Lymphoid_system_cells.pdf

The Immune System & Lymphoid cells Fevziye Figen Kaymaz M.D., Ph.D. Prof. of Histology & Embryology [email protected] 1 Learning goals • Explain cells of immune system 2 Function And Components Main function: to protect the organism from the effects of all nonself, substances as well as end...

The Immune System & Lymphoid cells Fevziye Figen Kaymaz M.D., Ph.D. Prof. of Histology & Embryology [email protected] 1 Learning goals • Explain cells of immune system 2 Function And Components Main function: to protect the organism from the effects of all nonself, substances as well as endogen abnormal structures Immune response: • Innate-Natural immunity : • (Acquired) Adaptive İmmunity 3 INNATE (Natural) IMMUNITY • The system of defenses termed innate immunity involves immediate, nonspecific actions, including physical barriers such as the skin and mucous membranes of the gastrointestinal, respiratory, and urogenital tracts that prevent infections or penetration of the host body. • Bacteria, fungi, and parasites that manage to penetrate these barriers are quickly removed by neutrophils and other leukocytes in the adjacent connective tissue. • Toll-like receptors (TLRs) on leukocytes allow the recognition and binding of surface components of such invaders. • Other leukocytes orchestrate the defenses at sites of penetration. • Natural killer (NK) cells destroy various unhealthy host cells, including those infected with virus or bacteria, as well as certain potentially tumorigenic cells. 4 Leukocytes and specific cells of the tissue barriers also produce a wide variety of antimicrobial chemicals that also form a major part of innate immunity including the following: • Hydrochloric acid (HCL) and organic acids in specific regions lower pH locally to either kill entering microorganisms directly or inhibit their growth • Defensins, short cationic polypeptides produced by neutrophils and various epithelial cells that kill bacteria by disrupting the cell walls. • Lysozyme, an enzyme made by neutrophils and cells of epithelial barriers, which hydrolyzes bacterial cell wall components, killing those cells • Complement, a system of proteins in blood plasma, mucus, and macrophages that react with bacterial surface components to aid removal of bacteria • Interferons, paracrine factors from leukocytes and virus-infected cells that signal NK cells to kill such cells and adjacent cells to resist viral infection. 5 ADAPTIVE (Acquired) IMMUNITY Adaptive immunity, acquired gradually by exposure to microorganisms, is more specific, slower to respond, and an evolutionarily more recent development than innate immunity. The adaptive immune response involves B and T lymphocytes, which become activated against specific invaders by being presented with specific molecules from those cells by APCs, which are usually derived from monocytes. Unlike innate immunity, adaptive immune responses are aimed at specific microbial invaders and involve production of memory lymphocytes so that a similar response can be mounted very rapidly if that invader ever appears again. 6 • Innate-Natural immunity :nonspecific no previous antigen exposure • • • • Epıthelia lining the cavities, and mucous membranes Macrophages, neutrophils Soluble factors, complement Natural killer cells • (Acquired) Adaptive İmmunity • • • • • • Specifity Diversity Memory Self- Nonself discrimination Tolerence Controlled response and duration Occur after antigen exposure 7 MEDICAL APPLICATION • Some pathogenic bacteria, such as Haemophilus influenzae and Streptococcus pneumoniae, avoid phagocytosis by granulocytes and macrophages of innate immunity by covering their cell walls with a “capsule” of polysaccharide. The capsule inhibits recognition and binding to the phagocytes’ receptors. Eventually such bacteria can be removed by antibody-based mechanisms, including phagocytosis after opsonization, but in the interim of several days the cells proliferate undisturbed and establish a more dangerous infection. Elderly or immunocompromised patients, with reduced adaptive immunity, are particularly susceptible to infections with such bacteria. 8 Components of adaptive immunity • Lymphoid organs and tıssues • Primary: Bone marrow. Thymus • Secondary: Lymph nodes. Spleen. Tonsilla- MALT • Cells • • • • T cell B cell APC Macrophages • Cytokines • Part of the blood vessels and lymphatics 9 CYTOKINES • CYTOKINES Within lymphoid organs and during inflammation at sites of infection or tissue injury, cells in the immune system communicate with each other primarily via cytokines to coordinate defensive measures. • Involved in both innate and adaptive immunity, cytokines are a diverse group of peptides and glycoproteins. They coordinate cell activities in the innate and adaptive immune responses. 10 Major responses induced in target cells by cytokines are the following: • Directed cell movements, or chemotaxis, toward and cell accumulation at sites of inflammation, for example, during diapedesis. Cytokines producing this effect are also called chemokines. • Increased mitotic activity in certain leukocytes, both locally and in the bone marrow. • Stimulation or suppression of lymphocyte activities in adaptive immunity. A group of cytokines with such effects were named interleukins because they were thought to be produced by and to target only leukocytes. • Stimulated phagocytosis or directed cell killing by innate immune cells. 