Adaptive immunity- extracellular Flashcards

1
Q

which cell act was a bridge between the immune and adaptive immune system

A

antigen presenting cells

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2
Q

if naive T cells and pathogen meet

A

no response

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3
Q

only way T cells can be activated is by

A

antigen presenting elsl

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4
Q

APCS

A

phagocytose and process the microbe and present it to the Naïve T cell so they can recognise pathogen/tumour cell

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5
Q

naive T cell

A

T cell that have no previously encountered the antigen

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6
Q

effector T cell

A

T cells that have previously encountered the antigen are capable of performing the effector functions during an immune response

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7
Q

Antigen presenting cells role

A
  • Sense the pathogen
  • Capture pathogen
  • Process pathogen
  • Present the pathogen to T cells
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8
Q

name 4 APC

A

dendritic cells
langerhans
macrophages
B cells

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9
Q

dendritic cells and langerhans (dendritic cell specialised for the skin) present the pathogen to ……………. and have what function

A

present to naive T cells

Function: T cell response against most pathogens

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10
Q

macrophages and B cells present the pathogen to …………….

A

present to effector T cells

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11
Q

function of macrophages

A

phagocytic activities

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12
Q

function ofB cells

A

antibody response (humeral)

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13
Q

APC are found in strategic locations

A
  • Mucosal membrane (gut, lung)
    o Mucosal associated lymphoid tissue (MALT)
  • Skin (Langerhans cells)
    o Skin associated lymphoid tissue)
  • Blood (plasmacytoid cells)
  • Lymph nodes (follicular dendritic cells)
  • Spleen
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14
Q

pathogen capture method of APC

A
  • Phagocytosis (whole microbe)

- Micropinocytosis (soluble particles)

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15
Q

2 types of microbes

A
  • Extracellular
    o Fungal
    o protozoa
    o Most bacteria
  • Intracellular
    o Virus
    o TB
    o Cancer
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16
Q

PRRS recongise

A

intracellular and extracellular pathogens PAMPs

17
Q

TLR recognise extracellular pathogens

A

TLR1,2,6,4,5,11

- TLR4- Neisseria meningitidis- sepsis

18
Q

TLR recognise intracellular pathogens

A

TLR3,7,8,9

19
Q

how do APC activate the adaptive immune system

A
  1. Macrophages and APC recognise pathogen
  2. APC use lymphatics to get to lymphoid tissue
  3. APC presents to T cells
20
Q

Major histocompatibility complexes (MHC) molecules are a type of

A

human leukocyte antigen

21
Q

HLA

A

human body version of MHC

- how pathogens are presented to naive T cells

22
Q

MHC I

A
  • Expressed on all nucleated cells
  • CD8 cytotoxic T cells
  • Kill intracellular pathogens
    • Virus’
    • TB
    • Cancers
23
Q

MHC II

A
  • Expressed on APCs, dendritic cells, macrophages and B cells
  • CD4 T helper cells
    • Fungal
    • Bacteria
    • Parasitic
24
Q

key features of MHC molecules

A
  • Co-dominant expression
    o Both MHC class I and II parental molecules are co-expressed in each individuals (6 of each class)
  • Polymorphic genes (diff alleles)
    o Different individuals present and respond to different microbes
25
Q

Antigen presenting cells present intracellular microbes via MHC class I molecules

A

HLA-A, B and C

26
Q

Extracellular microbes presented by MHC class II molecules

A

HLA-DP, HLA- DQ, HLA-DR

27
Q

processing of intracellular microbes (MHC I)

A
  1. Viral proteins present in the cytosol
  2. Marked for destruction by proteasome
  3. Proteasomes-generated viral peptides transported to ER by TAP proteins
  4. Formation of viral peptide- MHC class I complex if right match (coded in genome)
  5. APCS and non-APC present peptides from intracellular pathogens to CD8+ T cells
  6. T cells only react when sensing a foreign peptide
  7. Also present self peptides in this way
28
Q
Processing of extracellular microbes
Exogenous pathway (MHC II)
A
  1. Microbes captured by phagocytosis or micropinocytosis
  2. Degradation in small peptides in the endosome
  3. Peptide rich vesicles fuse with vesicles containing MHC class II molecules
  4. Formation of peptide MHC class II complex if right match
  5. APCs present peptides extracellular pathogens to CD4+ T cells
29
Q

MHC I found on

A

all cell types

30
Q

MHC II found on

A

APCs- dendritic, B cells and macrophages

31
Q

peptide bonding cleft on the MHC molecules

A

highly variable region with highly polymorphic residues (coded for in the genome)

32
Q

MHC I occurs as an α chain composed of three domains

A

—α1, α2, and α3.

33
Q

MHC class II is formed of

A

two chains, α and β, each having two domains—α1 and α2 and β1 and β2—each chain having a transmembrane domain, α2 and β2, respectively, anchoring the MHC class II molecule to the cell membrane.

34
Q

no individual has the same set of

A

mHC moleculen

35
Q

Individuals have different susceptibilities rot infection

A

o Strong vs weak immune response against infectious microbes
 Pregnant
 Immunosuppressed
 Children

36
Q

HLA molecule mismatch between donor and recipient (allograft) is

A

a major cause for organ transplant rejection

GRAFT VERSUS HOST REACTION (GVH)

37
Q

HLA association with autoimmune disease

A
  • Ankylosingspondylitis
    o HLA-B27 -> 90% of patients
  • Insulin-Dependent Diabetes Mellitus
    o HLADQ2 -> 50-75% of patients