Section 5 Review Flashcards

1
Q

Bacteria normally found at various non-sterile body sites are called

A

commensal organisms

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2
Q

The consortium of colonizing microbes has been dubbed the human ________ or ________

A

microbiota or microbiome

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3
Q

What are the benefits of Commensals

A
  1. Make vitamins and digest food
  2. Prevent colonization by pathogens (compete with them for food and produced antibacterial agents that kill them)
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4
Q

What are the risks of commensals

A
  • might cause disease in immunocompromised patients
  • anaerobic gas gangrene if it gets in surrounding tissues
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5
Q

What is the specificity of innate or non-adaptive immunity

A

non-specific

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6
Q

When does innate or non-adaptive immunity occur

A

present at birth

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7
Q

Does innate immunity have memory

A

no

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8
Q

What cells are involved with innate immunity

A

antigen-present cells such as macrophages

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9
Q

What is the specificity for adaptive immunity

A

specifc

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10
Q

When does adaptive immunity occur

A

upon exposure to antigens

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11
Q

Does adaptive immunity have memory

A

yes, faster response upon second exposure

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12
Q

What type of cells are involved with adaptive immunity

A

T-cells and B-cells

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13
Q

What are the types of adaptive immunity

A
  • Humoral immunity (mediated by B-cells and activated by T-cells
  • Cell-mediated immunity (T-cells)
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14
Q

What are the Physical barriers in innate immunity

A
  1. skin - hard to colonize
  2. mucous membranes - mucous secreted traps pathogens
  3. lungs
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15
Q

What are the chemical barriers in innate immunity

A
  1. acidic pH of the stomach
  2. Lysozymes in tears
  3. Lysozyme in secreted mucous destroys pathogens
  4. defensins
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16
Q

What are macrophages considered to be

A

antigen-presenting cells

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17
Q

What are the signs of inflammation

A
  • swelling
  • redness
  • heat/fever
  • pain
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18
Q

What are the steps of inflammation in innate immunity

A
  1. macrophages phagocytose bacteria
  2. macrophages release chemicals to start inflammation
  3. more macrophages are called to the site of infection
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19
Q

How many serum proteins (complement factors) make up the complement cascade

A

20

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20
Q

What do complement factors do

A

attack bacterial invaders

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21
Q

What do complement factors do?

A

Attack bacterial invaders

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22
Q

Effective ness by which an antigen elicits an immune response

A

Immunogeniciy

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23
Q

What are the most effective antigens or the most immunogenic

A

proteins

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24
Q

Any molecule that when introduced in the body will elicit an immune response in the form of antibody production

