immunology Q&A Flashcards

1
Q

What invading enemies does the immune system have to fight against?

A

pathogens (invaders)

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2
Q

What are the main layers of the immune system?

A
  1. physical and chemical barriers
  2. non-specific innate immunity
  3. specific adaptive immunity
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3
Q

List three important discoveries that helped to identify the importance of the immune system and/or how “immunity” is obtained

A
  1. Edward Jenner observed milk-maids that contracted cowpox were resistant to smallpox
  2. Pasteur created the first vaccine (anti-rabies)
  3. The concept of humoral immunity was discovered in 1890 by Emil von Behring & who derived “antitoxins” from Tetanus
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4
Q

Describe the epithelial barrier.

A

The first line of defence, a physical & chemical barrier
one cell thick
separates microbe rich surface form body

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5
Q

What are the difference between innate and adaptive immune system?

A

innate = non specific immunity, includes first and second line of defense. slower
adaptive = specific immunity, includes t & b cells & antibodies. also dependant on previous exposure to pathogen. faster

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6
Q

-What is the most ancient immune response strategy?

A

the innate immune system

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7
Q

Define three main characteristics of HSCs (Hematopoietic Stem Cells)

A

1) all RBC and WBC develop from multipotent HSCs
2) is a rare cell type - self-renewing and multipotent
3) found mainly in bone marrow

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8
Q

What is the primary hematopoietic tissue?

A

bone marrow

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9
Q

-What are the cell types that originate from HSCs?

A

myeloid precursor & Lymphoid precursor

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10
Q

What are the differences between monocytes and macrophages?

A

macrophages are a differentiated monoctye
- increase in size, numbers, complexity, phagocytic activity, etc
- becomes a professional APC

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11
Q

What is the main difference between neutrophils and macrophages?

A

their lifespan.
neutrophils are short lived yet macrophages are long-lived

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12
Q

What is the main difference between dendritic cells and macrophages?

A

their role
macrophages = phagocytosis of microorganisms (innate effector cells)
DCs = stimulate T cell activation (induce adaptive immunity)

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13
Q

What is the main difference between Myeloid and Lymphoid cells?

A

the type of cell that they give rise to are all different

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14
Q

What are the analogies and differences between B cells and T cells?

A

-both lymphocytes
-B cells produce antibodies
-T cells destroy infected cells

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15
Q

What are the main/primary hematopoietic tissues in adult humans?

A

bone marrow & thymus

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16
Q

Why is the Thymus important?

A

it is the site of T and NKT cell maturation

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17
Q

What are the differences between the blood and the lymphatic System?

A

lymphatic system = drains lymph fluid from extravascular tissues, from capillaries through lymphatic vessel - lymph node - thoracic duct - back into bloodstream
blood system = pumps blood throughout the body

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18
Q

What are the main lymphoid tissues?

A

primary: thymus and bone marrow
secondary: lymph nodes, spleen, MALT (mucosal-associated lymphoid tissues)
tertiary: CALT (cutaneous-associated lymphoid tissue)

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19
Q

List the main lymphoid secondary tissues and describe their structures and functions.

A

lymph node: site of generation of T cell response and B cell antibody response to specific antigen
spleen: where immune responses are mounted against antigens in the blood
overall: this is where the antigen is trapped

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20
Q

How do immune cells communicate with each other and with other body cells?

A

through cytokines

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21
Q

What are cytokines

A

proteins that communicate among cells of immune system

22
Q

What are chemokines?

A

cytokines that attract cells with the appropriate receptors to regions where the chemokine concentration is the highest

23
Q

In how many ways can cytokines work?

A

3 ways: endocrine, paracrine, and autocrine action

24
Q

How many classes of Ig are in vertebrates?

A

5:
IgG, IgM, IgA, IgE, IgD

25
Q

What mechanisms ensure the high diversity in Ig?

A

Somatic hypermutation, somatic recombination, class switch

26
Q

How many different antibodies can be generated based only on the mechanisms of genomic recombination and class switch?

A

about 10^18 different antibodies

27
Q

What is the complement?

A

set of circulating, inactive proteins that are activated in response to a pathogen

28
Q

How many route of activation of the complement have been described?

A

3, classical, mannose-binding lectin mediated and alternative

29
Q

what is inflammation?

A

a non-specific reaction to noxious stimuli

30
Q

How is an inflammatory process generated, and what are the consequences of inflammation?

A

generated by redness, swelling, pain and heat localized at site of infection
consequences: damage to healthy tissue in lungs and brain tissue

31
Q

Define PAMPs and PRRs.

A

PAMP: pathogen-associated molecular pattern
PRR: patten recognition receptors

32
Q

What are the known differences between innate and adaptive immune recognition of pathogens?

A

innate: non -specific, not directed against specific pathogen
adaptive: recognizes and destroys based off memory

33
Q

What are the different TLRs, and what do they recognize?

A

TLR: Toll like receptor
they recognize PAMPS

34
Q

How do the PRR signal transduction pathways work?

A

-PRR recognizes a PAMP, and sends signal to the nucleus
-signal activates transcription factors to turn on genes

35
Q

What happens after APC cells engulf a pathogen or are activated upon PRR-PAMP interaction?

A

phagocytose the microbes

36
Q

Where are T-cells activated?

A

lymph nodes
(on the surface of APC like DC)

37
Q

-Describe the T-cells activation process

A

APC activated by PRR and makes IL-12
costimulation B7-CD28
results in activation and signal transduction -> IL-2 & IL-2R

38
Q

Where are B-cells activated?

A

in the lymph node

39
Q

How are B-cells activated?

A

co-stimulation via cell surface ligand-receptor pairs and additional help vis cytokines (IL-4) activates b cell
the b cell - t cell interaction

40
Q

What is the consequence of B-cells activation?

A

their activity in the germinal center
they undergo clonal expansion

41
Q

How T cells encounter antigen in the lymph node and get activated

A

the CD4 binds to class II MHC, the APC activated by PRR will make IL-12, and with costimulation the t cell is activated

42
Q

How B cells encounter antigen in the lymph node and become plasma cells

A

the t cell - b cell interaction
activated b cell proliferates and clones become memory or plasma cells

43
Q

Describe how interferon is made and protects against viral infection

A

produced by virally infected cells
- they serve as a warning system & prevent viral replication

44
Q

What are NK cells and where do they originate?

A

cytotoxic lymphocytes and they originate in the bone marrow as an HSC

45
Q

Describe the main characteristic of the NK cells receptor

A

they express a set of activating and inhibiting receptors, these receptors are used to determine whether or not to kill a target cell or not

46
Q

How do NK cells kill the viruses?

A

inducing apoptosis by the release of perforins/granzymes at the junction of the two cells

47
Q

What types of peptides are presented by MHC-I?

A

Present endogenous & foreign cytosolic antigens on MHC I to CD* T cells

48
Q

What are the two ways CTL kill target cells?

A
  1. Perforin/gramzyme pathways
  2. Fas/FasL pathways
49
Q

How are NK cells regulated by inhibitory and activating receptors?

A

if a cell lacks MHC I and displays a stress protein, an NK cell will activate to destroy the target

50
Q

Describe the strategy for the diversity of MHC-Iand receptors in the human population and why it exists

A

-there is such a diversity in MHC molecules b/c of how fast pathogens evolve
-strategy= high polymorphism

51
Q

How antibodies block viral infections (antibodies protection)

A
  1. block attachement
  2. aggregate for phagocytosis
  3. activate complement for MAC attack