Final exam Flashcards

(41 cards)

1
Q

MCSF function

A

Promotes monocyte differentiation into macrophage

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2
Q

Why don’t macrophages undergo diapedesis?

A

Because they reside extravascular

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3
Q

Macrophage size

A

80-100 microns

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4
Q

Motility definition

A

Ability to move spontaneously by expanding energy

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5
Q

Define phagocytes

A

Cells that protect a body by ingesting foreign objects

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6
Q

Clonal selection theory

A

Clonal selection theory explains how adaptive immunity works, stating that lymphocytes specific to an antigen are selectively activated and proliferate upon encountering that antigen.

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7
Q

2 subtypes of acquired immunity

A

Humoral
Cell mediated

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8
Q

(T/F) NK cells require stressed cells to display MHC or Ab

A

False

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9
Q

TH1 is for humoral/cell mediated

A

Cell mediated

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10
Q

TH2 is for humoral/cell mediated

A

Humoral immunity

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11
Q

MHC classes

A

MHC only displays peptides

Class 1: Intracellular source
Class 2: Extracellular source

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12
Q

Two ways antibody contribute to immunity

A
  1. Activation of complement system
    - leads to pathogen lysis
  2. Opsonization
    - leads to phagocytosis
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13
Q

4 main steps in wound healing

A
  1. Injury
    - few mins
  2. Coagulation
    - few hours
  3. Inflammation
    - few hours
  4. Repair and remodeling
    - weeks ~ months
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14
Q

Describe the difference between angiogenesis and vasculogenesis

A

Angiogenesis:
* Formation of new blood vessels from pre-existing ones.
* Occurs during wound healing, tumor growth, and tissue repair.
* Involves sprouting, proliferation, migration, and remodeling of endothelial cells.

Vasculogenesis:
* De novo formation of blood vessels from precursor cells.
* Occurs during embryonic development.
* Involves differentiation of angioblasts into endothelial cells and their assembly into primitive vascular structures.

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15
Q

Granulation tissue

A
  • type of connective tissue
  • scar tissue in early wound healing
  • subset of fibrosis
  • highly vascular, red, bumpy tissue, often moist, bleeds easily
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16
Q

When does remodeling phase begin

A

When production and degradation of fibrosis collagen is equal

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17
Q

What happens during remodeling phase

A

Disorganized collagen is rearranged and cross-linked in the direction of load bearing axis (tension or compression)

18
Q

Why is blood important during remodeling phase

A

They deliver nutrients and oxygen (angiogenesis!)

19
Q

Describe the timing aspects of wound healing

A
  1. Blood clotting (immediate)
  2. Clot break down (1-2 days)
  3. Appearance of granulation tissue with angiogenesis (3-5 days)
  4. Proliferative/repair phase (several weeks)
  5. Remodeling phase (several years)
20
Q

What can arrest wound healing process in the inflammatory stage?

How does this do so?

A

Chronic inflammation

  • This can lead to impaired matrix formation
  • Inadequate or inactive GFs
  • Mis-regulated enzymes
21
Q

How does infection lead to risk of chronic non-healing?

A

Prolonged inflammatory phase reduces ability of the tissue to proliferate

22
Q

Surface analytical techniques generate information about the (3 things)

A
  • topography
  • chemical composition
  • interaction
23
Q

Should we include efficacy with safety?

A

No! Lychees can be effective, but not safe!

24
Q

What is meant by safety?

A

Non-injurious
Non-toxic

25
Are biocompatibility and bioactivity the same
No. Bioactivity refers to eliciting a specific response at the surface of the material. For example, contact lenses are not bioactive. However, all materials that interacts with the body must be biocompatible.
26
Most pre-clinical testing is done on _____ instead of the ______
Material, whole device
27
3 classes of medical devices
Class 1 - does not sustain human life, been around a while - most exempt from 510k clearance Class 2 - most require 510k clearance Class 3 - supports or sustains life - nearly all require premarket approval (PMA)
28
What is 510k
Premarket submission made to FDA that the medical device is substantially equivalent to the one that exists in the market (=predicate device), that does not require PMA
29
Sequence of tests
1. In vitro 2. Ex vivo 3. Animal models (sheeps, pigs) 4. Clinical trials
30
Purpose of in vitro testing
Used to screen materials and devices for BIOCOMPATIBILITY
31
Cost for in vitro testing
100s~ 1000s
32
Cost for in vitro lab facility
50k ~ 100k
33
Which state of testing involves relatively fast processing of a large number of materials and prototypes?
In vitro testing
34
Limitations of in vitro testing
No understanding of efficacy (just know the material does not kill cells) No understanding of systemic toxicity, only at the individual cell level
35
Purpose of in vitro study
Used to screen materials and devices for biocompatibility
36
What is the size progression of animal models
Small -> large Generally, larger animals are mroe expensive.
37
What does every school + industry have that evaluates animal care and use program?
IACUC
38
Things to consider when using animal mdoels
* must choose appropriate species + justify it * carefully plan experiments using smallest number of animals that will use statistical result * animal welfare act of 1966 - addresses care + use of lab animals
39
5 essential features of clinical trials
1. uses defined inclusion/exclusion rules - age/weight requirements 2. use of control groups 3. subjects assigned to groups randomly 4. double-blinded studies 5. adequate size of experimental/control groups
40
Cost of non-human primates
millions
41