How do we eliminate pathogens that live outside cells Flashcards

1
Q

what are the primary lymphoid organs

A

thymus and bone marrow, where immune cells are made

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2
Q

what are the secondary lymphoid organs

A

where immune systems happen, these include all the lymph nodes, spleen and lots of lymphoid tissue such as payers patches in the gut, T and B cell conduct immune response in this tissue(adaptive response)

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3
Q

what do people have

A

different number of lymphoid tissues

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4
Q

describe how draining lymph nodes work

A
  • Draining lymph nodes drain areas where they are near,
  • The blood comes out of the circulation system with nutrient and oxygen in it and the liquid has to get back into the blood so it comes back down the lymphatic vessel through the lymph node then back to the thoracic duct. This acts as a drain as it drains the tissue, therefore anything that is infected goes to the lymph node
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5
Q

what does the spleen do

A
  • Spleen does this from the blood, it cleans the blood, therefore if you don’t have spleen you are vulnerable to blood diseases
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6
Q

what stays in the secondary lymphoid for a long time

A
  • T and B cell can stay in secondary lymphoid number for a long time without being used they are only activated when you have an infection which they detect from the tissue
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7
Q

describe the basis of the immune response

A
  • If you cut yourself PRR receptors on the cells of the innate immune system (such as macrophages) recognise the pathogens around and this causes inflammation and the innate immune response can keep the level of pathogens down and occasionally get rid of the pathogen on its own
  • The inflammation gets a lot of fluid in the area and this allows more liquid to come out and forces liquid down the lymph nodes, this forces bits and pieces of pathogens to go down there and cells to go into the lymph nodes such as dendritic cells
  • Dendritic cells crawl around the tissues and detect pathogens and pick up pieces of dead cell this causes them to become activated and mature so they no longer crawl around and they chop bits of protein up putting them on MHC class I and class II
  • They go to the lymph node
  • Try to find b and t cells that recognise these pathogens
  • T and B cells that recognise the pathogens clonally expand
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8
Q

what does the Body use to get rid of extracellular pathogens

A
  • Use things in the body fluid to get rid of the pathogens such as
  • antibodies
  • complement proteins,
  • phagocytosis
  • antibodies
  • antimicrobial peptides
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9
Q

what are the extracellular spaces in the immune response

A
  • blood
  • lymph
  • interstitial spaces
  • epithelial surfaces
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10
Q

what are the intracellular cell surfaces in the immune response

A

cytoplasmic and vesicular

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11
Q

what are the cells that respond to the intracellular infection

A

– cytotoxic T cells,

  • NK cells,
  • T cell dependent macrophage activation are involved in killing the cell
  • Once pathogen is in the cell than it is killed or it has something squirted at it is not repaired – stops the spread of the disease
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12
Q

what is the humeral immune response

A

this is the immune response associated with body fluids

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13
Q

what are the body humors

A

these are the body fluids

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14
Q

what do B cells do to works

A

B cells make antibodies

- Antibodies stick to antigens – irritates the worm so much that it leaves

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15
Q

describe the antibody structure

A
  • Heavy chain has different types which leads to the different isotypes
  • Only make 5 different types of antibodies
  • FAB end bind to the antigens (variable region) -
  • FC end bind to the heavy chain (constant region) – FC – fragment of crystalisation
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16
Q

what are the two ends of the antibody

A
  • FAB end bind to the antigens (variable region) -

- FC end bind to the heavy chain (constant region) – FC – fragment of crystalisation

17
Q

what are the heavy chain isotopes

A
U = Igm
Circle with pony tail = IgD
Gamma = IgG 
Alpha – IgA
Funny E – IgE
18
Q

what does the FC portion of the heavy chain do

A

the FC portion of the heavy chain dictates the function of the antibody such as is it secreted in the lungs, does it form a dimer

