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30 General, Organic, and Biochemistry, 7e Bettelheim, Brown, and March © 2003 Thomson Learning, Inc. All rights reserved 30-1 30 Chapter 30 Immunochemistry © 2003 Thomson Learning, Inc. All rights reserved 30-2 30 The Immune System • Figure 30.1 An overview of the immune system © 2003 Thomson Learning, Inc. All rights reserved 30-3 30 Innate Immunity • • • • the first line of defense has two forms: external and internal is nonspecific and without memory after a pathogen penetrates a tissue, innate immunity creates physiological barriers, such as high O2 pressure • when natural killer (NK) cells encounter cancerous cells, viral infected cells, or other suspicious cells, they attach themselves to these cells • there is a proliferation of macrophages, which engulf and digest bacteria and reduce inflammation • the capillaries dilate to allow greater flow of blood to the site of an injury © 2003 Thomson Learning, Inc. All rights reserved 30-4 30 Adaptive Immunity • also called acquired immunity • key features are specificity and memory • uses antibodies specifically designed for each type of invader • the invader may be bacteria, viruses, molds, or pollen grains • in a second encounter with the same invader, the response is more rapid, more vigorous, and more prolonged • the system is flexible; it is capable of making millions of potential defenders © 2003 Thomson Learning, Inc. All rights reserved 30-5 30 Components • antigen: a foreign substance that invades the body • two types of white blood cells (lymphocytes) fight against invaders: T cells and B cells • T cells kill invaders by contact • B cells synthesize antibodies, which are soluble immunoglobins • the basic molecules of the immune system belong to the immunoglobin superfamily • The immunoglobin superfamily • all are glycoproteins • the polypeptide chains of each have a constant region and a variable region © 2003 Thomson Learning, Inc. All rights reserved 30-6 30 Immunoglobin Superfamily • the constant region has the same amino acid sequence in each of the same class of molecules • the variable region is antigen specific • The three representatives of the Ig superfamily: • antibodies, which are soluble immunoglobins secreted by the plasma cells • T cell receptors (TcR), which recognize and bind antigens presented to them • major histocompability complex (MCH), which interacts with an antigen and brings a characteristic portion of it to the surface of the cell; such a surface presentation them marks the diseased cell for destruction © 2003 Thomson Learning, Inc. All rights reserved 30-7 30 Speed of Immune Response • the process of making the right immunoglobin is relatively slow, often taking weeks and months • the immune system is complex in that it involves molecular signals and an interplay between various cells • its major elements are: 1. cells of the immune system 2. antigens and their perception by the immune system 3. antibodies designed to immobilize antigens 4. receptors on cells that recognize antigens 5. cytokines that control these interactions © 2003 Thomson Learning, Inc. All rights reserved 30-8 30 Organs and Cells • exchange of compounds among three body fluids © 2003 Thomson Learning, Inc. All rights reserved 30-9 30 Lymphoid Organs • Lymphoid organs • the lymphatic capillary vessels drain the fluids that bath the cells of the body • the fluid in these vessels is called lymph • lymphatic vessels circulate throughout the body and enter lymphatic organs such as the thymus, spleen, tonsils, and lymph nodes • lymphocytes are found primarily in the lymphoid organs; lymphocytes may be specific for a given antigen or nonspecific • T cells are lymphocytes that originate in bone marrow but mature in the thymus gland © 2003 Thomson Learning, Inc. All rights reserved 30-10 30 Lymphoid Organs • B cells are lymphocytes that originate and mature in the bone marrow • both T and B cells are found mostly in the lymph, but small numbers are also found in the blood • their entry into the blood is aided by signaling molecules called cytokines © 2003 Thomson Learning, Inc. All rights reserved 30-11 30 The Immune System Infection Interferon N O synthetas e N onsp ecific Macrop hages engulf bacteria