Adaptive Immunity Flashcards

1
Q

Transition from innate –> adaptive immunity

A

Occurs when antigen-presenting cells interact with a T or B cell that is specific for a given antigen

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2
Q

What is an antigen?

A
  • Any molecule to which an antibody can specifically bind
  • Generates antibodies
  • Can be proteins, carbohydrates or nucleic acids
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3
Q

What is an antibody?

A
  • Effector molecules produced by B cells that is specific for a given antigen
  • When an Ab binds to it’s antigen, it tags the pathogen for destruction by phagocytes (like macrophages & B cells)
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4
Q

Antigen presentation

A
  • T cells can’t recognize “native” antigen-only processed fragments of antigen
  • APCs pick up antigens, process them & then present it on MHC proteins
  • MHC proteins were discovered by failed tissue transplantations
  • MHC1 is expressed on almost all nucleated cells & MHC2 is only expressed on professional APCs (macrophages, dendritic cells & B cells)
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5
Q

When/where do APCs process antigens?

A
  • APCs begin processing antigens right after they have engulfed a pathogen
  • They will then travel through the lymphatics to a lymph node (or through blood to the spleen) where they will present the antigens to naive T cells
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6
Q

T cell activation in the lymph nodes

A
  • Each T cell has only one specificity of T cell receptor

- A T cell receptor will only react with one antigen

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7
Q

Generation of diversity

A
  1. Germline theory
    - Separate gene for each distinct receptor
  2. Somatic diversification theory
    - Recombination of a limited number of gene sequences leading to a large number of distinct receptors
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8
Q

Clonal selection

A

A hypothesis which states that an individual lymphocyte (specifically, a B cell) expresses receptors specific to the distinct antigen, determined before the antibody ever encounters the antigen

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9
Q

B and T cell development

A
  • Some will be auto reactive & target self molecules
  • Both T and B cells undergo NEGATIVE selection to eliminate these cells (apoptosis)
  • T cells also undergo POSITIVE selection; needs to be able to recognize our own MHC or else its useless
  • Reduces chance of autoimmunity
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10
Q

T cell development

A
  • T cell development occurs in the thymus
    • T cell precursors travel from the bone marrow –> thymus to develop
    • Mature T cells leave the thymus & travel to secondary lymphoid tissues (where they can surveil for APCs)
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11
Q

Types of T cells (x2)

A

CD4+ “helper” T cells

  • They activate macrophages to kill the bacteria they have inside
  • Activate T cells to produce antibodies
  • Recruit neutrophils

CD8+ “killer” T cells
- They find infected cells and cause the cells to undergo apoptosis

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12
Q

Activation of B cells

A
  • Antigen recognition induces expression of effector molecules by the T cell, which activates the B cell
  • Differentiation to resting memory cells & antibody-secreting plasma cells
    • Produce massive amounts of ER to produce lots of antibodies
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13
Q

B cells can sometimes be activated without T cells

A
  • Activation when their receptors are cross-linked by antigens
    • Receptors act kinda like an antibody
  • Alone this is a weak signal, but if you bring them together –> looks like a strong signal
  • Even things that might not be able to bind to a T cell receptor, can sometimes activate a B cell aka a T cell independent antigen
    - T cell independent antigens do not make as good as of an immune response as a T cell dependent antigen
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14
Q

Functions of antibodies

A
  1. Neutralization: coat the pathogen with antibodies so the pathogen can’t bind to the epithelium
  2. Opsonization: antibody binding activating the complement cascade; promotes phagocytosis into a macrophage for killing
  3. Complement activation: if an antibody binds, the complement system is activated
  • Antibodies can also bind to the surface of one of our cells
    • Fc receptors on NK cells recognize bound antibodies
    • Causes NK cells to release its toxic granules –> apoptosis (doesn’t release the virus particles, preventing spread)
    • Now the virus infected cell is gone
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15
Q

Types of antibodies (x4)

A
  1. IgG
    • Workhorse of the antibodies, does everything, immune memory, found almost everywhere, provides immunity to fetuses
  2. IgA
    • Dimer, mucosal antibody, secreted out into lumen of respiratory/GI tracts, doesn’t go to fetus
  3. IgM
    • First antibody produced (in primary immune response), found in blood, very big = doesn’t cross in or out of blood
  4. IgE
    • Associated with allergy & parasite defence (mast cells have IgE), found at body interfaces - found under skin –> hives & itchy skin

NOTE: dimeric IgA makes its way into the breast milk
- Breastfed infants benefit from mom’s IgA that they can now take into the lumen of their GI tract

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