19
Q

what is the structure of the antibody isotopes

A

IgD, IgE, IgG – monomer
IgA – dimer
Pentamer – IgM

20
Q

what are the monomer antibody isotopes

A

IgD, IgE, IgG

21
Q

what are the dimer antibody isotopes

A

IgA

22
Q

what are the pentamer isotopes

A

IgM

23
Q

How many different antibodies are there

A

375 million

24
Q

What are the 5 basic things that antibodies need to do

A
  • Neutralisation – prevent it entering cells
  • Opsonisation - macrophages recognise the FC end of the antibody and when it sees a lot of FC it can eat it
  • Agglutination – easier to deal with by cells – sticked together
  • Antibody-dependent cell killing ADCC (by NK cells) – the FC portion of the antibody is reconised and then the NK kills the cell by squirting things at it
  • Activation of complement – classical pathway
25
Q

POINTS TO REMEMBER

A
  • each B cell makes a supply of a unique antibody
  • each antibody recognises a different antigen
  • we make millions of B cells
  • SO we make millions of different antibodies
26
Q

IgA

A
  • secrete grams of IgA into the gut

- every bacteria in the gut is covered in IgA

27
Q

IgM

A
  • forms clumps and sticks things together

- first antibody that the plasma cell makes

28
Q

How does B cell activation happen

A
  • Resting B cell,
  • Antigen binds to B cell
  • Activates B cell
  • Activated T cell which help the activated B cells
  • Form the plasma cell, for IgM
  • Or form IgG, IgA, IgE
29
Q

How does the complements cascade work

A
  • Proteins are activated in the blood and when they see bacterium and when they see antibodies bound to bacterium they become activated and form a complex that leads to the formation of the pore which pops the bacterium
  • Our cells have proteins on the surface which inactivate the complement proteins
30
Q

what are super antibodies

A
  • made next time that you are infected by for example influenza
  • specials cells that take bits and pieces of influenza and hold it out to B cells that have already been activated by influenza, int he germinal centres they start to mutation the ends of the Y molecule so the FAB areas
  • makes a few modifications and makes a better fit to the antigen
  • if it is a better fit then it is given a growth factor and starts dividing producing daughter cells
  • this happens in the germinal centres in lymph nodes and spleen
31
Q

what organisms invade outside of cells

A
Extracellular bacteria: 
Staph. Aures
Staph. Pyogenes 
Bordetella Pertussus
E. coli

Fungi

Helminths

32
Q

what are exotoxins

A

a toxin release by a living bacterial cell into its surroundings (eg Cholera)

33
Q

what are endotoxin

A

Lipopolysaccharide molecules associated with the outer membrane of gram negative bacteria (eg Neisseria Meningitidis)

34
Q

what are the components that make up the humeral immune response

A

B cells/Plasma cells

T helper cells

(macrophages)

35
Q

How does the humeral immune response work

A

step 1; the periphery

  • Bacteria are engulfed by macrophages, the macrophages then display the surface antigens of the bacteria using MHC class II, it is now an antigen presenting cell (APC)
  • T helper cells recognize the antigen displayed by the APC using T cell receptors, the APC then secretes Interleukin I
  • The Th cell then produces interleukin II, which triggers T cell proliferation and formation of antigen specific receptors – it is an activated T cell

Step 2 lymph nodes

  • B cells engulf the bacteria and display the surface anigens using MHC class II – it is now an APC
  • Circulating activated T cells can now recognize the B cells using their antigen specific receptors
  • The activated T cells dock with the B cells and releases cytokines that trigger B cell proliferation and differentiation into plasma cells
  • The plasma cells can now secrete antibodies that are specific to the invading pathogen
36
Q

what is an antibody

A

Antibodies are glycoproteins produced in response to invading foreign particles

37
Q

what I need to know for the complement pathway

A

Complement proteins are a number of serum plasma proteins that circulate around the body
The C1 complement protein is activated by the antigen-antibody complex
This triggers the activation of the other complement proteins which trigger inflammation, opsonize bacteria and form the “membrane attack complex” (MAC)