Immuno: Immune response to infection Pt.1 Flashcards

1
Q

What are the two main routes of infections of pathogens?

A
  • External epithelia (e.g. skin)
  • Mucosal surfaces (e.g. GI tract)
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2
Q

List some features of skin that makes it an effective barrier to infection.

A
  • Consists of tightly-packed keratinised cells
  • Low pH
  • Low oxygen tension
  • Sebaceous glands
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3
Q

What do sebaceous glands produce that has antibacterial effects?

A
  • Hydrophobic oils - repels water and microorganisms
  • Lysozyme - destroys the structural integrity of the bacterial cell wall
  • Ammonia and defensins - anti-bacterial properties
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4
Q

Describe the defensive features of mucosal surfaces.

A
  • Traps invading pathogens
  • Cilia promote the removal of mucus
  • Contains secretory IgA which binds to pathogens and prevents them from attaching to and penetrating epithelial cells
  • Contains lysozyme and other antimicrobial peptides
  • Lactoferrin starves invading bacteria of oxygen
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5
Q

How do commensal bacteria act as a barrier to infection?

A

Competes with pathogenic bacteria and produces various antimicrobial agents

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6
Q

List the cells of the innate immune system.

A
  • Polymorphonuclear cells
  • Monocytes/macrophages
  • NK cells
  • Dendritic cells
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7
Q

List the soluble components of the innate immune system.

A
  • Complement
  • Acute phase proteins
  • Cytokines and chemokines
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8
Q

List some key features of cells of the innate immune system.

A
  • Identical responses in all individuals
  • Cells express genetically-encoded receptors (PRRs) that allow them to detect pathogens at the site of infection
  • Cells have phagocytic capacity
  • Cells secrete mediators (e.g. cytokines/chemokines) that regulate the immune response
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9
Q

Name the resident macrophage in the following tissues/organs:

  1. Liver
  2. Kidney
  3. Bone
  4. Spleen
  5. Neural tissue
  6. Connective tissue
  7. Skin
A
  1. Liver = Kupffer cells
  2. Kidney = Mesangial cells
  3. Bone = Osteoclasts
  4. Spleen = Sinusoidal lining cells
  5. Neural tissue = Microglia
  6. Connective tissue = Histiocytes
  7. Skin = Langerhans cells
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10
Q

How do macrophages differ from polymorphonuclear cells?

A

They can process antigens and present them to T cells

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11
Q

Outline the process of phagocyte recruitment in response to infection.

A
  • Cellular damage and bacterial products trigger the production of inflammatory mediators (cytokines and chemokines)
  • Cytokines enhance vascular permeability
  • Chemokines attract phagocytes (chem = chemistry = attract)
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12
Q

Describe how cells of the innate immune system recognise pathogens.

A
  • Neutrophils mobilised very quickly from BM and migrate to site of infection
  • Pattern-recognition receptors (PRRs) recognise generic motifs called PAMPs (e.g. bacterial sugars, DNA and RNA)
  • Fc receptors on these cells allow binding to the Fc portion of immunoglobulins thereby allowing phagocytosis of immune complexes
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13
Q

What are examples of PRRs?

A
  • Toll-Like Receptors (TLRs)
  • Mannose Receptors
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14
Q

What is opsonisation?

A

The molecular mechanism that uses opsonins to make a molecule (e.g. antigen) more palatable to the phagocyte.

I.e. opsonins act as a bridge between the pathogen and the phagocyte receptors

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15
Q

Which other factors can bind to phagocytes to facilitate phagocytosis?

A
  • Complement components (e.g. by binding to CR1)
  • Acute phase proteins (e.g. CRP)
  • Antibodies
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16
Q

Describe the formation of a phagolysosome

A
  • Pathogen taken up into phagosome
  • Fuses with lysosome
  • Forms phagolysosome

> > Protected compartment in which killing of organism occurs

17
Q

Describe the reactions involved in oxidative killing of pathogens within phagolysosomes.

A
  • NADPH oxidase converts oxygen into reactive oxygen species (e.g. superoxide and hydrogen peroxide)
  • Myeloperoxidase catalyses the production of hypochlorous acid (from hydrogen peroxide and chloride)
18
Q

What is non-oxidative killing?

A
  • Killing by the release of bactericidal enzymes (e.g. lactoferrin, lysozyme)
19
Q

Why do neutrophils die after phagocytosis? What does this form?

A
  • Phagocytosis depletes the glycogen stores of the neutrophil resulting in neutrophil death
  • The accumulation of dying neutrophils forms pus
20
Q

How do NK cells determine whether to lyse cells or not?

A
  • They have inhibitory receptors which recognise self HLA and they have activating receptors that recognise heparan sulphate proteoglycans
  • The balance of these signals determines the response
  • I.e. if HLA downregulated, activatory signal will become dominant
  • They kill ‘altered self’ cells (e.g. malignancy or virus-infected cells)
21
Q

Describe the main features of dendritic cells.

A
  • Reside in peripheral tissues
  • Express receptors for cytokines/chemokines
  • Express pathogen recognitiion receptors
  • Express Fc receptors for immunoglobulin
  • Capable of phagocytosis
  • Present processed antigens to T cells in lymph nodes to prime the adaptive immune response
22
Q

What does a dendritic cell do after phagocytosis?

A
  • Upregulate expression of HLA molecules
  • Express co-stimulatory molecules
  • Migrate via lymphatics to lymph nodes
23
Q

Which receptor is involved in the migration of dendritic cells to lymph nodes?

A

CCR7

24
Q

What is the difference between primary and secondary lymphoid organs?

A
  • Primary - involved in lymphocyte development (bone marrow and thymus)
  • Secondary - anatomical sites of interaction between naïve lymphocytes and microorganisms (e.g. spleen, lymph nodes, MALT)
25
Q

What is a germinal centre?

A

Area within a secondary lymphoid organ where B cells proliferate and undergo affinity maturation and isotype switching

26
Q

What are the components of the adaptive immune response?

A
  • ‘Humoral immunity’ - B lymphocytes and antibodies
  • ‘Cellular immunity’ - T lymphocytes (CD4 and CD8 cells)
  • Soluble components - cytokines and chemokines