Lecture 1 Immunology Flashcards

1
Q

what did Hooke, Van Leeuwenhoek and Jenner discover respectively?

A

Hooke 1665; micrographia “cells” at 10/20X
Van Leeuwenhoek 1674: animalcules, 200X, lighting
Jenner 1796: cowpox immunisation effect against smallpox

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2
Q

what did Pasteur 1860 discover

A

germ theory- pasteurisation and rabies vaccination

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3
Q

what did Kariko and Weissman 2023 discover

A

mRNA vaccines

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4
Q

describe how SARS-CoV-2 can be spread, and its mode of action

A

spread via air droplet suspensions. binds to ACE2 receptors on epithelial cells, and via protease can enter the cell (cleavage of the S protein, and hence activation of the S2 domain)

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5
Q

differentiate between innate and adaptive immune sys

A

innate = non specific + rapid response, i.e barriers (mucosa, HCL in stomach)

adaptive = specific, slow, learned. i.e B cells, T cells, Plasma cells

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6
Q

what is the progression of the innate immune response

A

infection, recognition of pathogens by sensors, activation of cells and inflammation, removal of the infectious agent

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7
Q

what is the progression of the adaptive immune response

A

infection, stimulation of T and B cells in lymphoid organs, expansion and training of effector T and B cells. Migration to infection site , removal of infectious agent

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8
Q

what are the lines of defence of innate response

A

skin(epithelia), pH, mucosa, enzymes (i.e lysozyme), commensals

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9
Q

how does lysozyme work for microbial containment

A

lysozyme breaks down peptidoglycan in gram pos cells .

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10
Q

describe the mucosa layers and how they defect pathogens

A

outer mucus layer traps most pathogens. motile bacteria can make their way through second layer of mucous- where there is IgA antibodies and antimicrobial proteins. IgA bind to pathogens and cause release of cytokines

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11
Q

PAMPS-PRRS (pathogen recognition receptors)

A

PRRs are receptors which recognise PAMPS (pathogen associated molecular patterns) which are microbial components such as lipopeptides, peptidoglycan, LPS, flagellin.

TLR2 is expressed on immune cells such as macrophages, and it can detect peptidoglycan in gram pos cells.

TLR4 is also expressed on immune cells and detects LPS on gram neg cells

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12
Q

what happens when a TLR2/TLR4 detects PGN or LPS

A

release of cytokines to initiate inflammatory response

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13
Q

describe the TLR structure

A

leucine rich repeat motifs, and cysteine rich flanking motif. TIR domain within the cell

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14
Q

describe peyer’s patches

A

areas in the large intestine- aggregates of lymphoid tissue T cell zone, B cell zone and lacteals

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15
Q

main parts of spleen?

A

capsule, red pulp, white pulp, T cell zone, B cell zone

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16
Q

parts + function of the thymus

A

capsule, cortex, medulla

T lymphocytes mature functionally here

17
Q

primary lymphoid tissues

A

bone marrow, thymus

18
Q

secondary lymphoid tissues

A

mucosa associated lymphoid tissue (MALT) i.e resp tract, digestive system, urinary tract, saliva .
Lymph nodes, spleen