Unit 3: Immunology Flashcards

1
Q

Define “immunity”.

A

the ability of the body to protect itself

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2
Q

Define “non-specific defense” and “specific immune response”.

A

non-specific: innate; not specific to any one pathogen

specific: acquired immunity; develop when exposed to pathogen; adaptive - different each time.

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3
Q

Describe the physical and chemical barriers of the first line of defense.

Provide some examples.

A

physical- skin, mucosae, mucus, secretions

chemical- enzymes, antibodies, pH

also mechanical- flushing, fluid flow

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4
Q

Describe the different components of the second line of defense:

NON-SPECIFIC.

[5]

A

Phagocytes: can envelop pathogen by endocytosis and ingest it > cellular digestion

Inflammation/Fever: will draw fluid and phagocytic WBC into infection area & enhance capacity for stopping infection at this site through focal attack

Complement system: a series of proteins that work as a cascade to eventually form open holes on any bacterial cell membranes & enveloped viral particles > cell lysis/inflammation/opsonization

Interferon: decrease transcription/translation > protect against viruses

Natural Killer/ NK Cells: lymphocyte type; interact with infected cells and release toxin (perforin) that will perforate pathogenic cell & disrupt membrane > cell lysis

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5
Q

Describe the characteristics that define a specific immune response.

a. Specific
b. Recognition of Self
c. Memory
d. Versatility

A

Specific- WBC and antigen fit together perfectly like lock and key

Recognition of self- cells recognize themselves to prevent WBC attack against our own healthy cells

Memory- once you made multiple WBC copies unique to a pathogen, easier to make more copies during future exposure

Versatility- potential for antigen recognition is almost unlimited

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6
Q

Define and describe “antigen” and “antibody”.

A

antigen: usually a protein; foreign substance, ( like virus, bacterium..) that can stimulate an immune response in the body.

antibody: AKA immunoglobulin; protein produced by the immune system in response to the presence of an antigen.
~designed to specifically target and neutralize antigens, helping the immune system defend the body against infections and diseases.

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7
Q

Describe the cells of specific immunity. What is their structure, where do they originate, what is their role in specific immune reactions?

A
  1. Antigen presenting cell APC
    AKA macrophage in tissue/ monocyte in blood
    ~aggresive phagocyte
    ~capture, process, and present antigens to helper T cells
  2. T-lymphocytes [cell-mediated]
    ~derive from stem cell lymphocytes
    ~differentiate into 3 subtypes
    a. cytotoxic/ killer T lymphocyte- bind to antigens and secrete perforins
    b. helper cells - activate other lymphocytes to enhance response
    c. Regulatory/suppressor cells- suppress lymphocytes to prevent excessive immune response
  3. B-lymphocytes (humoral immunity)
    ~split into 2 types
    a. plasma cells (produce antibodies > immunological response)
    b. memory cells (prolonged immunity to pathogen exposure)
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8
Q

Compare and contrast cell-mediated and humoral immunity.

A

Cell-Mediated Immunity:

Involves T lymphocytes
works against cellular pathogens (bacterial cells, not against viruses, but works with virus-infected cells).

Humoral Immunity:

Involves B lymphocytes
Provides immunity against cellular and non-cellular pathogens including viruses

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9
Q

Describe the predominant way in which T-cells are activated

A

Via macrophage or infected cell

APC will digest pathogen, take antigenic pieces and place them inside cell membrane; Helper T cells latch on and produce a chemical signal that will stimulate any other T cells that also recognized the antigen

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10
Q

Describe the different T-cell types produced during the proliferative phase:

a. Helper T-Cells
b. Cytotoxic T-Cells
c. Suppressor T-Cells
d. Memory T-Cells

A

a. Helper T-Cells- multiply and secrete cytokines that summon macrophages and cytotoxic T cells to the infected site.

b. Cytotoxic T-Cells- kill toxic/target cells

c. Suppressor T-Cells- stopping an autoimmune response once the threat has been eliminated.

d. Memory T-Cells- critical role in long-term immunity. They “remember” previous encounters with specific antigens and respond more rapidly and effectively upon re-exposure to the same pathogen.

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11
Q

Describe the mechanism for T-cell destruction of pathogens.

What type of pathogens are T-cells effective against?

A

~Effective against intracellular pathogens (bacterial cells, not against viruses, but works with virus-infected cells).

T cells can wipe out infected/cancerous cells; also direct immune response by helping B lymphocytes eliminate invading pathogens.

