 ligand", "Inducible T-cell costimulator", "Follicular dendritic cells", "CD1", "Impaired T cell activation", "Atacicept", "Lymphocyte Cooperation", "Follicular dendritic cell sarcoma", "CLIP peptide", "Dendritic cell sarcoma", "B7 Molecules", "Bromohydrin pyrophosphate", "OKM5 Antigen", "Cells t-helper", "Cross-priming", "CD49b", "Myeloid Dendritic Cell", "B7 Costimulatory Molecules", "Immunological Synapses", "Interdigitating Cells", "ZAP70", "Antigen Targeting", "Spleen accessory", "Increased T cell activation", "Follicular dendritic cell tumour", "Gamma-delta T cell activation", "Follicular dendritic cell differentiation", "Lymph node medulla", "Lymph Node Subcapsular Sinus", "Influenza Matrix Peptide", "exogenous antigen" ]
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