Lecture 10: Adaptive Immunity and Immune Recognition Flashcards

1
Q

Outline the general features and components of adaptive immunity.

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2
Q

Mention and describe the phases of adaptive immunity.

A
  • Priming phase: the first time the adaptive immune system encounters an antigen
  • Effector phase: activates adaptive cells differentiate into effector cells to fight infection and eliminate the pathogen
  • Contraction phase: most effector cells die following clearance of the pathogen
  • Memory phase: some long-lived memory cells remain to ensure that the immune system can respond faster and stronger upon reencountering that pathogen
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3
Q

Recall the cells of adaptive immunity.

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4
Q

Recall the characteristic of adaptive immunity.

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5
Q

_______________ comprises the cells of the adaptive immune system.

A

The lymphoid lineage

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6
Q

Describe B cells.

A
  • Derived from lymphoid progenitor
  • Mature in the bone marrow
  • CD19 positive (surface biomarker)
  • Each B cell has around 100,000 BCRs, all with the same specificity
    • BCR engagement leads to proliferation and transition into plasma cells (‘effector B cells’)
  • Plasma cells secrete soluble BCR (-antibodies) that have same specificity as surface receptor
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7
Q

Describe T cells.

A
  • derived from lymphoid progenitor in the bone marrow
  • develop and become educated in the thymus
  • express co-receptors: either CD4 (MHC class II restricted) or CD8 (MHC class I restricted)
  • recognise antigen via distinct cell surface receptors (α/ß T cell receptor) with high degree of specificity
    • requires processing of antigen by the APC and presentation on MHC
  • T cells need to be activated to exert function
    • activated T cells can leave the blood and survey the periphery
    • CD4+ Helper T cells: regulators of immune responses
    • CD8+ Cytotoxic T cells: cytotoxic (perforin, granzymes)
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8
Q

Recall the functional polarization of helper T cells.

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9
Q

Recall the unique receptors on lymphocytes.

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10
Q

Recall the anatomy of a lymph node.

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11
Q

Recall how antigens are encountered by lymphocytes in the body.

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12
Q

What are antigens and epitopes?

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13
Q

What are eptiopes?

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14
Q

What are immunogens? What are the factors affecting immunogenicity?

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15
Q

What are hapten-carrier complexes?

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16
Q

Recall the effect of hapten carrier complexes in immunogenicity.

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17
Q

Recall the innate vs adaptive immune recognition

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18
Q

Recall the receptor characteristics of innate vs adaptive immune recognition.

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19
Q

Describe the basics of T cell receptor recognition.

A
  • T cell receptors antigen in the form of a complex of a foreign peptide bound to an MHC molecule.
  • Peptides must be processed to be presented, peptides are stably bound to MHC molecules, serving to stabilise the MHC molecule on the cell surface.
20
Q

Recall the two type of T cell receptor recognition (CD4 and CD8)

A
21
Q

Recall the mechanism behind immunoglobulin recognition.

A

Immunoglobulins bin antigen via contacts in their variable regions that are complementary to the size and the shape of antigen. Majority of BCR epitopes are conformational (discontinuous)

Immunoglobulins (BCR/Abs) bind to conformational shapes on the surfaces of antigens using a variety of non-covalent forces.

22
Q

Immunoglobulins (BCR/Abs) bind to conformational shapes on the surfaces of antigens using a variety of _______________.

A

non-covalent forces.