Innate Immunity – Complement, Innate Immune Cell Activation and Antigen Presentation Flashcards

1
Q

what are the two types of receptors on an innate immune cell?

A
  1. phagocytic receptors - (scavenger receptors, mannose receptors)
  2. Activation receptors- (toll like receptors)
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2
Q

describe the process of antigen processing

A
  1. During the process of phagocytosis proteins broken down to peptides
  2. Peptides displayed on the surface
  3. Present Peptides to T cells
  4. Inform T cells what pathogen was detected

*Phagocyte = Antigen presenting cell*

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3
Q

Know what APC, MHCClass2, Antigen and TCR refer to

A
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4
Q

Describe the process of MHC Class 2 presentation

A
  • Also known as Class II pathway
  • Pathogens, toxins, fragments that have been ingested/phagocytosed
  • Proteins digested to peptides in the phagolysosome
  • MHC class II in the endosome and endosome fuses with phagolysosome
  • Loaded onto MHC class II in the phagolysosome
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5
Q

MHC peptide complexes are recognized by what kind of cell?

A

T cells

TCR recognises presented peptides, binds and becomes activated

Communicating about the pathogen to the adaptive immune arm

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6
Q

What cells perform MHC Class 1 presentation?

A

all cells

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7
Q

Describe the MHC class 1 presentation

A
  • Also known as Class I pathway
  • Cells infected by virus or intracellular bacteria
  • Detected by host cells
  • Virally produced proteins digested by proteasome
  • Peptides transported into the endoplasmic reticulum
  • Loaded onto MHC class I in ER
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8
Q

What determines whether the antigen associates with MHC class 1 or 2?

A

–Depends on route by which antigen enters the cell

  • Intracellular – infects target cell – any cell a target - MHC class I
  • Extracellular – phagocytosed – only phagocytic cells involved – MHC class II
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9
Q

Differentiate MHC Class 1 and MHC class 2

A

•MHC class I

found on all cells

  • Presents material from intracellular organisms – viruses/bacteria/tumour proteins
  • As all nucleated cells can be infected – MHC class I can be found all cells
  • Upregulated during infection

•MHC class II

found on professional antigen presenting cells – macrophages, dendritic cells

  • Presents material from phagocytosed bacteria/viruses
  • Upregulated when APCs activated
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10
Q

MHC class 1 and 2 are encoded by what genes?

A

they are encoded by HLA genes

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11
Q

Describe the MHC diversity

A

the genes that encode for MHC class 1 and 2 are polygenic AND polymorphic

therefore, each individual has a unique set of MHCs with different ranges of peptide-binding specificites

They need different ranges of peptide recognition to fight all forms of infection

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12
Q

What is responsible for marking your own cells as ‘self’?

A

MHC class 1 found on all cells - marks you own cells as ‘self’ therefore your immune system won’t attack them

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13
Q

How do we prevent rejection of donor cells using our knowledge of MHC class 1 and 2 system ?

A

–T cells recognising non-self MHC

  • Donor MHC class I cells not recognised by recipient cytotoxic T cells and killed immediately
  • Donor Antigen presenting MHC Class II cells are attacked by recipient T helper cells and antibodies made
  • Prevention – HLA typing- this way we can choose a donor most suitable
  • Immunosuppressive drugs (T cells mainly)
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14
Q

What were the results of the ‘sweaty T shirt experiment’

A

•Women preferred smell of men with different MHC molecules – pheromone driven

•MHC and olfaction – MHC can present pheromone peptides – peptides presented determines attraction

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15
Q

If a pathogen breaches the epithelium, what works immediately?

A

Proteins in lymph/blood

  • Complement
  • Antibodies from previous encounters

then activation of innate immune cells - inflammation, phagocytosis, and antigen presentation

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16
Q

what is the complement system?

A

a series of proteins
with high plasma concentration that fights infection
- innate immune mechanism- non specific

•Plasma contains 20+ proteins that circulate in the blood: complement (C) proteins:

–that ‘complement’ antibody action

–Complement proteins synthesised in liver

–Inactive proteins until activated by recognising bacteria/pathogen

–Cleaved by a protease to active form

–Majority once activated cleave and activate another part of the cascade

17
Q

What are C3a,b,and C5 responsible for immunologically?

A

C3a= inglammaotry response - proteins promote an inflammtory reponse - mast cells are degranulated causing increased vascular permeability - cause vasodilation, vascular permeability, chemoattraction and homing

C3b= opsonisation = C3b is left on the microbial cell wall (as opsonin) and is recognised by phagocytes who quickly eat the cell

C5= lysis = pops the cell by forming a multiprotein complex with C5-C9 and assembles on the surface of the pathogen to form a big whole. cell death occurs via loss of cell integrity

18
Q

what is the classical and alternative pathway for complement activation?

A

classical pathway = triggered by formation of the antibody antigen complex

Alternative pathway- where a component of complement binds to pathogen surface thus tagging it for destruction

19
Q

describe the general immune system response from the instant a pathogen enters …

A