Recognition of Antigen by the Adaptive Immune System NOT FINISHED Flashcards

1
Q

Define antigens

A

Molecules that induce an immune response through the activation of antigen specific lymphocytes

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2
Q

What are the 3 groups of molecules that work together to recognise antigen for the adaptive immune system?

A
  1. Major histocompatability complex (MHC)
  2. B cell receptors
  3. T cell receptors
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3
Q

What is the first response of a B/T cell when it encounters an antigen, that its receptor is specific for? Why?

A

They expand in number.
To increase number of cells able to respond to pathogen
Lymphocytes persist post-infection –> memory

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4
Q

There are a huge range of antigens, therefore B and T cells have to be very diverse. How do they achieve this?

A
  • gene rearrangement of the different parts encoding the receptor (combinatorial diversity)
  • B cell receptors achieve diversity and further specificity for antigen through a process of rapid mutation called hypermutation
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5
Q

What is the different between peptides that B cells and T cells are able to recognise? How do they overcome this?

A
  • T cells can only recognise short peptide sequences from antigens. The pathogen must be broken down and processed into smaller peptides within an antigen presenting cell and then present on their surface by a presenting molecule such as MHC
  • B cells can recognise while antigen through their B cell receptor which binds to surface molecules or patterns. Soluble antigen receptors (antibodies/immunoglobulin) are then released from terminally differentiated B cells. Antibodies are then very effective at presenting antigen to T cells
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6
Q

What is the simple difference between major histocompatabiity complex class 1 and 2?

A

Class I recognises peptides derived from endogenous proteins
Class II recognises peptides processed from exogenous proteins

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7
Q

Where are Class I MHC molecules found?

A

on all nucleated cells, except neurones

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8
Q

What two things do MHC class I molecules allow the recognition of?

A

infected cells i.e. by viruses

abnormal changes occurring in a cell i.e. cancer

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9
Q

What is proteolytic activity?

How does this relate to MHC activity?

A
The continuous process by which the cells of the body break down a proportion of the proteins they are producing. 
Most amino acids are recycled but some are transported through ER to surface and loaded onto the peptide-binding groove of a class 1 MHC molecule.
--> viral proteins are expressed on the cells surface
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10
Q

How is the MHC Class I: peptide complex recognised and what is the result of this?

A

Recognised by cytotoxic T cell specific for that viral peptide
Cytotoxic T-cells express CD8 (coreceptor for TCR).
CD8 facilitates interaction between T cell and MHC Class I on infected cell.
Triggers cytotoxic T cell to kill the virally infected cell by inducing apoptosis.
The cell is then consumed by macrophages

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11
Q

What are the rolls of the following in MHC Class I mechanism of working?

  1. TAP protein
  2. calnexin and calreticulin
  3. Tapasin
A
  1. TAP protein controls the movement of viral proteins into the ER
  2. Calnexin and calreticulin assists in the folding of MHC. These are needed because the protein is relatively unstable before it has bound peptide.
  3. A pool of MHC is retained in the ER by the protein Tapasin, so that a rapid increase in surface peptide/MHC complexes can occur following peptide binding
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12
Q

Which cells express MHC II?

A

antigen presenting cells

e.g. dendritic cells, monocytes/macrophages and B cells

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13
Q

How is MHC II protected from picking up antigen before it reaches the ER?

A
  • complexed with a protein called the invariant chain

- degraded in the ER and epitope is inserted

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14
Q

Which cells do MHC II present antigen to?

A

CD4 T cells

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15
Q

How does CD4 interact with MHC II. What events follow this interaction?

A

T helper cells express CD4 as well as TCR’s. When CD4 interacts with MHC II its TCR can meet and become specific for the antigen being presented.
Depending on cytokine environment, T cell polarises to become a memory cell of effete cell (Th1, Th2 and T regulatory and Th17 cells

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16
Q

What is mean by the term histocompatibility?

A

describes tissue that is compatible on transplantation

need to match MHC molecules to prevent immune activation and rejection

17
Q

What are the 2 sites of B cell development?

A

within the bone marrow and then in secondary lymphoid orange when they encounter antigen

  • for maturing B cells, their unique antibody is used a their membrane receipt for antigen.
  • antigen experienced B cells (plasma cells) sed their immunoglobulin and secrete it to become effector molecules
18
Q

What is the basic structure of immunoglobulin?

A

pair of identical heavy chains - connective by a disulphide bond
pair of identical light chains - connected to heavy chain by disulphide bond

19
Q

What molecule is often used identify B cells?

A

CD19

20
Q

How do the different parts of immunoglobulin differ in function?

A

Hypervariable/complementary determining regions = bind antigen
Constant domains = kappa/lamba, IgM/IgG/IgG/IgE/IgA
= determines function

21
Q

Describe the structure of the T cell receptor

A
  • two non-identical Ig-domain polypeptide chains
  • can be alpha and beta
  • or gamma and delta
  • same as BCR in that it has a short cytoplasmic tail –> reliant on a collection of accessory signalling molecules, the CD3 complex
22
Q

What is the name of the mechanism evolved to combat pathogen diversity

A

somatic recombination - this happens in the absence of antibody

23
Q

The genes that encode for variable regions are composed of different segments.
What are these segments?
What is their significance?

A
variable domain V
diversity D
joining J
constant C
Each segment represented many times, each varying slightly from the next. By randomly combining gene segments, unique and highly variable domain structures can form.
24
Q

Which two enzymes are required to rearrange genes in a specify order?

A

recombinase activating genes

RAG 1 and RAG 2

25
Q

What are the clinical effects of a lack of RAG enzymes?

A

B nor T cells develop and infants suffered severe threatening infections due to a condition call Severe Combined Immunodeficiency Disease SCID