Innate and Adaptive Immunity Quiz
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Questions and Answers

What is the primary characteristic of innate defenses?

  • They primarily depend on B and T lymphocytes.
  • They involve cells and molecules present at all times. (correct)
  • They are activated after days of infection.
  • They can distinguish between different types of pathogens.
  • Which statement best describes the role of mechanical and chemical defenses in immune response?

  • They are part of adaptive immunity.
  • They require activation for full effectiveness.
  • They serve as the first line of defense against pathogens. (correct)
  • They are less effective than adaptive immunity.
  • What distinguishes innate immunity from adaptive immunity?

  • Innate immunity can adapt to various pathogens.
  • Adaptive immunity acts within minutes of infection.
  • Adaptive immunity provides immediate response.
  • Innate immunity is present continuously. (correct)
  • What happens if pathogens are not cleared by the innate immune system?

    <p>They are handled by the adaptive immune system.</p> Signup and view all the answers

    How quickly can innate defenses be activated following an infection?

    <p>Within hours to minutes after infection.</p> Signup and view all the answers

    Which layer of immune defense provides a rapid deployment force against pathogens?

    <p>Innate immunity</p> Signup and view all the answers

    What is a limitation of innate immunity?

    <p>It has a limited ability to distinguish between pathogens.</p> Signup and view all the answers

    What is the time frame for the full activation of adaptive immunity?

    <p>Days after the initial exposure.</p> Signup and view all the answers

    What role do chemical defenses play in the immune system?

    <p>They prevent infection by acting as a first line of defense.</p> Signup and view all the answers

    What is the main function of lymph nodes in the immune system?

    <p>To filter lymphatic fluid and initiate adaptive immune responses.</p> Signup and view all the answers

    Which cell types are primarily involved in the adaptive immune response?

    <p>T-cells and B-cells.</p> Signup and view all the answers

    The lymphatic system is responsible for returning fluid to which part of the body?

    <p>The circulatory system.</p> Signup and view all the answers

    Which component is crucial for bridging the innate and adaptive immune responses?

    <p>The complement system.</p> Signup and view all the answers

    What is the primary role of antigen-laden dendritic cells in the immune response?

    <p>They present antigens to T cells.</p> Signup and view all the answers

    What is the relationship between innate immunity and adaptive immunity?

    <p>Innate immunity provides immediate defense while adaptive immunity provides long-term protection.</p> Signup and view all the answers

    Where do T cells exit the lymph node?

    <p>Through efferent lymphatic vessels.</p> Signup and view all the answers

    After interacting productively with T cells, what do B cells do?

    <p>They move into follicles and differentiate into plasma cells.</p> Signup and view all the answers

    What is primarily filtered by lymph nodes as part of their immune function?

    <p>Pathogens and foreign particles from lymphatic fluid.</p> Signup and view all the answers

    Which part of the immune system is mainly targeted by the adaptive immune response?

    <p>Specific antigens presented by pathogens.</p> Signup and view all the answers

    How long does a typical circulation cycle for T and B cells take?

    <p>12-24 hours</p> Signup and view all the answers

    What is the primary function of the thoracic duct?

    <p>To return lymph to the circulation.</p> Signup and view all the answers

    What is the role of C1q in the complement system?

    <p>It organizes the C1 complex.</p> Signup and view all the answers

    How does C3b function in the immune response?

    <p>It labels pathogens for phagocytosis.</p> Signup and view all the answers

    Which component of the C1 complex is responsible for cleaving molecules of C3?

    <p>C1s</p> Signup and view all the answers

    What structural feature is characteristic of C1q?

    <p>It possesses long collagen-like tails.</p> Signup and view all the answers

    Which statement accurately describes C1q's composition?

    <p>It is made up of six identical globular heads.</p> Signup and view all the answers

    What is implied by the presence of the C1 complex?

    <p>It is the initial trigger for the classical complement pathway.</p> Signup and view all the answers

    What role do opsonins play in the immune system?

    <p>They facilitate the recognition of pathogens by phagocytes.</p> Signup and view all the answers

    Which of the following best describes the action of C3 in the complement cascade?

    <p>It enhances the opsonization of pathogens.</p> Signup and view all the answers

    What is the primary function of C3b in the complement system?

    <p>To serve as an opsonin</p> Signup and view all the answers

    What does the cleavage of C4 by activated C1s produce?

    <p>C4a and C4b</p> Signup and view all the answers

    Which of the following statements is true regarding C4a?

    <p>C4a acts as an anaphylatoxin</p> Signup and view all the answers

    Which molecule acts as C5 convertase in the complement pathway?

    <p>C4b.2b.3b</p> Signup and view all the answers

    What role does C5b play in the complement system?

    <p>It recruits additional complement proteins</p> Signup and view all the answers

    Which pairs of molecules are involved in the initial recognition of antigens in the classical pathway?