11 12 Antigen and main immun response types in acquired immunity • Antigen: all nonself substances including bacteria, virus and molecules capable of inducing an immune response • Epıtope: Antigenic determinants: small moleculer domains on the antigen which can be selectivetely recognized by lymphocytes • Each indıvudual lymphocytes can recognize only one or two related epitope (genetically determined) • B cell after binding give rise to plasma cell, antibody immun globulin production Humoral immunity • T cell give rise to activated or effector T cell produce celluler or cell mediated immunity • Two type usually develop together against a given antigen 13 ANTIGENS & ANTIBODIES Antigen is a molecule that is recognized by cells of the adaptive immune system and typically elicits a response from these cells. • Antigens may consist of soluble molecules (such as proteins or polysaccharides) or molecules that are still components of intact cells (bacteria, protozoa, or tumor cells). • Immune cells recognize and react to small molecular domains of the antigen known as antigenic determinants or epitopes. • The immune response to antigens may be cellular (in which lymphocytes are primarily in charge of eliminating the antigen), humoral (in which antibodies are primarily responsible for the response), or both. 14 An antibody is a glycoprotein of the immunoglobulin family that interacts specifically with an antigenic determinant. • Antibodies are secreted by plasma cells that arise by terminal differentiation of clonally proliferating B lymphocytes whose receptors recognize and bind specific epitopes. • Antibodies either accumulate in the blood plasma and in the interstitial fluid of tissues or are transported across epithelia into the secretion of glands such as mucous, salivary, and mammary glands. • Other antibodies are membrane proteins on the surface of B lymphocytes or other leukocytes. • In all these situations each antibody combines with the epitope that it specifically recognizes. 15 Immunoglobulins of all antibody molecules have a common design, consisting of two identical light chains and two identical heavy chains bound by disulfide bonds • The isolated carboxyl-terminal portion of the heavy-chain molecules is called the constant Fc region. The Fc regions of some immunoglobulins are recognized by cell surface receptors on basophils and mast cells, localizing these antibodies to the surface of these cells. 16 • The first 110 amino acids near the amino-terminal ends of the light and heavy chains vary widely among different antibody molecules, and this region is called the variable region. The variable portions of one heavy and one light chain make up an antibody’s antigen-binding site. DNA sequences coding for these regions undergo recombination and rearrangement after B lymphocytes are activated against a specific antigen and the progeny of those cells all produce antibodies that specifically bind that antigen. • Each antibody has two antigen-binding sites, both for the same antigen. 17 Classes of Antibodies Immunoglobulins of humans has five major classes. The classes are called immunoglobulin G (IgG), IgA, IgM, IgE, and IgD, and key aspects for each include the following: • IgG is the most abundant class representing 75%-85% of the immunoglobulin in blood. Production increases during immune responses following infections, etc. Unlike the other classes of antibodies, IgG is highly soluble, stable (half-life > 3 weeks), and crosses the placental barrier into the fetal circulation. This confers passive immunity against certain infections until the newborn’s own adaptive immune system is acquired. 18 • IgA is present in almost all exocrine secretions as a dimeric form in which the heavy chains of two monomers are united by a polypeptide called the J chain. • IgA is produced by plasma cells in mucosae of the digestive, respiratory, and reproductive tracts. Another protein bound to this immunoglobulin, the secretory component, is released by the epithelial cells as IgA undergoes transcytosis. The resulting structure is relatively resistant to proteolysis and reacts with microorganisms in milk, saliva, tears, and mucus coating the mucosae in which it is made. 19 • IgM constitutes 5%-10% of blood immunoglobulin and usually exits in a pentameric form united by a J chain. IgM is mainly produced in an initial response to an antigen. IgM bound to antigen is the most effective antibody class in activating the complement system. 