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The immune system and the oral cavity 2nd part Adaptive or acquired immunity Done by Dr. Zubaida Najat Adaptive Immune System – Introduction  Adaptive: responds to specific foreign substances  Innate & adaptive mechanisms work together Types of Acquired Immunity Figure 21.11 Types of Acquired Immunity 1- Passive acquired immunity includes a- Naturally passive acquired immunity antibodies are pass through placenta of fetus   b- Artificially passive acquired immunity:The injection of alredy prepared antibodies such as gamma globulin 2- Active immunity a- Natural active acquired immunity Following clinical or subclinical infections  b-Artificial active acquired immunity:- Following vaccination with live or killed infectious agents or their products [[[[[ Adaptive Immune System: Cells   Lymphocytes  T-cells  B-cells Antigen Presenting Cells (APCs)        Acquired immunity is triggered in vertebrates when a pathogen evades the innate immune system and (1) generates a threshold level of antigen and (2) generates "stranger" or "danger" signals activating dendritic cells The major functions of the acquired immune system include: Recognition of specific "non-self" antigens in the presence of "self", during the process of antigen presentation. Generation of responses that are tailored to maximally eliminate specific pathogens or pathogen-infected cells systemic action . Development of immunological memory, in which pathogens are "remembered" through memory B cells and memory T cells. Antibody Targets & Functions  Immune complex formation = antigen-antibody binding.  All the following events are initiated by antigen-antibody binding. Complement fixation: Neutralization: Agglutination: Precipitation: Inflammation & phagocytosis prompted by debris      Adaptive, Humoral Immunity  Antigen – “any substance when introduced into the body stimulates the production of an antibody” – Bacteria, fungus, parasite – Viral particles – Other foreign material  Pathogen – an Antigen which causes disease Adaptive, Humoral Immunity  Complete antigens (proteins, nucleic acids, lipids, polysaccharides):  Immunogenicity: the ability to stimulate specific lymphocytes & specific antibodies  Reactivity: the ability to react with activated lymphocytes & antibodies  Hapten (an incomplete antigen): a smaller molecule that is not immunogenic until attached to proteins Adaptive, Humoral Immunity  Antigenic determinants: sites on an antigenic molecule that are immunogenic   Epitope Major Histocompatibility Complex (MHC): cell surface glycoproteins associated with self recognition Humoral Immunity  Active humoral immunity:  B-cells encounter & respond to antigen to produce an antibody  Passive humoral immunity:  Introduced “non-native” antibody Antibodies      Antibody – “a Y-shaped protein, found on the surface of B-Cells or free in the blood, that neutralize antigen by binding specifically to it” Also known as an Immunoglobulin Constant (C) region defines antibody class determines chemical & cellular interactions determines how class functions to eliminate antigens Humoral Mediated Immunity Antibodies   Immunoglobulins & gamma globulins Structure  variable  hypervariable  constant Figure 21.13a Antibody Classes  Antibody Classes: IgM, IgG, IgA, IgD, IgE (Ig = immunoglobulin) Antibody Classes  IgM: occurs as a monomer & a pentamer  Occurs  The on the B-cell surface (Monomer). Ig of early primary plasma cell response, circulating antibody; a potent agglutinator. Complement binding (Pentamer). Antibody Classes  IgE: the Ig associated with allergies.  Stem binds to mast cells & basophils.  Receptor binding results in histamine release & inflammation.  Found mostly in mucosa of respiratory & GI tract (Monomer). Antibody Classes  IgG: the most abundant circulating Ig. The dominant circulating Ig of the primary & the secondary response. Crosses the placenta. Complement binding (Monomer).  IgA: the Ig of secretions. Helps prevent antigen penetration of membranes (Dimer).  IgD: the Ig of B-cell activation. Found on B-cell surface (Monomer). Adaptive Immune System: Cells  Immunocompetence: as T- or B-cells mature they become immunocompetent, they display receptors on their cell membrane for a specific antigen.  