lecture 11: introduction to the immune system Flashcards

1
Q

innate immunity

A
  • most plants and animals have some form of innate immunity eg: TLR, complement, lysozyme
  • rapid response, but low specificity
  • no requirement for MHC, B cell, T cells, but synergises with adaptive immunity in vertebrates
  • first line of defence against pathogens
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2
Q

complement system

A

= a group of proteins that circulate in the blood and when activated, help destroy pathogens through opsonization (marking pathogens for destruction), membrane attack complex formation and inflammation
- made of classical, lectin and alternative pathways

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3
Q

what triggers the different complement pathways

A

classical –> antibodies on antigens
lectin –> lectin bound to carbs
alternative –> activated spontaneously, by spontaneous

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4
Q

what are C3

A

central protein involved in all 3 pathways

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5
Q

toll like receptors

A
  • specific type of PRRs
  • they recognise conserved microbial structures and transmit signals to the nucleus to alter gene transcription
  • sense a variety of microbial molecules
  • signal via other adaptor proteins and activate transcription factors
  • gene transcription patterns are changed towards pro-inflammatory eg: cytokines are secreted
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6
Q

what does “the immune system is turned on by danger” mean

A
  • triggered by danger not by difference
  • microbial invasion to regions rich in leukocytes and TLR (or other PRR) triggers inflammation and immune action
  • both commensals and pathogens have PAMPs but commensals generally do not cause extensive inflammation and immune activation
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7
Q

commensals

A

refer to microorganisms, such as bacteria, fungi, or viruses, that live in or on a host organism (like humans) without causing harm and often provide some benefit to the host

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8
Q

how do innate and adaptive systems respond to commensals and pathogens

A
  • they respond to both commensals and pathogens
  • pathogens are intrinsically invasive
  • commensals are generally kept out by physical and chemical barriers
  • many pathogens act to suppress the immune system
  • in the gut, IgA is produced against both commensals and pathogens
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9
Q

adaptive immunity

A
  • slower initial response, but memory response rapid, high specificity
  • develops after exposure to a particular pathogen or antigen
  • has the ability to remember previous encounters with pathogens
  • major histocompatibility complex (MHC) dependent
  • requires B cells and/or T cells with somatically rearranged DNA
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10
Q

what are the components of the adaptive immune system and what do they arise from

A
  • bone marrow stem cells generate lineages of white blood cells (leukocytes)

main components:
- monocytes
- lymphocytes
- T cells
- B cells
- Macrophages
- Dendritic cells

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11
Q

myeloid cells: macrophages

A
  • differentiate from monocytes as they migrate into tissues
  • major role in phagocytosis
  • express MHC-I and MHC-II and act as antigen presenting cells
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12
Q

what do dendritic cells do

A
  • T cell activation
  • thymic tolerance
  • peripheral tolerance
  • T reg induction
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13
Q

dendritic cells

A
  • specialised immune cells that capture, process, and present antigens to T cells, thereby initiating adaptive immune responses
  • most potent of all antigen presenting cells (APC)
  • mainly found in tissues as ‘sentries’ (eg: skin)
  • carry antigen into lymph nodes for surveillance by T cells
  • if dendritic cells come into contact with microbes, toll like receptors will be activated
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14
Q

what is the role of CD4 and CD8 T cells

A
  • CD4 “helper” T cells help B cells to make antibody. they also help in the stimulation of CD8 T cell responses
  • CD8 T cells can become cytotoxic and kill virus infected or cancer cells
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15
Q

activation of T and B cells process

A
  1. dendritic cells activate helper T cells (CD4)
  2. helper T cells activate CD8 T cells and B cells
  3. cytotoxic T cells kill virally infected cells
    - produces enzymes that can kill cells, result in controlled death = apoptosis
  4. B cells produce antibody that neutralise toxins or ‘tag’ microbes for destruction
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