3: L14 Flashcards

1
Q

what is inflammation characterised by

A
o	Swelling (tumor) 
o	Redness (rubor) 
o	Heat (calor) 
o	Pain (dolor)
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2
Q

What organs are immune privileged and what does that mean

A

o Developed own strategies to control
o Susceptable to tissue damage // cannot repair
o Immune response may actually damage structures resulting in loss of function

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3
Q

2 Types of immune suvrailence

A

Humoral + cellar

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4
Q

what are the two divisions of cellular immuntiy

A

innate + adoptive

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5
Q

Neutrophil Granulocytes & Macrophages function

A

take foreign particles and destroy them in lysosomes

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6
Q

Difference between neutrophil and macrophage

A

N= mobile, die after phagocytosis, 24hr life

M= months life, can engulf many pathogens, act as antigen presenting cells to T cells

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7
Q

Eosinophilic & Basophilic Granulocytes Mast cells , NK-cells function

A

deliver substances
kill parasites/tumur cells
induce or support inflammatory responses

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8
Q

function of M cells

A

• Transport antigens from lumen to lamina propria AG not normally allowed to cross lining

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9
Q

function of dendritic cells

A

• DCs Take up antigens from their environment

  • Activate phagocytic cells
  • Present antigens on MHC surface molecules to T-lymphocytes
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10
Q

follicular dendritic cells function

A

present antigen to B-lymphocytes

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11
Q

what are b lymphocytes also called

A

plasma cells

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12
Q

how are early b cells activated and their function

A

activated according to surface receptor (specific to AG) – = cells then “primed”
o Recognised with help of T cells and FDC they mature into plasma cells

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13
Q

plasma cell function

A

• Plasma cells: antibody production in lymphatic or migrate to other tissues
o Some ABs expressed on surface (eg IgA important in gut etc)
• Plasma cells make IgM / IgG

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14
Q

what do memory b cells do

A

react faster to same AG, mature cells, FDC not required activate

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15
Q

• Function of Antibodies

A

o Bind to antigenic (AG) molecules , Neutralize toxins
o Help phagocytosis, virus neutralisation
o Vaccines work by specific AB produced over long time

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16
Q

where is IgA, G and M distributed to

A
  • IgA - Added to secretion of glands , Tears , Nasal cavity , Bronchial surface , Gastrointestinal surface
  • IgG & IgM - Delivered to blood and extracellular liquid
  • Light chains + heavy chains (small/large connected by bonds)
17
Q

the production of antibodies is the main function of what system

A

humeral

18
Q

describe the ‘constant region;

A

Bottom of Y connects to cell surface (if antibody expressed on cell surface, this is what membrane binds tw), morphology more common to other antigens)
o Top arms of the Y= binds to antigen itself (each antigen= specific antigen site)

19
Q

what’s a light/heavy chain

A

on antibody- light chain is singular piece, heavy chain connect bottom of y to top

20
Q

Describe the primary AB response- first encounter antigen

A
  • B cells differentiate and activate- produces IgM (penta structure), + small amount of IgA (bc of 5 binding sites // mop up more antigen (despite being weaker immune response than IgG)
21
Q

Describe the secondary AB response- second encounter antigen

A

larger IgG response as stronger immune response

22
Q

describe why the antibody class switch from primary (M) to secondary (G)

A

o Within B cell germline, different parts of chromosome responsibly for particular parts
o V region (AB binding site)= V, D, J cites = splicing
• Different antibody combine DVJ in different sequences= permeablity + almost endless variation

23
Q

what are the two types of lymphocytes

A

Cytotoxic T-cells (CD8+)

Helper T-cells (CD4+)

24
Q

what do Cytotoxic T-cells (CD8+) do

A
  • Recognise foreign bodies – activated CTL
  • Kill virus infected cells
  • Kill tumour cells
25
Q

what do Helper T-cells (CD4+) do

A
  • Produce cytokines = hormone-like soluble factors
  • Regulate immune response through cell surface molecule interaction (cell:cell)
  • Regulate and Support B-cell differentiation (recognise same AG)
  • Recognise different parts of same AG (epitopes)
  • Support cytotoxic T-cell function (CD8+ must be activated (c.f. NK cells))
26
Q

describe the steps of Cytotoxic T-cells (CD8+)

A
  1. Infected cell= presentation of antigen molecule with CD8 marker + class 1 MHC (t cell recognises not normal cell + extra markers)
  2. Responds to these = production of active cytotoxic t cells
  3. = Produce lymphotoxin etc =designed to puncture and degrgade cell
    • Main driver= t cell receptor and CD8 molecule= complex created
27
Q

describe the steps of Helper T-cells (CD4+)

A
  1. Other cell degrade infected cell and presents antigens to T helper cells (presents Class II MHC co-localised with CD4)
  2. = activated + cell division > release cytosine
  3. Targets cell to destroy
  4. And memory cells primed and activated
28
Q

describe MHC protein role in ummuno

A

cell phagocytise pathogen/abnormal peptides and bind MHC to the unusual product (MHC Class II on the antigen presenting cell, and Class I on the peptides)

abnormal fragments displayed on membrane by MHC

29
Q

What does class 1 MHC activate

A

abnormal cell= CD8 T cells

Class II= presence of pathogen // CD4

30
Q

What are cytokines

A

Chemical messengers released by tissue cells:
• to coordinate local activities
• to act as hormones to affect whole body
Stimulate T cell divisions:

31
Q

difference between Th1 and 2 cytokines

A
TH1= Pro inflamm
Th2= antinflamm
32
Q

what do alpha, beta and gamma interferons do

A
  • Released by activated lymphocytes and macrophages (usually by virus)
  • Alpha interferons: produced by leukocytes stimulate NK cells
  • Beta interferons: secreted by fibroblasts slow inflammation
  • Gamma interferons: secreted by T cells and NK cells, stimulate macrophage activity