20 • IgE, usually a monomer, is much less abundant in the circulation and exists bound at its Fc region to receptors on the surface of mast cells and basophils. When this IgE encounters the antigen that elicited its production, the antigen-antibody complex triggers the liberation of several biologically active substances, such as histamine, heparin, and leukotrienes. This characterizes an allergic reaction, which is thus mediated by the binding of cell bound IgE with the antigens (allergens) that stimulated the IgE to be synthesized initially 21 • IgD, the least abundant immunoglobulin in plasma, is also the least understood class of antibody. Monomers of IgD are bound to the surface of B lymphocytes where they (along with IgM monomers) act as antigen receptors in triggering B-cell activation. 22 23 Actions of Antibodies antigen-binding sites of IgG and IgA antibodies are able to bind specifically and neutralize certain viral particles and bacterial toxins, agglutinate many bacterial cells, and precipitate most soluble antigens. 24 • the Fc portions of these and other antibodies also bind receptors for this sequence and thereby optimize three important actions of innate immunity: 25 1- Complement activation: Antigen-antibody complexes containing IgG or IgM bind polypeptides of the complement system, a group of around 20 plasma proteins produced mainly in the liver and activate them through a cascade of enzymatic reactions. After activation, specific complement components bind and rupture membranes of invading cells, clump antigenbearing bacteria or cells, and elicit arrival of relevant leukocytes. 2- Opsonization: This refers to the ability of receptors on macrophages, neutrophils, and eosinophils to recognize and bind the Fc portions of antibodies attached to surface antigens of microorganisms. Opsonization greatly increases the efficiency of phagocytosis by these leukocytes at the sites of infection. 3- NK cells activation: Antibodies bound to antigens on virus-infected cells of the body are recognized by the primitive lymphocytes called NK cells, which are then activated to kill the infected cell by releasing perforin and various granzymes. These two proteins together enter the infected cell via other receptors and cause apoptosis 26 ANTIGEN PRESENTATION Antigens recognized by lymphocytes are often bound to specialized integral membrane protein complexes on cell surfaces. These abundant antigen-presenting proteins are parts of the major histocompatibility complex (MHC), which includes the two key types called MHC class I and class II. These proteins were first recognized by their roles in the immune rejection of grafted tissue or organs. Proteins of both classes, which on human cells are often called human leukocyte antigens (HLAs), having very high degrees of allelic variation between different individuals. T lymphocytes are specialized to recognize both classes of MHC proteins and the antigens they present. If the MHCs on cells of a tissue graft are not similar to those that T lymphocytes encountered during their development, the grafted cells will induce a strong immune reaction by T cells of the recipient. To these lymphocytes, the unfamiliar MHC epitopes on the graft’s cells are recognized as markers of potentially tumorigenic, infected, or otherwise abnormal (“non-self”) cells that they must eliminate. 27 • Like all integral membrane protein complexes, MHC molecules are made in the rough ER and Golgi apparatus. Before leaving the ER, MHC class I proteins bind a wide variety of proteasome-derived peptide fragments representing the range of all proteins synthesized in that cell. • All nucleated cells produce and expose on their surfaces MHC class I molecules presenting such “self-antigens,” which T cells recognize as a signal to ignore those cells. • By this same mechanism, some virally infected cells or cells with proteins altered by gene mutation also have MHC class I proteins displaying peptides that T cells do not recognize as “self,” helping lead to the elimination of such cells. 28 • MHC class II proteins are synthesized and transported to the cell surface similarly but only in cells of the mononuclear phagocyte system and certain other cells under some conditions. Before joining the plasmalemma, the Golgi derived vesicles with the MHC class II complexes first fuse with endolysosomal vesicles containing antigens ingested by receptor-mediated endocytosis, pinocytosis, or phagocytosis This allows the class II proteins to bind fragments of whatever proteins the cells had ingested, including those from dead, infected, or abnormal cells and atypical proteins of all kinds. At the surface of these cells, the class II complexes display the peptides from these potentially pathogenic cells, signaling T lymphocytes and activating their responses against sources of these antigens. 29 MEDICAL APPLICATION • Tissue grafts and organ transplants are classified as autografts when the donor and the host are the same individual. Neither of these graft types is immunologically rejected. • Homografts (or allografts), which involve two related or unrelated individuals, consist of cells with MHC class I molecules and contain dendritic cells with MHC class II molecules, all presenting peptides that the host’s T cells recognize as “foreign,” leading to immune rejection of the graft. • Development of immunosuppressive drugs such as the cyclosporins, which inhibit the activation of cytotoxic T cells has allowed the more widespread use of allografts or even xenografts taken from an animal donor if allografts are in short supply. • Such immunosuppression can however lead to other immune-related problems, such as certain opportunistic infections or cancers 30 CELLS OF ADAPTIVE IMMUNITY • Lymphocytes and the monocyte-derived cells specialized for antigen presentation to lymphocytes are the major players in adaptive immune responses. 