or virus an d digest them Antigens (d iges ted ) are p res ented on the su rface of macrophages T cells B cells Sp ecific Killer T cells Memory cells Plasma cells © 2003 Thomson Learning, Inc. All rights reserved 30-12 30 Internal Innate Immunity • Cells of the internal innate immunity • the two important cells are macrophages and natural killer cells • Macrophages • they are nonspecific; they attack virtually anything that is not recognized as part of the body • they engulf nonself, destroy it, and display a small portion of it on their surface • Natural killer (NK) cells • target abnormal cells • once in contact, they release proteins called performins that perforate target cell membranes © 2003 Thomson Learning, Inc. All rights reserved creating pores 30-13 30 Cells of Adaptive Immunity • The two types of cells are T and B cells • T cells interact with the antigen presented by the macrophage and produce other T cells that are now highly specific to the antigen • when these T cells differentiate, they become killer T cells • killer T cells act through perforin • other T cells become memory cells • B cells are produced by plasma cells • most plasma cells reside in lymph nodes © 2003 Thomson Learning, Inc. All rights reserved 30-14 30 Antigens and MHC • Antigen: any molecule, usually foreign, capable of eliciting synthesis of a specific antibody in vertebrates • they are also called immunogens • three features characterize an antigen 1. foreignness 2. a molecular weight greater than 6000 3. sufficient complexity to elicit a response • the smallest unit of an antigen capable of binding an antibody is called the epitope • to elicit a response, the antigen or epitope must be brought to the surface of the infected cell © 2003 Thomson Learning, Inc. All rights reserved 30-15 30 MHC © 2003 Thomson Learning, Inc. All rights reserved 30-16 30 Immunoglobins • Classes of immunoglobins Class Molecular Weight IgA IgD IgE IgG IgM 200,00 - 700,00 160,000 190,000 150,000 950,000 © 2003 Thomson Learning, Inc. All rights reserved Carbohydrate Seru m Con tent Concen tration (%) (mg/100 mL) 7 - 12 <1 10 - 12 2-3 10 - 12 90 - 420 1 - 40 0.01 - 0.1 600 - 1800 50 - 90 30-17 30 Immunoglobins © 2003 Thomson Learning, Inc. All rights reserved 30-18 30 Immunoglobins © 2003 Thomson Learning, Inc. All rights reserved 30-19 30 Immunoglobins © 2003 Thomson Learning, Inc. All rights reserved 30-20 30 B Cells and Antibodies • antibody binding to the epitope of an antigen © 2003 Thomson Learning, Inc. All rights reserved 30-21 30 Divserification of Igs © 2003 Thomson Learning, Inc. All rights reserved 30-22 30 Monoclonal Antibodies • when an antigen is injected into an organism, it may be 1 to 2 weeks before an antibody appears in the serum • the antigen may have many epitopes, and the antisera contains a mixture of immunoglobins with varying epitope specificities • even antibodies to a single epitope usually have a variety of specificities • monoclonal antibodies, in contrast, are the product of cells cloned from a single B cell and have a single specificity © 2003 Thomson Learning, Inc. All rights reserved 30-23 30 T Cells and Their Receptors • T Cell Receptors • each different T cell carries on its surface a unique T cell receptor (TcR) that is specific for one antigen only • a TcR is a glycoprotein made of two different subunits cross-linked by disulfide bonds • like immunoglobins, TcRs also have a constant (C) and variable (V) regions • TcRs can only interact when the epitope of an antigen is presented by a MHC © 2003 Thomson Learning, Inc. All rights reserved 30-24 30 TcR Complex © 2003 Thomson Learning, Inc. All rights reserved 30-25 30 TcR Complex • TcR alone, however, is not sufficient for antigen binding • also needed are proteins called cluster determinants (CD) that act as coreceptors and/or signal transducers • CD3 is a signal transducer • upon antigen binding, CD3 becomes phosphorylated which sets up a signaling cascade inside the cell • CD4 and CD8 act as adhesion molecules as well as signal transducers • a unique feature of CD4 is that it binds strongly to a glycoprotein on the surface of HIV • through this binding to CD4, an HIV can enter and infect T cells and cause AIDS © 2003 Thomson Learning, Inc. All rights reserved 