All of the receptors on one cell are identical; immunity depends upon genetic coding for appropriate receptors. Immunocompetent B or T cells Key: Red bone marrow = Site of development of immunocompetence as B or T cells; primary lymphoid organs = Site of antigen challenge & final differentiation to activated B & T cells Immature lymphocytes Circulation in blood = Site of lymphocyte origin 1 1 Lymphocytes destined to become T 1 Thymus Bone marrow cells migrate to the thymus & develop immunocompetence there. B cells develop immunocompetence in red bone marrow. 2 Immunocompetent, but still naive, lymphocyte migrates via blood 2 2 After leaving the thymus or bone marrow as naive immunocompetent cells, lymphocytes “seed” the lymph nodes, spleen, & other lymphoid tissues where the antigen challenge occurs. Lymph nodes, spleen, & other lymphoid tissues 3 Mature (antigen-activated) 3 Activated immunocompetent B & T cells recirculate in blood & lymph 3 immunocompetent lymphocytes circulate continuously in the bloodstream & lymph & throughout the lymphoid organs of the body. Figure 21.8 Adaptive Immune System: Cells Antigen Presenting Cells (APCs) APCs ingest foreign material, then present antigenic fragments on their cell surface where they are recognized by T-cells APCs: Macrophages & B lymphocytes Interactions between APCs & lymphocytes & lymphocyte-lymphocyte interactions are critical to immune response Adaptive, Humoral response  Humoral response (clonal selection) Figure 21.14 Cellular Immunity Tcell CD4& CD8 Adaptive Immune System: Cells Lymphocytes: initially uncommitted T-cells: are sorted in the Thymus Positive selection: recognize MHC survive Negative selection: react against to self-antigens on MHC killed 2% of initial T-cell precursors T-cells manage the immune response Cell Mediated Immune Response  T-cell activation: involves recognition of PM surface antigens only  Antigen is combined with MHC & displayed on PM  T-cell receptors: bind to the MHC & are stimulated by the associated antigen  The addition of a co-stimulator (cytokines, interleukins, etc) prompts the T-cell to form a clone Helper T Cells (TH) Figure 21.17a Professional APCs + CD4 Th1-Cells Cell Mediated: MHC  MHC occurs as two classes  MHC I on virtually all tissue cells  MHC II only on PM some immune system cells Cell Mediated: MHC display properties  MHC I on virtually all tissue cells  Display only proteins produced inside the cell  Endogenous antigens = foreign proteins produced by the cell (viral / cancer)  Stimulate the CD8* cell population  form cytotoxic T-cells (Killer T, TC)  *formerly T8 cells Cell Mediated: MHC display properties Figure 21.16b  MHC II found only on PM of B-cells, some T-cells & APCs  Display proteins derived from a phagocytized target  Exogenous antigen: foreign protein from outside the cell – presented to PM surface  Stimulates the CD4* cell population  form Helper T-cells (TH) Cell Mediated: T-cell roles  Helper T-cells (TH) stimulate B-cells & other T-cells to proliferate Figure 21.18 Cell Mediated: T-cell roles  Activated TH cells interact with Bcells displaying antigen & produce cytokines that prompt the B-cell to mature & form antibody Cell Mediated: T-cell roles  TH cells also produce cytokines that promote TC cells  TH cells recruit other WBCs & amplify innate defenses (inflammatory) Subpopulations of TH cells specialize in specific sets of activations  Cell Mediated: T-cell roles   Cytotoxic T-cells (TC, Killer T): directly attack & kill cells with specific antigen Activated TC cells are co-stimulated by TH cells Cell Mediated: T-cell roles  TC mechanism (Cytotoxic T-cells, Killer T)      TC binds to cell & releases perforin & granzymes In the presence of Ca2+ perforin forms pores in target cell PM Granzymes enter through pores & degrade cellular contents TC then detaches & moves on Macrophages clean up Cell Mediated: T-cell roles  Other T-cells  *Regulatory T-cells (TReg): release inhibitory cytokines that suppress B-cell & T-cell activity   Help to prevent autoimmune events *formerly Suppressor T (TS)  Gamma Delta T-cells (Tgd): live in the intestine. Function in surveillance & are triggered much like NK cells Cellular Mediated Immunity Summary of the Primary Immune Response Figure 21.19