31 Antigen-Presenting Cells • Most specialized APCs are part of the mononuclear phagocyte system, including all types of macrophages and specialized dendritic cells in lymphoid organs. • Features common to all APCs are an active endocytotic system and expression of MHC class II molecules for presenting peptides of exogenous antigens. Besides dendritic cells (not to be confused with cells of nervous tissue) and all monocyte-derived cells, “professional” APCs also include thymic epithelial cells. • During inflammation transient expression of MHC class II is induced by interferon-γ in certain local cells that can be considered “nonprofessional” APCs, including fibroblasts and vascular endothelial cells. 32 Lymphocytes • Lymphocytes both regulate and carry out adaptive immunity. In adults stem cells for all lymphocytes are located in the red bone marrow, but cells of the major lymphoid lineages mature and become functional in two different central or primary lymphoid organs. • Cells destined to become B lymphocytes remain and differentiate further in the bone marrow. • Progenitors of T lymphocytes move via the circulation into the developing thymus. • After maturation in these primary structures, B and T cells circulate to the peripheral secondary lymphoid organs, which include the MALT, the lymph nodes, and the spleen • Lymphocytes do not stay long in the lymphoid organs; they continuously recirculate through the body in connective tissues, blood, and lymph. 33 • Lymphoid tissue is usually reticular connective tissue filled with large numbers of lymphocytes. • It can be either diffuse within areas of loose connective tissue or surrounded by capsules, forming secondary lymphoid organs. Because lymphocytes have prominent basophilic nuclei and very little cytoplasm, lymphoid tissue packed with such cells usually stains dark blue in hematoxylin and eosin (H&E) -stained sections. • In all secondary lymphoid tissue the lymphocytes are supported by a rich reticulin fiber network of type III collagen. The fibers are produced by fibroblastic reticular cells, which extend numerous processes along and around the fibers. • Besides lymphocytes and reticular cells, lymphoid tissue typically contains various APCs and plasma cells. 34 35 • Although most lymphocytes are morphologically indistinguishable in either the light or electron microscope, various surface proteins (“cluster of differentiation” or CD markers) allow them to be distinguished as B cells and subcategories of T cells by immunocytochemical methods. Key features of B and T lymphocytes also include the surface receptors involved in activating their different responses to antigens • Receptors of B cells are immunoglobulins that bind antigens directly; those on T cells react only with antigen on MHC molecules and this requires the additional cell surface proteins CD4 or CD8. 36 37 • Lymphocytes in the marrow and thymus of a newborn infant not yet exposed to antigens are immunocompetent but naive and unable to recognize antigens. After circulating to the various secondary lymphoid structures, lymphocytes are exposed to antigens on APCs and become activated, proliferating to produce a clone of lymphocytes all able to recognize that antigen. 38 T Lymphocytes • T cells are long-lived lymphocytes and constitute nearly 75% of the circulating lymphocytes. They recognize antigenic epitopes via surface protein complexes termed T-cell receptors (TCRs). Most TCRs include two glycoproteins called the α and β chains, each with variable regions produced similarly to those of immunoglobulins. Because TCRs only recognize antigenic peptides when presented as part of MHC molecules (interacting with both the MHC and the peptide it presents), T lymphocytes are said to be MHC restricted. Several types of T lymphocytes exist, with various functions. Important subpopulations of T cells include the following: 39 Helper T cells (Th cells) • Helper T cells (Th cells) are characterized by CD4, the coreceptor with the TCR for binding MHC class II molecules and the peptides they are presenting. Activated by such binding, helper T cells greatly assist immune responses by producing cytokines that promote differentiation of B cells into plasma cells, activate macrophages to become phagocytic, activate cytotoxic T lymphocytes (CTLs), and induce many parts of an inflammatory reaction. Some specifically activated helper T cells persist as long-lived memory helper T cells, which allow a more rapid response if the antigen appears again later. 