30-26 30 Cytokines • Cytokines: glycoproteins that are produced by one cell and alters the function of another cell • cytokines have no antigen specificity • they are short lived and are not stored in cells • they are released in bursts in response to all manner of insult or injury • they travel and bind to specific cytokine receptors on the surface of macrophage and B and T cells, and induce cell proliferation • one set of cytokines are the interleukins (ILs) • macrophages secrete IL-1 upon bacterial infection © 2003 Thomson Learning, Inc. All rights reserved 30-27 30 Classes of Cytokines • Cytokines are classified by the secondary structure of their polypeptide chains 1. four a-helical segments • an example is IL-2, which activates other B and T cells and macrophages 2. only b-pleated sheets in 2° structure • an example is tumor necrosis factor (TNF) 3. both a-helical and b-pleated sheets segments • an example is epidermal growth factor (EGF) 4. a subgroup called chemotactic cytokines (chemokines) • they attract leukocytes to the site of infection or inflammation © 2003 Thomson Learning, Inc. All rights reserved 30-28 30 Action of Cytokines • when a tissue in injured, leukocytes are rushed to the inflamed area • cytokines help them migrate out of blood vessels to the site of injury • cytokines are also major players in chronic inflammations autoimmune diseases asthma and other forms of allergic inflammation transplant rejection © 2003 Thomson Learning, Inc. All rights reserved 30-29 30 How to Recognize Self • One of the major problems facing body defenses is how to recognize a foreign body as “not self” and avoid attacking “self” • Selection of T and B cells • T cells mature in the thymus gland • during maturation, those T cells that fail to interact with MHC and thus cannot respond to foreign antigen are eliminated through a selection process • T cells that express receptors TcR that are prone to interact with normal self antigens are also eliminated through a selection process © 2003 Thomson Learning, Inc. All rights reserved 30-30 30 How to Recognize Self • Selection of T and B cells (cont’d) • the maturation of B cells in the bone marrow depends on their engagement with their receptors, BcR, with antigen • those B cells that are prone to interact with self antigens are eliminated before they leave the bone marrow • many signaling pathways control the proliferation of B cells © 2003 Thomson Learning, Inc. All rights reserved 30-31 30 How to Recognize Self • Discrimination of the cells of the innate system • natural killer cells and macrophages have no specific targets and no memory of what epitopes signal danger • still, they must discriminate between normal and abnormal cells • innate immunity cells have activating receptors and inhibitory receptors on their surfaces • an inhibitory receptor recognizes the epitome of a normal cell, binds to it, and prevents activation of killer cells or macrophages • when a macrophage encounters a foreign antigen, the antigen binds to the activating receptor; this binding prompts the macrophage to destroy the antigen © 2003 Thomson Learning, Inc. All rights reserved 30-32 30 How to Recognize Self • Autoimmune diseases • in spite of the safe guards to prevent acting against “self”, some parts of the immune system may go awry • autoimmune diseases include the skin diseases psoriasis and eczema myasthenia gravis rheumatoid arthritis multiple sclerosis insulin-dependent diabetes allergies Crohn’s disease © 2003 Thomson Learning, Inc. All rights reserved 30-33 30 How to Recognize Self • Autoimmune diseases (cont’d) • the major drugs for treating autoimmune diseases are the glucocorticiods, the most important of which is cortisol • the glucocorticoids regulate the synthesis of cytokines either by interacting directly with their genes or indirectly through transcription factors • macrolid drugs, such as cyclosporine A and rapamycin, bind to receptors in the cytosol and, through secondary messengers, inhibit the entrance of nuclear factors into the nucleus • the absence of nuclear factors prevents transcription of cytokines © 2003 Thomson Learning, Inc. All rights reserved 30-34 30 Immunochemistry End Chapter 30 © 2003 Thomson Learning, Inc. All rights reserved 30-35