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12
Q

Describe the two predominant ways in which B-cells are activated (T-cell dependent and independent).

A

T-Cell-Dependent Activation:
B cells need help from Helper T cells, which recognize the antigen presented by B cells and provide cytokines (signaling molecules) that activate B cells

T-Cell-Independent Activation:
B cells can activate themselves when they directly bind to simple antigens.

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13
Q

Describe the mechanism for B-cell destruction of pathogens.

What type of pathogens are B-cells effective against?

A

~Primarily effective against extracellular pathogens (viruses, bacteria, toxins..)

B cells create APCs/ antibodies >antibodies bind to pathogens/foreign substances, such as toxins, to neutralize them.

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14
Q

Compare and contrast active and passive immunity.

A

active- body exposed to pathogen and produces own antibodies
[getting sick or vaccination]

passive- we acquire antibodies made by another organism
[through placenta/breastfeeding or immunotherapy]

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15
Q

what is the immune system?

A

Our defensive system

defending us against foreign materials (pathogens) - [bacteria, viruses, etc.]

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16
Q

The first line of defense includes:

A

Physical barrier of skin [unless broken, effective]

Chemical barrier [secretions…]
~skin & mucus membranes
~Respiratory/ GI tract

17
Q

a. Phagocytes
b. Inflammation and Fever
c. Complement System
d. Interferon
e. Natural Killer Cells (NK Cells)

These are all components of : ?

A

2nd line of defense

[not specific]

18
Q

T-lymphocytes [cell-mediated]

Where to they derive from?

what are the 3 sub types?

A

~derive from stem cell lymphocytes

a. cytotoxic/ killer T lymphocyte- binds to antigens and secrete perforins

b. helper cells - activate other lymphocytes to enhance response

c. Regulatory/suppressor cells- suppress lymphocytes to prevent excessive immune response

19
Q

5 basic Steps of Acquired/Specific Immunity

A
  1. activation
  2. proliferation
  3. attack phase
  4. suppression
  5. memory
20
Q

Immunization is an effective way to enhance the immune systems ability to provide protection from pathogen exposure.

describe how immunization provides protection to future exposure to a pathogen.

A

Immunization triggers a specific immune response that produces memory cells.

Future exposure to the pathogen will trigger these memory cells resulting in quick activation and exaggerated proliferation of immune cells specific for the pathogen.

21
Q

The immune cell type responsible for “cell mediated” immunity:

A

T-lymphocte

22
Q

Which of the following cells is NOT a cellular member of the acquired immune response:

tissue macrophage
plasma cell
natural killer cell
T-lymphocyte

A

natural killer cell

[2nd line]

23
Q

The cell responsible for phagocytizing pathogens and presenting their antigens for initiation of a specific immune response is

A

tissue macrophage
monocyte
antigen presenting cell

24
Q

The first line of immunological defense includes:

[2 types with example]

A

physical barriers, such as the skin

chemical barriers, such as stomach secretions

25
Q

When antibodies bind to the surface of a pathogen they increase the likelihood that a phagocyte will attach to and then phagocytize the pathogen. This is called:

A

opsonization

26
Q

Antibodies can bind to:

A

two identical antigens at a time

27
Q

Antibodies may contribute to the destruction of pathogens by:

[5 ways]

A

attracting phagocytes by chemotaxis
opsonizing pathogens
precipitating soluble pathogens
agglutinating the pathogen
neutralizing the pathogen

28
Q

The Complement System combats invading pathogens by all of the following EXCEPT:

opsonizing pathogens
binding antigens together causing agglutination
lysing infected cells
stimulating mast cell secretion of histamine
lysing pathogens

A

binding antigens together causing agglutination

29
Q

_______________ : interact with infected cells and release toxin (perforin) that will perforate pathogenic cell & disrupt membrane > cell lysis

A

Natural Killer/ NK Cells

[2nd line of defense]

30
Q

NK cells are part of which defense?

A

2nd line

31
Q

__________: decrease transcription/translation > protect against viruses

A

Interferon

[2nd line of defense]

32
Q

_____________________ : a series of proteins that work as a cascade to eventually form open holes on any bacterial cell membranes & enveloped viral particles > cell lysis/inflammation/opsonization

A

Complement system

[2nd line of defense]

33
Q

_____________ : can envelop pathogen by endocytosis and ingest it > cellular digestion

A

Phagocytes

[2nd line of defense]

34
Q

Phagocytes are part of which defense?

A

2nd line

35
Q

Chronotropic effects are :

A

those that change the heart rate