40 CTLs • CTLs are CD8+. Their TCRs together with CD8 coreceptors bind specific antigens on foreign cells or virusinfected cells displayed by MHC class I molecules. In the presence of interleukin-2 (IL-2) from helper T cells, cytotoxic T cells that have recognized such antigens are activated and proliferate. Also called killer T cells, they attach to the cell sources of the antigens and remove them by releasing perforins and granzymes, which trigger apoptosis. This represents cellmediated immunity and its mechanism is largely similar to that of NK cells. Activation of cytotoxic T cells also results in a population of memory cytotoxic T cells. 41 42 Regulatory T cells • Regulatory T cells (Tregs or suppressor T cells) are CD4+CD25+ and serve to inhibit specific immune responses. These cells, also identified by the presence of the Foxp3 transcription factor, play crucial roles in allowing immune tolerance, maintaining unresponsiveness to selfantigens and suppressing excessive immune responses. These cells produce peripheral tolerance, which acts to supplement the central tolerance that develops in the thymus 43 γδ T lymphocytes • γδ T lymphocytes represent a smaller subpopulation whose TCRs contain γ (gamma) and δ (delta) chains instead of α and β chains. The γδ T cells migrate to the epidermis and mucosal epithelia, becoming largely intraepithelial, and do not recirculate to secondary lymphoid organs. They function in many ways like cells of innate immunity, in the front lines against invading microorganisms. 44 MEDICAL APPLICATION • The retrovirus that produces acquired immunodeficiency syndrome (AIDS) infects and rapidly kills helper T cells. Reduction of this key lymphocyte group cripples the patient’s immune system rendering them susceptible to opportunistic bacterial, fungal, protozoan, and other infections that usually dealt with easily in immunocompetent individuals. 45 B Lymphocytes • B lymphocytes the surface receptors for antigens are monomers of IgM or IgD, with each B cell covered by about 150,000 such B-cell receptors (BCRs). BCRs bind an antigen, which may be free in solution, on an exposed part of an infectious agent, or already bound to antibodies, and the surface complexes then undergo endocytosis. Degraded in endosomes, peptides from the antigens are presented on MHC class II molecules of the B cell. A helper T cell then binds this B cell and activates it further with a cytokine, inducing recombination in the immunoglobulin genes and stimulating several cycles of cell proliferation. 46 • In all secondary lymphoid tissues B lymphocytes interact with scattered follicular dendritic cells (FDCs), which have long filamentous processes. Unlike other dendritic cells, FDCs are mesenchymal in origin and their function does not involve MHC class II molecules. Surfaces of these cells are covered with antibody-antigen complexes bound to receptors for complement proteins and for immunoglobulin Fc regions, causing B cells to attach, become activated, and aggregate as a small primary lymphoid nodule (or follicle). With the help of adjacent T cells, these B cells now form a much larger and more prominent secondary lymphoid nodule. 47 Lymphatic Nodules or Follicles • Primary follicle • Secondary follicle • Mantle or Cap • Germinal Centre Dark and pale Pole. • • • • • • Lymphoblasts (B) Proliferating lymphocytes ,Centrocytes T helper FDC Macrophages (Folliculer or “tingible body” ) İmmunological Memory 48 49 • Secondary nodules are characterized by a lightly stained germinal center filled with large lymphoblasts (or centroblasts) undergoing immunoglobulin gene recombination, rapid proliferation, and quality control. Growth of activated B cells in germinal centers is exuberate and very rapid, causing naive, nonproliferating B cells to be pushed aside and produce the more darkly stained peripheral mantle 50 • After 2-3 weeks of proliferation, most cells of the germinal center and mantle are dispersed and the structure of the secondary lymphoid nodule is gradually lost. • Most of these new, specific B lymphocytes differentiate into plasma cells secreting antibodies that will bind the same epitope recognized by the activated B cell. Because the antibodies specified by B cells circulate in lymph and blood throughout the body, B cells are said to provide humoral immunity. 51 • As with activated T cells, some of the newly formed B cells remain as long-lived memory B cells. Formation of longlived memory lymphocytes is a key feature of adaptive immunity, which allows a very rapid response upon subsequent exposure to the same antigen. 52 Types of lymphoid Tissues • Diffuse lymphoid tissue • Nodular lymphoid tissue Lymphatic nodules or follicles • Loose lymphoid tissue 53 Diffuse Lymphoid Tissue • Rich in Tcells • İDC as antigen presenting cells • Deep cortex of the Lymph nodes • Medullary cords of the lymph nodes • White pulp of the spleen • HEV 54 Loose lymphoid tissue • Medullary Sinuses of the lymph nodes • Rich in phagocytic cells 55 • Primary (central) lymphoid organs are responsible for the development and maturation of lymphocytes into mature, immunocompetent cells. • Secondary (peripheral) lymphoid organs are responsible for the proper environment in which immunocompetent cells can react with each other, as well as with antigens and other cells, to mount an immunological challenge against invading antigens or pathogens 56