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Questions and Answers
What is the primary characteristic of innate defenses?
What is the primary characteristic of innate defenses?
Which statement best describes the role of mechanical and chemical defenses in immune response?
Which statement best describes the role of mechanical and chemical defenses in immune response?
What distinguishes innate immunity from adaptive immunity?
What distinguishes innate immunity from adaptive immunity?
What happens if pathogens are not cleared by the innate immune system?
What happens if pathogens are not cleared by the innate immune system?
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How quickly can innate defenses be activated following an infection?
How quickly can innate defenses be activated following an infection?
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Which layer of immune defense provides a rapid deployment force against pathogens?
Which layer of immune defense provides a rapid deployment force against pathogens?
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What is a limitation of innate immunity?
What is a limitation of innate immunity?
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What is the time frame for the full activation of adaptive immunity?
What is the time frame for the full activation of adaptive immunity?
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What role do chemical defenses play in the immune system?
What role do chemical defenses play in the immune system?
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What is the main function of lymph nodes in the immune system?
What is the main function of lymph nodes in the immune system?
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Which cell types are primarily involved in the adaptive immune response?
Which cell types are primarily involved in the adaptive immune response?
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The lymphatic system is responsible for returning fluid to which part of the body?
The lymphatic system is responsible for returning fluid to which part of the body?
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Which component is crucial for bridging the innate and adaptive immune responses?
Which component is crucial for bridging the innate and adaptive immune responses?
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What is the primary role of antigen-laden dendritic cells in the immune response?
What is the primary role of antigen-laden dendritic cells in the immune response?
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What is the relationship between innate immunity and adaptive immunity?
What is the relationship between innate immunity and adaptive immunity?
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Where do T cells exit the lymph node?
Where do T cells exit the lymph node?
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After interacting productively with T cells, what do B cells do?
After interacting productively with T cells, what do B cells do?
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What is primarily filtered by lymph nodes as part of their immune function?
What is primarily filtered by lymph nodes as part of their immune function?
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Which part of the immune system is mainly targeted by the adaptive immune response?
Which part of the immune system is mainly targeted by the adaptive immune response?
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How long does a typical circulation cycle for T and B cells take?
How long does a typical circulation cycle for T and B cells take?
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What is the primary function of the thoracic duct?
What is the primary function of the thoracic duct?
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What is the role of C1q in the complement system?
What is the role of C1q in the complement system?
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How does C3b function in the immune response?
How does C3b function in the immune response?
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Which component of the C1 complex is responsible for cleaving molecules of C3?
Which component of the C1 complex is responsible for cleaving molecules of C3?
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What structural feature is characteristic of C1q?
What structural feature is characteristic of C1q?
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Which statement accurately describes C1q's composition?
Which statement accurately describes C1q's composition?
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What is implied by the presence of the C1 complex?
What is implied by the presence of the C1 complex?
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What role do opsonins play in the immune system?
What role do opsonins play in the immune system?
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Which of the following best describes the action of C3 in the complement cascade?
Which of the following best describes the action of C3 in the complement cascade?
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What is the primary function of C3b in the complement system?
What is the primary function of C3b in the complement system?
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What does the cleavage of C4 by activated C1s produce?
What does the cleavage of C4 by activated C1s produce?
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Which of the following statements is true regarding C4a?
Which of the following statements is true regarding C4a?
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Which molecule acts as C5 convertase in the complement pathway?
Which molecule acts as C5 convertase in the complement pathway?
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What role does C5b play in the complement system?
What role does C5b play in the complement system?
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Which pairs of molecules are involved in the initial recognition of antigens in the classical pathway?
Which pairs of molecules are involved in the initial recognition of antigens in the classical pathway?
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How does C1s become activated in the complement cascade?
How does C1s become activated in the complement cascade?
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Which of the following components is released as a byproduct during the cleavage of C5?
Which of the following components is released as a byproduct during the cleavage of C5?
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What is the ultimate outcome of the complement cascade?
What is the ultimate outcome of the complement cascade?
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What is the initial processing step in the classical complement pathway?
What is the initial processing step in the classical complement pathway?
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What is the primary function of the membrane attack complex (MAC) composed of complement proteins C5b-C9?
What is the primary function of the membrane attack complex (MAC) composed of complement proteins C5b-C9?
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How does the mannose-binding lectin (MBL) bind to carbohydrates?
How does the mannose-binding lectin (MBL) bind to carbohydrates?
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Which receptor enhances the detection of pathogens by phagocytes when bound with antibodies?
Which receptor enhances the detection of pathogens by phagocytes when bound with antibodies?
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What similarity do the MBL pathway and the classical pathway share?
What similarity do the MBL pathway and the classical pathway share?
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What type of residues does MBL specifically bind to?
What type of residues does MBL specifically bind to?
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What enhances the ability of phagocytes to recognize and engulf pathogens?
What enhances the ability of phagocytes to recognize and engulf pathogens?
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How does the spacing of mannose and fucose residues affect MBL binding?
How does the spacing of mannose and fucose residues affect MBL binding?
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What component of the complement system forms the membrane attack complex?
What component of the complement system forms the membrane attack complex?
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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).
Dendritic Cells as Links
- 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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Description
Test your knowledge on the characteristics and functions of innate and adaptive immunity. This quiz covers key concepts like protective mechanisms, the roles of various immune cells, and the differences between innate and adaptive responses. Perfect for students studying immunology or biology!