Immunity Flashcards

(40 cards)

0
Q

What is the role of transferrin and lactoferrin, and where can they be found?

A

Sequesters iron; found in saliva, mucus, milk, blood, and extracellular fluid

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1
Q

What is the role of lysozyme, and where can it be found?

A

Degrades peptidoglycan; found in tears, saliva, mucus, phagocytic cells, blood, extracellular fluid

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2
Q

What is the role of anti-microbial peptides (AMPs)?

A

Disrupt integrity of bacterial cells by forming pores; found in mucous membranes and within phagocytic cells

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3
Q

Define: pathogenicity

A

The ability of an organism to cause disease

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4
Q

Define: virulence

A

How pathogenic an organism is

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5
Q

How are invaders detected by the immune system?

A

Toll-like receptors (TLRs) bind to pathogen-associated molecular patterns (PAMPs)

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6
Q

What are a few types of PAMPs?

A

Flagellin, peptidoglycan, LPS, dsRNA, unmethylated DNA

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7
Q

Which immune cells are phagocytes?

A

Macrophages, mast cells, neutrophils, and dendritic cells

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8
Q

Which of the phagocytes can kill bacteria extracellularly, and how do they do this?

A

Neutrophils; they release web-like genetic material

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9
Q

What is the role of antigen-presenting cells?

A

They display digested microbial antigens on their surface and activate T-helper cells

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10
Q

In the complement system, what is the role of C3b?

A

It activates C5, splitting it into C5a and C5b. It also binds to foreign material (opsonization) to make phagocytosis easier.

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11
Q

What is the role of C5a?

A

It acts as a powerful phagocyte chemoattractant. Together with C3a it also increases vascular permeability

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12
Q

What is the role of C5b?

A

Togther with C6, C7, C8, and C9 it forms transmembrane channels in invaders (Membrane-attack complex MAC).

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13
Q

How are natural killer cells inhibited?

A

Killer Inhibitor Receptors recognic class I MHC molecules on a cell surface

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14
Q

What type of molecules are highly antigenic?

A

Proteins and polysaccharides

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15
Q

What type of molecules are poorly antigenic?

A

Lipids and nucleic acids

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16
Q

Which Ig is produced first during the primary response?

17
Q

Which Ig circulates as a pentamer?

18
Q

Which Ig is most abundant in blood and tissue fluids?

19
Q

Which Ig provides the longest-term protection?

20
Q

Which Ig is primary during the secondary response?

21
Q

Which Ig is most abundantly produced?

22
Q

Which Ig serves as B cell receptor?

23
Q

Which Ig is active against helminths and other parasites?

24
Where do B-lymphocytes mature?
In the bone marrow
25
Where do naive B-lymphocytes reside?
Lymphoid organs and tissues
26
What three gene segments are joined together during B cell maturation?
V, D, and J
27
What two events must occur in order for a B cell to activate?
An antigen must bind a B-cell receptor, and helper T cells must confirm
28
Where do memory B cells reside?
Bone marrow, lymph nodes, spleen
29
What do helper T cells do, once activated?
Release cytokines and help activate B cells, macrophages, and cytotoxic T cells
30
What is Type I hypersensitivity?
Anaphylactic--IgE triggers release of cytokines by mast cells
31
What is the idea behind desensitization in Type I hypersensitivity?
Extremely dilute solutions of antigen might cause IgG to be produced instead of IgE, reducing the reaction
32
What is Type II hypersensitivity?
Cytotoxic
33
What mediates Type II hypersensitivity, and what disease is an example?
Antibody-activated complement; hemolytic disease of newborns
34
What is Type III hypersensitivity?
Complex-mediated
35
Describe Type III hypersensitivity
Slight excess of antigen over antibody can cause Ag-Ig complexes to deposit in blood vessels and tissues; complement activates and leads to inflammatory events
36
What is Type IV hypersensitivity?
Delayed cell-mediated
37
What causes Type IV hypersensitivity?
T cells; first contact with a hapten primes your immune system to overreact to subsequent reactions
38
What type of hypersensitivity is responsible for most types of contact dermatitis and organ rejection?
Type IV (delayed cell-mediated)
39
In severe combined immunodeficiency, two different types of mutations occur. What types are they and what do they cause?
An X-linked recessive mutation causes lack of communication between B and T cells; an autosomal recessive mutation cause accumulation of deoxyadenosine, which is toxic to B and T cells.