2. Innate Immunity Flashcards

1
Q

What is innate immunity?

A

Immunity which is not intrinsically affected by prior contract with infectious agents
- “non-specific” antimicrobial systems
- localized
- ready to go; all the components needed are already there, they just need to be expressed (this also means how you respond today is likely how you’ll respond in a few months)

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2
Q

What are 3 representative mechanisms of innate immunity?

A
  1. Phagocytosis
  2. Complement cascades
  3. Neutrophil NET formation
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3
Q

What are 3 different ways to group immune system responses?

A
  1. Innate vs. adaptive
  2. Humoral vs. cell-mediated
  3. Local vs. systemic
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4
Q

What are the 7 key steps in the phagocytic process?

A
  1. Chemotaxis
  2. Adherence: receptor binding and recognition
  3. Receptor activation: cross-linking and overcoming threshold of activation
  4. Induction of phagocytic signaling cascades
  5. Pseudopod formation and internalization
  6. Initiation of intracellular degradative mechanisms, killing responses, and release of pro-inflammatory mediators
  7. Digestion and release of degradation products
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5
Q

Evolution of phagocytosis
- What was it originally developed for?
- Driver for immune roles?

A
  • Originally developed not for immune protection, but for control of normal cellular turnover. This dates back to multicellular bacterial biofilms. It is only over millions of years of evolution that tis has developed into a key innate antimicrobial mechanisms
  • Driver for immune roles: intracellular growth of internalized microorganisms had to be controlled to prevent overwhelming of host. Pathogen innate immune recognition also needed to develop
  • Highly conserved over millions of years of evolution because of its contributions to host defenses and maintenance of homeostasis
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6
Q

What cells display phagocytosis?

A

Professional phagocytes: monocytes, macrophages, immature dendritic cells, neutrophils
- different phagocytes have applied phagocytosis to different fxn

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7
Q

What is the major difference between professional and nonprofessional phagocytes?

A

Phagocytic efficiency and capacity differs due to an array of phagocytic receptors that increase particle range and phagocytic rate

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8
Q

What are 3 survival strategies used by intracellular pathogens?

A
  1. Prevent fusion of lysosomes to the phagosome
  2. Escape from phagosome before fusion of lysosomes
  3. “Tough-it-out” within the phagolysosome
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9
Q

Phagocytosis vs. Endocytosis vs. Pinocytosis

A

Phagocytosis: Internalization of particles that are bigger than 1 micron in diameter
- Receptor-mediated
- eg. bacteria, apoptotic cells
- Involved in immunity

Endocytosis: Internalization of particles smaller than 1 micron in diameter
- Receptor-mediated
- eg. viruses, small immune complexes
- Involved in down-regulation of surface receptors, nutrient uptake and synaptic vesicle recycling

Pinocytosis: “cell drinking” - Non-receptor mediate (non-specific)
- Involved in the uptake of fluid and soluble molecules from extracellular environment

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10
Q

What are the 2 types of phagocytic receptors?

A
  1. Direct recognition (eg. scavenger or mannose receptors)
  2. Indirect recognition (eg. antibodies, complement, focolins and collectins)

*Phagocytes contain many receptors. A number of them are involved in innate immunity (eg. TLRs). Only a fraction of them are phagocytic receptors.

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11
Q

Affinity

A

Strength of a noncovalent binding interaction; the higher the affinity the higher likelihood 2 partners will exist in a complex

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12
Q

Avidity

A

Increased “apparent” affinity of a molecule for its ligand due to the presence of multiple binding sites on both partners

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13
Q

Phagolysosome formation

A
  • Once target is bound and the activation signals have been provided the phagosome must be taken into the cell
  • Requires actin rearrangements, myosin interaction with actin (stimulates entry), and dynamin (helps contract and pinch off the membrane
  • ## Phagosome fuses with primary, secondary granules, and lysosomes forming a destructive phagolysosome
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14
Q

What are reactive oxygen and nitrogen species used for?

A

To kill internalized microorganisms (don’t want the pathogen to survive in the phagocyte)
- highly corrosive and very toxic

Reactive oxygen intermediates (ROI) = “one punch”
- produced in the phagolysosome by NADPH oxidase (premade components) quite rapidly
- bc they are premade, they are limiting

Reactive nitrogen intermediates (RNI) = “two punch”
- produced in the cytoplasm and then diffuses into the phagosome to react with internalized microbes
- slower and long-lasting

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15
Q

What drives a pro- vs anti-inflammatory cellular program during phagocytosis?

A
  1. Phagocyte + Pathogen = Pro-inflammatory
  2. Phagocyte + Apoptotic body = Anti-inflammatory
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16
Q

Phagocytosis of apoptotic cells is usually…

A

Anti-inflammatory

17
Q

Apoptosis

A

Mechanism to get rid of spent cells without causing unwanted inflammation
- Activation of specific proteases and nucleases lead to death
- Phagocytosis results in the release of anti-inflammatory mediators

18
Q

Live erythrocytes are not removed from the bloodstream prematurely, how? What cells are known to remove senescent erythrocytes?

A

CD47 is a receptor expressed on the surface of HEALTHY erythrocytes; it binds to an immunoglobulin family receptor SIRP-1a on the macrophage surface. Binding increases the threshold of activation needed to induce phagocytosis.

Kupffer cells and splenic macrophages are known to remove senescent erythrocytes from the liver and spleen, respectively.

19
Q

What is system lupus erythematosus (SLE) characterized by? How can a single disease lead to such a broad range of symptoms?

A

Characterized by formation of autoantibodies to self antigens
- Primarily against nucleic acid

  1. Immune complexes are deposited in wall of blood vessel
  2. Presence of immune complexes activates complement and attracts inflammatory cells such as neutrophils
  3. Enzymes released from neutrophils cause damage to endothelial cells of basement membrane
20
Q

How do phagocytes play a role in prion disease such as BSE and CWD?

A

Prions have to be ingested orally then make it to the CNS of the animal, this is a 2 step process:
1. Phagocytes
- internalize prions, that have a high B-sheet content making them difficult to digest so they go with the phagocytes to the spleen where prions are released
2. Hematopoiesis