Lecture 13 Flashcards

1
Q

List the 4 factors the establishment of an infection depends on.

A

Characteristics of the microorganism, number of organisms, mode of transmission, stability of organism

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2
Q

Almost all infections begin at an _____________.

A

epithelial surface

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3
Q

When does adaptive immune response become important?

A

When innate immunity can’t deal with the infection within a couple of day.

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4
Q

List the 5 major classes of pathogens?

A

Viruses, bacteria, fungi, protozoa, worms

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5
Q

Cytokines made in the later stages of an infection influence differentiation of ________ toward ___ or ____ cells.

A

CD4 T cells; TH1; TH2

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6
Q

Pathogens influence cytokines that affect ___ differentiation into ___or ___.

A

TH0; TH1; TH2

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7
Q

The distinct subset of ______ cell can regulate each other’s regulation.

A

CD4 T

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8
Q

IL-10 from TH2 causes __________ of TH1 development by suppressing ____ production by DC.

A

inhibition; IL-12

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9
Q

IFN-gamma from TH1 causes inhibition of ___ development

A

TH2

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10
Q

T cell subset produce __________ that regulate the development of other subsets. For ex. ___ (1.) inhibits ____ (2.) and vice versa. So, most responses are dominated by either ___ (1.) or ____ (2.) and are not __________ responses.

A

cytokines; TH1; TH2; balanced

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11
Q

To initiate extravasation, most of the antigen-specific T cells cease production of ___________ and express ______, which binds to ______ that is induced on activated endothelial cells.

A

L-selectin; VLA-4; VCAM-1

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12
Q

In the absence of a previous inflammatory response, activated T cell enter all tissues via _________: ________ interaction.

A

P-selectin; PSGL-1

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13
Q

Effector T cells that recognize pathogen antigens in tissue:
Produce…
Activate… (2)
Express…
Action on…

A

cytokines
endothelial cells and adhesion molecules on T cells
E-selectin, VCAM
effector T cells

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14
Q

Effector T cells change their adhesion molecules so they can migrate to the site of an __________. So, adhesion molecules _________ trafficking.

A

Infection; regulate

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15
Q

______________ organs are the site of antigen-specific B cell activation.

A

Peripheral lymphoid

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16
Q

What is protective immunity?

A

The resistance to a pathogen that results from infection or vaccination.

17
Q

Immunological memory is __________ after infection or vaccination. It needs to be maintain be repeated exposure to infectious virus. The memory response had an approximate half-life of between __ to __ years.

A

long-lived; 8; 15

18
Q

Antigen-specific memory B cells differ both quantatively and qualitatively from ________ cells.

B cell frequency : ___ fold increase.

Antibody affinity : ______ (higher/lower)

Isotypes : __, __, __

A

naïve B; 100; higher; Ig G,A,E

19
Q

Affinity maturation is a form of ____________ (somatic evolution) where B cells, using their surface antibodies (____), compete for limiting amounts of antigen. The B cell compete with each other and with free antibody produced by ___________. The B cells with the highest __________ will be able to bind to ______ and remain __________.

A

somatic selection; BCRs; plasma cells/plasmablasts; binding affinity; antigen; activated

20
Q

Long-lived Memory B cells have high _________ and high levels of ___ so they are efficient at acquiring _______ (signal 1) and ready to get ______ (signal 2)

Memory B cells have ___ on their surface so they can activate or participate in activation of ___ (memory) cells.

A

affinity antibody; MHC; antigens; T help

B7; TH2

21
Q

Naive T cells require contact with ____________ and the cytokines ___ and ____ for survival. Most activated T cells become effector T cells and are short-lived and die by __________. Or some are activated effector cells become long-lived memory cells that need cytokines ____ and ____ for survival.

A

MHC self peptides; IL-7; IL-15; apoptosis; IL-7; IL-15

22
Q

Memory T cells need ___________ to proliferate.

A

MHC self peptide

23
Q

Naive B cells either become _________ which eventually dies by ________ or become ___________.

A

plasma cells; apoptosis; memory B cells

24
Q

When antigens have both epitopes that were “seen” before and new epitopes, the memory responses to the epitopes seen before will _______ and there may be no ________ for new epitopes.

A

dominate; responses

25
Q

How do infectious organisms cause disease?

A

By evading the body’s initial immune defenses and triggering an adaptive immune response. When a pathogen breaches physical barriers, the adaptive immune system responds by recognizing and targeting specific antigens on the pathogen. During this process, B and T cells are activated to produce antibodies and cytotoxic cells that neutralize or destroy the invaders. Following the resolution of infection, most effector cells die, but memory cells remain, providing long-term immunity and a faster, more efficient response if the same pathogen is encountered again.

26
Q

What is the result of an immune response?(4)

A

There are no pathogens remaining.
Sometimes, the infection is contained but not eliminated.
Sometimes the pathogen or immune response (or both) leave significant tissue damage.
Often long-life journey.

27
Q

What governs whether a Th0 differentiates into TH1 or TH2?

A

Pathogens influence the cytokines.

28
Q

Differential expression of adhesion molecules can direct what?

A

Different subsets of effector T cells to specific sites: the selective expression of different homing receptors that bind to tissue-specific addressins (P-selectin)

29
Q

What is affinity maturation?

A

A form of somatic selection where B cells compete for limiting amounts of antigen to bind to and remain activated.

30
Q

What 2 components does protective immunity consist of?

A

Preformed immune reactants : Abs, effector T cells
Long-lived immunological memory

31
Q

Give a way CD8 cells that can be activated in the absence of CD4 cells.

A

Activated by dendritic cells.