Introduction Flashcards

1
Q

Immune Response

Definition

A
  • Maintain a state of homeostasis such that when the system is perturbed by a foreign invader (external or internal) an adequate response is generated to control the invader
  • Then the system returns to equilibrium.
  • It’s memory of that particular invader is retained so that a more rapid and heightened response will occur should the invader return
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2
Q

External Threats

A
  1. Microorganisms
    • Bacteria
    • Viruses
    • Fungi
  2. Parasites
    • Protozoa
    • Worms
    • Ectoparasites
  3. Mechanical or chemical trauma
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3
Q

Internal Threats

A
  1. Cancerous cells
  2. Abnormal cells
  3. Old or damaged cells
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4
Q

Mechanisms of Defense

A
  1. Exterior Barrier
  2. Innate immune response
  3. Adaptive immune response
  4. Memory
    • Prevents reinfection or recurrence of illness
    • Maintained by adaptive immunity
    • Functionally combines both innate and adaptive immunity
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5
Q

Exterior Defense Mechanisms

A

Provides a natural barrier that:

  1. Prevents microbial colonization
  2. Prevents host invasion

Microorganisms generally need to adhere to/penetrate host tissues and proliferate at that time to induce disease.

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6
Q

Mechanical Barriers

A

Contribute to defense by inhibiting attachment and penetration of infectious agents.

  • Skin
  • Mucus
  • Cilia lining mucosa (mucociliary elevator)
  • Mechanical
    • Coughing
    • Sneezing
    • Peristalsis
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7
Q

Chemical Barriers

A

Numerous components of bodily secretions contain microbicidal factors.

  • Sweat and sebaceous secretions
    • Contain lactic acid and fatty acids
  • Lysozyme
    • Present in tears, saliva, and nasal secretions
    • Hydrolyzes bacterial cell wall
  • Acidic environments
    • Urine and vaginal secretions
    • Hydrochloric acid in stomach
  • Lactoferrin and transferrin
    • Iron chelators
  • Defensins
    • In the lung and GI tract
    • Damages microbial membranes
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8
Q

Bacterial Interference

A
  • Normal flora colonizes:
    • Upper respiratory
    • Lower GI
    • Reproductive tracts
    • Skin
  • Competes with pathogens for nutrients and for attachment sites on epithelial or mucosal surfaces
  • Potent barrier to the establishment of infection by pathogens
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9
Q

Microbial Invasion

A

Pathogens can evade, overwhelm, or penetrate a barrier.

After entry into the host it begins to replicate.

Body generates an immune response.

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10
Q

Immune Response

Overview

A

Innate Immunity

  • Ready to function prior to exposure to the threat ⇒ rapid response
  • Attempts to control and/or eliminate the threat
  • If unable to eliminate the threat, the goal is to keep the body alive long enough for the adaptive response to occur

Adaptive Immunity

  • Activated if innate immunity has failed to eliminate the threat
  • Threat has bypassed an “activation threshold”
  • Includes mechanisms that require days to weeks to become fully functional
  • Usually capable of eliminating the threat
  • Establishes long-term memory
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11
Q

Innate Immunity

Overview

A
  • Functions by means of pre-existing antimicrobial molecules and cells
  • Can resolve most insults
  • Only has a few types of recognition molecules that recognize common motifs to many different pathogens
  • Can use components of the adaptive immunity to target their immune response
    • Antibodies & Cytokines
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12
Q

Innate Immunity

Components

A
  1. Phagocytic cells
    • Neutrophils
    • Macrophages
    • Natural killer (NK) cells
  2. Several cytokines
  3. Complement
  4. Multiple plasma proteins
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13
Q

Innate Immune Response

Goals

A
  1. Kill/remove the threat
  2. If unable to remove threat, amplifies and stimulates the immune response
  3. Prevent spread of the threat
  4. Prepare for the adaptive immune response
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14
Q

Cytokine

Definition

A
  • A mediator that influences the growth, differentiation, or function of cell types inside and outside of the immune system
  • Made by cells of the immune system and other cells in the body
  • Usually a soluble glycoprotein that binds to specific receptors to induce signaling
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15
Q

Tissue Macrophages

A

There are two major types of tissue macrophages:

  • Resident macrophages
    • Microglia
    • Kupffer cells
    • Alveolar macrophages
    • Osteoclasts
  • Proinflammatory macrophages
    • Recruited from the blood during an immune response
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16
Q

Neutrophils

(PMNs)

A
  • Granulocytes that circulate in the blood
  • Migrate quickly in response to local stimulation or invasion by a microorganism
  • Critical to immune defense against extracellular bacteria & other threats
17
Q

Antigen

A

Any molecule that can bind specifically to an antigen receptor (e.g. antibody, TCR)

Pathogens are usually composed of many repeating antigentic components.