A

antigen or immunogen

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25
Every antibody has a ________ ________ and a __________ ________
constant region, variable region
26
What do variable regions bind to
antigens
27
Every antibody has a tail known as the ___________, and two arms known as the _____________
Fc region, Fab regions
28
What are the 5 classes of antibodies
- IgG - IgM - IgA - IgD - IgE
29
Why are there 5 classes of antibodies
because of the differences in the constant regions
30
What does IgG contain
abundant in blood and tissue fluids
31
What does IgA contain
abundant in secretions such as tears and breast milk
32
What does IgM contain
first antibody detected during an immune response
33
When do antibodies appear in the blood in the primary antibody response
after several days
34
When do antibodies appear in the blood in the secondary antibody response
within hours due to memory from the first encounter
35
Which antibodies appear first in the primary antibody response
IgM and IgG
36
Which antibodies appear first in the secondary antibody response
IgG with a much higher response
37
What is the encounter in a primary antibody response
first disease encounter or first vaccination
38
What is the encounter in a secondary antibody response
second disease encounter or booster dose
39
What is the function of B-cells in adaptive immunity
- Differentiate into plasma cells that produce antibodies specific to the antigen - memory cells that retain the memory of the antigen for faster response on the second encounter
40
What type of adaptive immunity is involved in the B-cells
humoral
41
In B-cells, what is antigen bound
circulating blood
42
Are there sub-types of B-cells?
no
43
What is the function of T-cells in adaptive immunity
- Links the humoral and cell-mediated immunity - activates differentiation of B-cells to plasma and memory cells.
44
What type of adaptive immunity is involved with T-cells
Humoral and cell-mediated; both
45
In T-cells what is antigen bound
Present on MHC proteins on surface of APC or nucleated cell
46
Are their sub-types of T cells?
T helper cells T cytotoxic cells
47
What lymphocytes are involved in humoral immunity
B-cells to make antibodies specific for the antigen T helper cells assist
48
What antigens are recognized in humoral immunity
extracellular antigens that have been recognized by macrophages, phagocytosed, degraded, and antigens presented on the surface of APC only
49
What are the two mechanism levels in Humoral immunity
1. Clonal selection and expansion at the B-cells level 2. B-cell differentiation into plasma cells (antibody-producing cells) and memory cells for faster response on the second encounter. This step is influenced by T helper cells.
50
What is the host cell in humoral immunity
APC
51
What MHC is involved in humoral immunity
the antigen is presented on MHCII
52
What lymphocytes are involved in cell-mediated immunity
Cytotoxic T cells destroy the infected body cell
53
What levels of the mechanism are involved in cell-mediated immunity
Cytotoxic T cells recognize the antigen on surface of infected host cells
54
What is the antigen recognized in cell-mediated immunity
antigens are from intracellular pathogens like viruses and intracellular bacteria that did not enter the cell by phagocytosis
55
What is the host cell in cell-mediated immunity
any nucleated cell
56
What is the MHC involved in cell-mediated immunity
antigen presented on MHCI
57
What do Cytotoxic T cells secrete
1. Perforin 2. Toxic "Granzymes"
58
What do perforins do
forms pore in target cell membrane
59
What do toxic "granzymes" do
enter targe cell through pores and destroy it
60
What are the types of pathogens
Primary - disease in healthy host Opportunistic - disease in immunocompromised host
61
What are the types of pathogenicity
1. Infectivity - how easy is it for the pathogen to cause disease 2. Virulence - how severe is the disease
62
What are the virulence factors
1. pathogenicity islands 2. plasmids 3. phage genomes
63
What are the routes of transmission
1. Reservoir 2. Vector
64
An animal, bird, or insect that normally harbors the pathogen, in which the pathogen can replicate
reservoir
65
an insect or a tick that transmits the pathogen from one host or reservoir to the next
vector
66
What are the routes of transmission
- horizontally - vertical - accidental
67
transmission from one member of a species to another
horizontal transmission
68
the passage of a pathogen from parent to offspring
vertical transmission
69
when a host that is not part of the normal infection cycle unintentionally encounters that cycle. Usually, a reservoir is involved
accidental transmission
70
What are the portals of entry
1. oral with food 2. airborne 3. eye 4. mucosal surfaces 5. parenteral (injection in the bloodstream)
71
What are exotoxins?
- Gram-negative and positive species - synthesized in the cytoplasm; may or may not be secreted - protein, generally inactivated by heat - a distinct toxic mechanism for each - generally very potent; some are among the most potent toxins known
72
What are endotoxins
- gram-negative species only - component of the outer membrane - Lipopolysaccharide, heat stable - innate immune response; a systemic response leads to fever, a dramatic drop in blood pressure, and disseminated intravascular coagulation - not very toxic; small amounts lead to an appropriate response that helps clear an infection
73
What happens in the Type II secretion system for bacterial exotoxins
Ex: Cholera toxin Toxin secreted into periplasm first then moved out by a piston-like assembly
74
What happens in the Type III secretion system for bacterial exotoxins
Ex: Shiga toxin Toxin moves from cytoplasm directly to the outside (molecular syringe) without passing by periplasm
75
What happens in the Type IV secretion system for bacterial exotoxins
Ex: Bordetella pertussis Either could happen. toxin secreted or toxin moves
76
animal diseases accidentally transmitted to humans
Zoonotic disease
77
acquired in a hospital setting
nosocomial infections
78
The stimulation of an immune response by deliberate inoculation with an immunogen
immunization