6. Adaptive immune response Flashcards

1
Q

What are naive T cells?

A

T cells that has not encountered an antigen

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2
Q

Which cell is required for naive T cells to be activated?

A
Antigen presenting cells.
These APCs:
Sense the pathogen
Capture the pathogen
Process the pathogen
Present their antigens on their surface.
The naive T cells will bind to the APCs and will be activated
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3
Q

Differentiate between naive T cells and effector T cells

A

Naïve T cells = T cells that have not previously encountered the antigen

Effector T cells = T cells that have previously encountered the antigen and are capable of performing effector functions during an immune response

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4
Q

List the 4 main types of APCs and provide the type of cell they provide the pathogen to as well as the function of the activated T cell

A
  1. Dendritic cells
    They present the pathogen to naive T cells.
    The T cell mounts a response against most pathogens.
  2. Langerhans cells
    They present the pathogen to naive T cells.
    The T cell mounts a response against most pathogens.
  3. Macrophages
    They present the pathogen to effector T cells.
    The T cells are used to stimulate and increase the activity of phagocytes in destroying pathogens.
  4. B cells
    They present the pathogen to effector T cells.
    The T cells are used to stimulate and increase the antibody response (humoral response).
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5
Q

Give the 3 main features of APCs

A
  1. These APCs have strategic positioning within the body and can be found at every portal of entry.
    E.g
    o Mucosal membranes(MALT) (gut(GALT), lung)(NALT, BALT, GUALT)
    o Skin (i.e., Langerhans cells) (SALT)
    o Blood (i.e., plasmacytoid cells)
    o Lymph nodes (i.e., follicular dendritic cells)
    o Spleen
  2. There’s diversity when it comes to the pathogen sensors (PRRs) found in these APCs.
    There’ll be different types of PRRs for extracellular as well as intracellular pathogens(virus).
  3. There’s diversity in the mechanisms used to capture pathogens.
    E.g phagocytosis in order to capture the whole microbe whilst macropinocytosis is used to capture soluble particles.
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6
Q

Best type of PRR? Why is it important?

A

Toll like receptor

Over activation of TLR4 in sepsis leading to organ failure.

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7
Q

Why are antigen presenting cells important?

A

Only way to activate T cells to stimulate immune response.

Tells T cell that’s there’s an invader
What the invader looks like
What response T cell needs to do

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8
Q

Why do we struggle to ID cancer?

A

Some cancers can emit signals that can suppress immune system.

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9
Q

Describe the steps taken when a pathogen enters the body

A
  1. There’s a breach in the innate barriers somewhere in the body allowing the pathogen to enter the body.
  2. Macrophages of the innate immunity start triggering the innate immune process.
  3. If the microbe gets into the blood it’ll end up reaching the spleen where’ll it be captured.
  4. Antigen presenting cells will pick up the pathogens in tissue and use the lymphatics to capture it.
    They’ll then take it to the nearest lymphoid tissue (e.g the BALT) where there’s an abundance of adaptive immune cells.
  5. The pathogen is processed and there’s the expression of microbial antigens on APCs.
  6. The microbial antigen is then presented to the right T cells.
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10
Q

What is an HLA system?

A

The human leukocyte antigen (HLA) system or complex is a gene complex that codes for the major histocompatibility complex (MHC) proteins in humans.
HLA genes are highly polymorphic, which means that they have many different alleles, allowing them to fine-tune the adaptive immune system.

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11
Q

How are pathogens presented on the surface of an APC, differentiate between the 2 molecules involved

A

Pathogens are presented by Major Histocompatibility Complex (MHC) molecules.

There are 2 types:

  1. The MHC class 2 molecules
  2. MHC class 1 molecules
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12
Q

Where are antigen presenting cells found?

A

o Mucosa associated lymphoid tissue (MALT)

  • Skin (SALT)
  • Mucous membranes (GALT, NALT, BALT, GUALT)
  • Tonsils or Peyer’s patches

o Lymphoid organs (Lymph nodes, spleen)

o Blood circulation

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13
Q

What are antigen presenting cells in blood circulation called?

A

plasmacytoid and myeloid DCs

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14
Q

What are the main TLR for identifying gram positive and gram negative bacteria?

A

Positive: TLR2
Negative: TLR4

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15
Q

Which TLR recognises adenovirus?

A

TLR9

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16
Q

What are the different types of antigen presenting cells and where are they found?

A

Dendritic cells:

  • Lymph nodes
  • Mucous Membranes
  • Blood

Langerhans cells
- Skin

Macrophages
- Various tissues

B cells (BCR)
- Lymphoid tissues
17
Q

What is the major histocompatibility complex (MHC)?

A

Set of cell surface proteins essential for the acquired immune system to recognise foreign molecules
- also called human leukocyte antigen

18
Q

Where are the MHC class I and class II found?

A

MHC Class I:
- expressed on all nucleated cells

MHC Class II:
- expressed on antigen presenting cells (dendritic, macrophaes, B cells)

19
Q

What type of expression do MHC genes show and why is this important?

A

Co-dominant expression

- increase in the number of different MHC molecules

20
Q

Why are MHC genes said to be polymorphic?

A

Many different alleles of the gene are present within a population
- don’t get wiped out by a single infection

21
Q

Which pathway is used to process microbes?

A

o Extracellular microbes: Exogenous pathways

o Intracellular microbes: Endogenous pathways

22
Q

Which MHC class is used to present antigens?

A

Extracellular microbes: presented by MHC Class II
molecules (HLA-DP, DQ, DR)

Intracellular microbes: presented by MHC Class I
molecules (HLA-A, B and C)

23
Q

Describe the endogenous microbe processing pathway.

A
  • Viral protein present in the cytosol
  • Marked for destruction by the proteasome
  • Proteasome-generated viral peptide transported to ER by TAP proteins
  • Formation of viral peptide-MHC class I complex if right match
  • Occurs in all cell types
  • APCs and non-APCs present peptides from intracellular pathogens to CD8+ T cells