18
Q

Epitope

A

The site on an antigen that is bound by an antibody or TCR

(a.k.a. antigenic determinants)

Many/most antigens have more than one epitope

19
Q

Methods of Recognition

A
  • Both Ig and TCR contain:
    • a variable antigen-binding domain
    • a constant region
      • Important in anchoring it to the cell
      • Gives it certain effector properties
  • Characteristics of B and/or T cell responses:
    • Specific for initiating antigen
    • Each receptor varies slightly in structure giving it a different reactivity
    • Each B or T cell only expresses a single antigen receptor
20
Q

Immunoglobulins

(Ig)

A

Expressed by B-cells:

  • B cell receptor (BCR)
    • Membrane bound Ig that determines the antigen specificity of the B cell
    • BCR can bind free antigen (native and/or denatured)
      • Protein
      • Polysaccharide
      • Lipid
      • Nucleic acid
  • Antibodies (Ab)
    • Soluble forms of immunoglobulins
    • Secreted by plasma cells
    • Exerts different effector functions
21
Q

TCR

(T cell receptor)

A
  • Membrane-bound antigen receptor expressed by T-cells
  • TCR cannot bind to free antigen
  • Only recognizes peptide antigens presented by major histocompatibility molecules
    • Class I MHC
    • Class II MHC
  • Means T-cells are stimulated by host cells expressing MHC and foreign antigens but not free antigen
22
Q

Lymphoid Organs

A
  1. Primary lymphoid organs
    • generative organs
    • B lymphocytes (B cells) - bone marrow
    • T lymphocytes (T cells) - thymus
  2. Secondary lymphoid organs
    • Highly organized tissues that promote the interaction between antigen, T cells, and B cells.
    • Naive T and B cells are usually activated here then proliferate, differentiate, and promote effector functions
    • Includes:
      • Lymph nodes
      • Spleen
      • MALT (mucosal-associated lymphoid tissue)
        • BALT (bronchial-associated lymphoid tissue)
        • GALT (gut-associated lymphoid tissue)
23
Q

Clonal Proliferation

A
  • Usually a threat will activate the few cells that can recognize it out of the millions of different antigen receptors
  • Cells stimulated to divide, proliferate, and differentiate into effector cells.
  • Daughter clones have the same antigenic specificity as the parental cell.
24
Q

Helper T-cells

(TH)

A
  • Express CD4+ markers
  • Synthesize cytokines
    • Modulate the immune system
    • Helps immune system to function
  • Critical role in promoting most adaptive and many innate immune responses
  • Promotes immunity to both intracellular and extracellular threats
25
Q

Cytotoxic T Cells

(TC)

A
  • Express CD8+ surface markers
  • Kill cells by direct cell-cell contact if TCR is properly engaged
  • Produce a limited cytokine profile
  • Plays a major role in immunity against intracellular threats
    • Viruses
    • Abnormal cells/cancer
    • Some intracellular bacteria
26
Q

B lymphocytes

A
  • Produce antibodies that plays a role in:
    • Eliminating extracellular microorganisms
    • Neutralizing soluble toxins
27
Q

Antibody

Isotypes

A
  • There are different major classes of antibodies.
  • Each isotype can be characterized by:
    • Structure
    • Location
    • Effector functions
  • Some isotypes promote unique intracellular actions through Fc receptors
28
Q

Extracellular Bacteria

Immune Response

A
  • Complement
  • Macrophages
  • Neutrophils
  • Proinflammatory response
  • Antibodies (adaptive)
  • +/- TH cells (adaptive)
29
Q

Intracellular Bacteria

Immune Response

A
  • Macrophages
  • TH cells (adaptive, IFN-γ)
30
Q

Viruses

Immune Response

A
  • Select cytokines
    • Type I Interferons (IFN-α and IFN-β)
    • Natural killer cells (NK cells)
    • Cytokine production by T-helper cells (adaptive)
    • Killing by cytotoxic T-cells (adaptive)
    • Less of a role:
      • Complement
      • Macrophages
      • Neutrophils
      • Proinflammatory cytokines
31
Q

Helminthic Parasites

Immune Response

A
  • Eosinophils
  • Mast cells
  • Basophils
  • IgE (adaptive immunity)
  • TH cells (adaptive)
32
Q

Phases of the

Immune Response

A
  1. Recognition Phase
    • Innate Immunity
      • Receptors bind common pathogenic motifs
        • lipopolysaccharide (LPS)
        • mannose
        • C-polysaccharide
      • Recognizing other components of the immune response:
        • antibodies
        • cytokines
        • products of innate immunity
    • Adaptive immunity
      • Antigen specific receptors
  2. Amplification Phase
    • Innate Immunity:
      • Cascades (complement)
      • Secretion of soluble mediators
        • Cytokines
        • Acute phase proteins
      • Recruitment of an “army of cells”
        • Neutrophils
    • Adaptive Immunity:
      • Lymphocyte proliferation and differentiation into effector cells
  3. Effector Phase
    • Elimination of antigen by one of many mechanisms
      • Phagocytosis
      • Lysis
      • Neutralization
      • Killing by cytotoxic T-cells
  4. Termination Phase
    • A number of mechanisms down regulate the immune system after antigen has been removed
    • Very important because an improperly regulated immune response can cause extensive tissue damage
  5. Memory
    • Adaptive
    • Facilitates innate processes
    • Long-lived memory T and B cells are generated
    • Memory cells have lower threshold for activation
      • React faster
      • Shows amplification
      • “Mature” response where Ab generated
    • Residual components (antibodies) are immediately available