Immune Flashcards

1
Q

Compare and contrast innate (nonspecific) defenses with adaptive (specific) defenses. Do they attack healthy or infected cells? Do they need priming? What do they both do?

A

Innate

  • attacks anything that does not have your genetic code
  • Natural killer cells also take out healthy cells in the process

Adaptive

  • T/B lymphocytes fights off particular pathogen, involves antibodies
  • T cells fight just infected cells
  • must be primed by initial exposure

Both
-Protects against infectious agents and abnormal body cells

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2
Q

What are the 2 lines of defense for the innate defense system? What is the 3rd line of defense? Which one is faster? - chart

A

First - external body membranes
Second - internal defense
Third - adaptive immune system (T/B cells)
-innate system faster

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3
Q

What are the 5 components of an internal (second line) defense of the innate immune system?

A

antimicrobial proteins, phagocytes, and NK cells, inflammation, fever

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4
Q

What are some Protective chemicals that inhibit or destroy microorganisms on the skin? (7)

A

Acidity of skin and secretions – acid mantle – inhibits growth
Enzymes - lysozyme of saliva, respiratory mucus, and lacrimal fluid – kill many microorganisms
Defensins – antimicrobial peptides – inhibit growth
Other chemicals - lipids in sebum, dermcidin in sweat – toxic

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5
Q

What are the mucosa protectors? (2)

A

Mucus-coated hairs in nose

Cilia of upper respiratory tract

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6
Q

What are the surfaces barriers ward off invading pathogens? (3)

A

Skin, mucous membranes, and their secretions

  • Physical barrier to most microorganisms
  • Keratin resistant to weak acids and bases, bacterial enzymes, and toxins
  • Mucosae provide similar mechanical barriers
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7
Q

What is opsonization?

A

phagocytes marks pathogens—coating by complement proteins or antibodies so they can undergo phagocytosis

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8
Q

What are the steps of phagocytosis? What are the 2 types of phagocytes?

A

neutrophils and macrophages

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9
Q

What is the function of natural killer cells? (3)

A
  • Attack cells that lack “self” cell-surface receptors (MHC)
  • Induce apoptosis in cancer cells and virus-infected cells
  • Secrete potent chemicals that enhance inflammatory response
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10
Q

What is the purpose of the inflammatory response? (4) When is it triggered?

A

Prevents spread of damaging agents
Disposes of cell debris and pathogens
Alerts adaptive immune system
Sets the stage for repair

-Triggered whenever body tissues injured

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11
Q

What are the steps of neutrophil mobilization? What follows them?

A

Neutrophils lead; macrophages follow, then monocytes

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12
Q

Describe the steps of inflammatory response - chart.

A
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13
Q

Why can inflammation be beneficial?

A

inflammation causes area to swell with white blood cells that phagocytize pathogens and cleans the area for healing

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14
Q

Describe the mechanism of fever and the role of pyrogens.

A
  • Leukocytes and macrophages secrete pyrogens

- Pyrogens act on body’s thermostat in hypothalamus, raising body temperature

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15
Q

Explain why fever can be beneficial. (High and moderate)

A

moderate

  • Causes liver and spleen to sequester (hold onto) iron and zinc (needed by microorganisms)
  • Increases metabolic rate → faster repair

high
-high fever kills microorganisms

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16
Q

What are the 3 main characteristics of adaptive defense?

A

Specific – recognizes and targets specific antigens
Systemic – not restricted to initial site
Have memory – stronger attacks to “known” antigens

17
Q

What are the 2 arms of adaptive defense and how are they different?

A

Humoral (antibody-mediated) immunity

  • antibodies circulate freely
  • mark target cell for destruction
  • extracellular targets
  • antibodies produced by B cells (that stay in lymph node) go out

Cellular (cell-mediated) immunity

  • directly kill infected cell or
  • indirectly release chemicals that enhance inflammatory response/activate other lymphocytes or macrophages
  • cellular targets
  • T cells directly go to site of infection
18
Q

What is immunogenecity vs reactivity of complete antigens?

A
  • immuno = ability to stimulate proliferation of lymphocytes

- reactivity = ability to react with activated lymphocytes and antibodies released

19
Q

What is the difference between complete and incomplete antigens? What are incomplete antigens called? What are some examples?

A
  • incomplete antigens = haptens
  • (haptens) not immunogenic by themselves but is if attaches to body proteins
  • complete ex - protein, lipids, polysach, nucleic acid
  • hapten ex - poison ivy, detergents, cosmetics, animal dancer
20
Q

What are antigenic determinants? How much do most have?

A
  • certain parts of entire antigen are immunogenic

- Most antigens have several different antigenic determinants.

21
Q

What are self-antigens? What is an example? What does it do?

A
  • Protein molecules (self-antigens) on surface of cells not antigenic to self but antigenic to others in transfusions or grafts
  • MHC unique to individuals
  • MHC of APC presents antigens to T lymphocyte to start immune resposne
22
Q

What are the steps to lymphocyte development, maturation, and activation?

A

immunocompetance = ability to recognize specific antigen
self tolerance = unresponsive to own antigen
effector cells = fight antigen

23
Q

Describe the immunological memory (anamnestic) response.

A

primary immune response - Cell proliferation and differentiation upon first antigen exposure. lag period then peaks

Secondary immune response - Re-exposure to same antigen gives faster, more prolonged, more effective response. responds within hours

24
Q

What are the 2 types of active humoral immunity?

A

Naturally acquired—response to bacterial or viral infection

Artificially acquired—response to vaccine of dead or attenuated pathogens

25
How do vaccines work?
- Most of dead or attenuated (inactivated) pathogens - Spare us symptoms of primary response - Provide antigenic determinants that are immunogenic and reactive
26
What is passive humoral immunity? Are B cells challenged by antigens? Does immunological memory occur? Does protection end?
-Readymade antibodies introduced into body -B cells are not challenged by antigens Immunological memory does not occur Protection ends when antibodies degrade
27
What are the 2 types of passive humoral immunity?
Naturally acquired—antibodies delivered to fetus via placenta or to infant through milk Artificially acquired—injection of serum, such as gamma globulin
28
Humoral immunity types chart
29
What are the 3 kinds of antigen presenting cells? (APC) What do they do?
- dendritic, macrophages, B cells | - engulf & present antigens to T cells for recognition
30
Why can inflammation be beneficial? (3) Is it beneficial in the long-run?
- swelling causes pressures on nerves that causes pain and alerts injury - body slows down so focus energy on healing - WBC, haptens, antibodies all come to the site of infection - not beneficial in long run because disrupts organ function
31
Provide specific examples to demonstrate how the lymphatic system responds to maintain homeostasis in the body.
-innate and adaptive immunity work to bring body back to non-infected state
32
Explain how the lymphatic system relates to other body systems to maintain homeostasis.
- parasympathetic system activated to focus energy on repair | - other systems do not functions as well
33
Predict the types of problems that would occur in the body if the lymphatic system could not maintain homeostasis.
- constantly getting sick because no immune system to fight back - can be killed
34
Predict factors or situations affecting the lymphatic system that could disrupt homeostasis.
-pathogens, tylenol (disrupts fever)