    <p>IgM and C1</p> Signup and view all the answers

    How does C1s become activated in the complement cascade?

    <p>Through the presence of antigens</p> Signup and view all the answers

    Which of the following components is released as a byproduct during the cleavage of C5?

    <p>C5a</p> Signup and view all the answers

    What is the ultimate outcome of the complement cascade?

    <p>Formation of the membrane attack complex</p> Signup and view all the answers

    What is the initial processing step in the classical complement pathway?

    <p>C1s cleaving C4</p> Signup and view all the answers

    What is the primary function of the membrane attack complex (MAC) composed of complement proteins C5b-C9?

    <p>To create pores in the membranes of pathogens</p> Signup and view all the answers

    How does the mannose-binding lectin (MBL) bind to carbohydrates?

    <p>Only to mannose residues with correct spacing</p> Signup and view all the answers

    Which receptor enhances the detection of pathogens by phagocytes when bound with antibodies?

    <p>Fc receptor</p> Signup and view all the answers

    What similarity do the MBL pathway and the classical pathway share?

    <p>They both form a complex with serine proteases</p> Signup and view all the answers

    What type of residues does MBL specifically bind to?

    <p>Carbohydrates with specific spacing like mannose and fucose</p> Signup and view all the answers

    What enhances the ability of phagocytes to recognize and engulf pathogens?

    <p>Cooperation between Fc and complement receptors</p> Signup and view all the answers

    How does the spacing of mannose and fucose residues affect MBL binding?

    <p>Only correct spacing of residues allows MBL to bind effectively</p> Signup and view all the answers

    What component of the complement system forms the membrane attack complex?

    <p>C5b fragment</p> Signup and view all the answers

    Study Notes

    Innate Immunity

    • Vertebrate immune defenses have three layers
      • Mechanical/chemical defenses: Epithelia and skin, low pH gastric environment, antibacterial enzymes
      • Innate immunity: Phagocytic cells (neutrophils, dendritic cells, macrophages), natural killer (NK) cells, complement proteins, interleukins (IL-1, IL-6)
        • Rapid activation (minutes to hours)
        • Limited ability to distinguish between pathogens
      • Adaptive immunity: B and T lymphocytes
        • Requires days for full activation
        • Enhanced by innate immune response products
        • Antibodies facilitate innate immunity

    Lymphatic System

    • Network of conduits carrying lymph
    • Lymph nodes: Filter lymph, mature white blood cells (500-600 in humans)
    • Lymph vessels: Convey lymph
    • Thoracic duct: Discharges lymph into blood
    • Bone marrow: B cell development, T cell precursors
    • Thymus: T cell maturation
    • Spleen: Lymphocyte maturation, filters lymph

    Adaptive Immune Response in Lymph Nodes

    • Lymph nodes filter fluid returning to major collecting ducts.
    • Antigens are carried in two forms:
      • Soluble antigens
      • Antigen-laden dendritic cells
    • Soluble antigens bind to B cells.
    • Antigen-laden dendritic cells activate T cells.
    • Interactions between T and B cells lead to B cell differentiation.
    • Plasma cells produce antibodies.
    • Lymphocytes recirculate between lymph and blood (12-24 hours).
    • Activated dendritic cells migrate to the infection site via blood.
    • Dendritic cells carry microbial peptides to lymph nodes.
    • Activated dendritic cells activate T cells with appropriate receptors.

    Complement System

    • Heat-sensitive plasma component enhancing opsonization & killing of bacteria.
    • Many plasma proteins interacting to opsonize pathogens.
    • Induces inflammatory responses to fight infection.
    • Three pathways (classical, lectin, alternative) activate complement proteins via proteolytic cleavage.
    • Classical pathway: Activated by antigen-antibody complexes, C1 (C1q, C1r, C1s) binds to the antibody constant region or directly to pathogen surface. This causes a conformational change, activating C1s (serine protease)
    • Lectin pathway: Activated by mannose-binding lectin (MBL) binding to pathogen surfaces.
    • Alternative pathway: Activated by pathogen surfaces. Factor B binds to C3b, Factor D cleaves factor B into Bb and Ba, forming C3 convertase (C3bBb). Complement proteins act as opsonins (to tag) and inflammatory mediators (C3a, C4a, C5a)

    Complement Activation (Classical Pathway)

    • C1s cleaves C4 to C4a+ C4b; C4b binds to pathogen surface.
    • C1s cleaves C2 to C2a + C2b; C4b binds C2b = C3 convertase (C4b2b).
    • C3 convertase cleaves C3 to C3a+ C3b; C3b is an opsonin that binds to the microbial surface or to the convertase.
    • C3b binds to C4b2b = C5 convertase.
    • C5 convertase cleaves C5 to C5a +C5b. C5b initiates the formation of the membrane attack complex (MAC).
    • C5b recruits C6, C7, C8-C9 proteins into membrane-bound pores to cause cytolysis.
    • Complement proteins enhance phagocytosis.

