Antigen processing and presentation involves specialized antigen presenting cells internalizing antigens, degrading them into peptides, and displaying the peptides bound to MHC molecules on their surface. There are two pathways - the exogenous pathway where external antigens are degraded and presented on MHC class II to activate TH cells, and the endogenous pathway where internal antigens are degraded and presented on MHC class I to activate TC cells and target infected or cancerous cells for destruction. The MHC molecules play a key role in antigen recognition by T cells in both pathways.
Antigen processing and presentation involves specialized antigen presenting cells internalizing antigens, degrading them into peptides, and displaying the peptides bound to MHC molecules on their surface. There are two pathways - the exogenous pathway where external antigens are degraded and presented on MHC class II to activate TH cells, and the endogenous pathway where internal antigens are degraded and presented on MHC class I to activate TC cells and target infected or cancerous cells for destruction. The MHC molecules play a key role in antigen recognition by T cells in both pathways.
Antigen processing and presentation involves specialized antigen presenting cells internalizing antigens, degrading them into peptides, and displaying the peptides bound to MHC molecules on their surface. There are two pathways - the exogenous pathway where external antigens are degraded and presented on MHC class II to activate TH cells, and the endogenous pathway where internal antigens are degraded and presented on MHC class I to activate TC cells and target infected or cancerous cells for destruction. The MHC molecules play a key role in antigen recognition by T cells in both pathways.
Antigen processing and presentation involves specialized antigen presenting cells internalizing antigens, degrading them into peptides, and displaying the peptides bound to MHC molecules on their surface. There are two pathways - the exogenous pathway where external antigens are degraded and presented on MHC class II to activate TH cells, and the endogenous pathway where internal antigens are degraded and presented on MHC class I to activate TC cells and target infected or cancerous cells for destruction. The MHC molecules play a key role in antigen recognition by T cells in both pathways.
M.Sc. 1ST YEAR BIOTECHNOLOGY MANIPAL UNIVERSITY JAIPUR Antigen Presenting Cells Antigen-presenting cells (APCs) are specialized cells, which include macrophages, B lymphocytes, and dendritic cells, are distinguished by two properties: (1)they express class II MHC molecules on their membranes, and (2)they are able to deliver a co-stimulatory signal that is necessary for TH-cell activation. Antigen-presenting cells first internalize antigen, either by phagocytosis or by endocytosis, and then display a part of that antigen on their membrane bound to a class II MHC molecule. The TH cell recognizes and interacts with the antigen–class II MHC molecule complex on the membrane of the antigen-presenting cell leading to the initiation of a costimulatory signal by the antigen-presenting cell, leading to activation of the TH cell. Major Histocompatibility Complex (MHC)
The MHC loci encode two major classes of
membrane-bound glycoproteins: class I and class II MHC molecules. They function as antigen-recognition molecules. TH cells recognize antigen combined with class II molecules, whereas TC cells generally recognize antigen combined with class I molecules. MHC molecule can bind to a spectrum of antigenic peptides derived from the intracellular degradation of antigen molecules. These variable regions form a cleft within which the antigenic peptide sits and is presented to T lymphocytes. Antigen Processing & Presentation Foreign protein antigen are degraded into small antigenic peptides that form complexes with class I or class II MHC molecules. This conversion of proteins into MHC-associated peptide fragments is called antigen processing and presentation. Whether a particular antigen will be processed and presented together with class I MHC or class II MHC molecules appears to be determined by the route that the antigen takes to enter a cell. Exogenous pathway
Exogenous antigen is produced outside of the
host cell and enters the cell by endocytosis or phagocytosis. Antigen presenting cells (macrophages, dendritic cells, and B cells) degrade ingested exogenous antigen into peptide fragments within the endocytic processing pathway. Class II MHC molecules are expressed within the endocytic processing pathway and that peptides produced by degradation of antigen in this pathway bind to the cleft within the class II MHC molecules. The MHC molecules bearing the peptide are then exported to the cell surface to be recognized by TH cells. Processing of Exogenous Antigen Endogenous pathway
Endogenous antigen is produced within the
host cells. Viral proteins synthesized within virus-infected host cells. Unique proteins synthesized by cancerous cells. Endogenous antigens are degraded into peptide fragments that bind to class I MHC molecules within the endoplasmic reticulum. The peptide–class I MHC complex is then transported to the cell membrane. Since all nucleated cells express class I MHC molecules, all cells producing endogenous antigen use this route to process the antigen.
These cytotoxic T cells attack and kill cells displaying the
antigen–MHC class I complexes for which their receptors are specific. Processing of Endogenous Antigen Overview of the Immune Thank you
Antonio Daniele Pinna, Giorgio Ercolani (Eds.) - Abdominal Solid Organ Transplantation - Immunology, Indications, Techniques, and Early Complications-Springer International Publishing (2015)