    Antibody Structure and Digestion

    • Immunoglobulins are globular proteins with heavy and light chains.
    • Five classes (IgA, IgD, IgE, IgG, IgM).
    • Light chains are 2 types (κ and λ).
    • Heavy chains define isotype.
    • Constant regions vary by isotype.
    • Papain digestion cleaves IgG into two F(ab) fragments and one Fc fragment.
    • Pepsin digestion cleaves IgG into one F(ab')2 fragment and one Fc fragment degraded
    • F(ab) is monovalent (one antigen binding site)
    • F(ab')2 is bivalent (two antigen binding sites).
    • Immunoglobulin isotypes vary in structure of Fc and other elements.

    Transcytosis of IgA and IgG

    • IgA & IgG transported across epithelia
      • IgA binds to the polymeric IgA receptor (pIgR) and is endocytosed.
      • pIgR transports IgA across epithelium releasing the secretory IgA piece and the antibody.

    Immunological Memory (Primary and Secondary Responses)

    • Primary response: Mostly IgM, some IgG.
    • Secondary response: Faster and greater response, mostly IgG, some IgM, IgA, IgE.
    • Memory to antigen A during second immunization
    • Secondary response is specific to antigen A.
    • Antibodies in secondary response bind with tighter affinity to antigen.

    VDJ Recombination

    • This mechanism randomly assembles genes coding for specific immune proteins.
    • RAG1 and RAG2 enzymes are involved to recognize and induce DNA cleavage at recombination signal sequences (RSS).
    • V, D, and J segments combine to create a unique variable domain in immunoglobulin.

    Antibody Diversity

    • V, D, and J segments are rearranged randomly in the heavy chain variable region.
    • Similar rearrangements occur in the light chain variable region (V and J segments).

    Antibody Structure

    • Antibodies consist of heavy and light chains linked by disulfide bonds.
    • V(Variable) segments account for variability in antigen binding.
    • C(Constant) segments define isotypes and effector functions.

    Immunoglobulin Isotypes

    • Five isotypes (IgM, IgD, IgG, IgA, IgE).
    • IgM is usually produced first in response to a pathogen.

    Classes of Immunoglobulins

    • IgM, IgD : Monomers
    • IgA: Dimer
    • IgG: Monomer
    • IgE: Monomer

    Structure of T-cell Receptor (TCR)

    • TCR is a heterodimer (α and β chains).
    • Associates with CD3 complex for signal transduction.
    • Interacts with co-receptors (CD4 or CD8) for MHC binding.

    Signal Transduction from TCR and BCR

    • Src kinases (Lck, Fyn, Lyn) phosphorylate ITAMs.
    • ITAMs recruit non-Src kinases (ZAP-70, Syk)
    • Activated kinases activate various downstream signalling molecules.

    Class I and Class II MHC Proteins

    • Class I MHC proteins are expressed on most nucleated cells (not RBCs).
    • MHC class I associated with ß2-microglobulin, presents peptides from intracellular proteins (e.g., virally-infected cells).
    • Class II MHC are expressed primarily by professional APCs (dendritic cells, macrophages, B cells).
    • MHC class II present peptides from extracellular proteins.
    • An individual has many different MHC alleles providing variability in peptide presentation.

    Cytokines in T-cell Activation

    • IL-2, IL-4 and IL-7 influence CD4+ T-cell differentiation
    • IL-12 & IFNγ influence CD4+ T-cells into TH1 cells.

    Cytotoxic T Cells (CTLs)

    • CTLs recognize viral peptides presented by class I MHC.
    • Release perforins and granzymes to induce target cell death.

    Activation of B Cells

    • Three signals required for B-cell activation.
      • Antigen recognition by BCR.
      • CD40L on TH cell binds to CD40 receptor.
      • Cytokines stimulate B cell responses.

    Positive Selection of T Cells

    • Thymocytes that bind to self-MHC survive.
    • Thymocytes binding to foreign antigens die or are rejected via apoptosis.

    Negative Selection of T Cells

    • Thymocytes recognizing self-antigens are eliminated or undergo receptor editing.
      • Prevents autoimmune reactions.

    MHC Proteins and Viral Infections

    • Viruses can evade CTL destruction by suppressing MHC class I expression, making the infected cells a target for NK cells.
    • NK cells have activating receptors that target infected or cancer cells.
    • Inhibitory receptors recognise MHC-I molecules on healthy cells.

    Toll-like Receptors (TLRs)

    • TLRs recognize pathogen-associated molecular patterns (PAMPs).
    • Initiate innate immune system activation.

    Antigen Cross Presentation

    • Some antigen presenting cells (APCs) can present extracellular antigens on MHC class I to CD8 T cells.

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