Lymphocyte receptors, B cells and antibodies Flashcards

1
Q

for B cells and T cells, which part of their receptors are constant and which part is variable

A

tip is usually variable

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2
Q

variable region of antibody is made out of what parts

A

variable
diversity
joining

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3
Q

what is junctional diversity

A

junction between variable/diversity/joining segments is not precise-> nucleotides are added and removed from junctions during rearrangement

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4
Q

what happens when a b cell is activated

A

differentiation into plasma cell that produces antibodies

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5
Q

structure of antibody

A

2 heavy chains inside (joined by disulfide bonds)
2 light chains on the outside (also joined by disulfide bonds)
variable regions at the top only

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6
Q

what do variable and constant regions usually confer

A

variable regions determine specificity

constant regions determine class

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7
Q

classes of antibodies; how are subclasses named

A

A, D,E,G,M

igA1, igA2,3,4.. etc

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8
Q

antibody functions

A

neutralisation of toxins/viruses (block interaction with other cells)
opsonise
activate component cascade
particle agglutination

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9
Q

IgG characteristics/function and subclasses. how are the subclasses arranged

A

main serum antibody
specific igG measured in response to vaccine
opsonisation
agglutination to pathogens-> target for NK (antibody dependent cellular toxicity)
IgG1,2,3,4 (in decreasing order of abundance)

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10
Q

igA forms, how does it move into the gut and what does it do there

A

igA is a monomer in serum
dimer on mucosal surface, dimer is formed by J chain
igA has secretory component (Carbohydrate-rich)-> attaches to basolateral surface of epithelial gut cell-> transport into gut lumen -> agglutinates bacteria -> retains antigen by attaching to mucosal surface of gut

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11
Q

igM characteristics

A

first antibody made in immune responses
pentameric
good for agglutination

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12
Q

igE characteristics

A

mast cells have igE fc receptor -> when allergens X-link with igE-> mast cell releases granules
people with allergies have lots of igE

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13
Q

what antibodies do b cells have on their surface

A

igM and igD

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14
Q

how does affinity maturation take place

A

germinal centres contain dividing B cells-> if B cells encounter specific antigen + help from Th2 cells-> rapid division-> somatic hypermutation (mutate ig variable region)-> high affinity variants selected-> affinity maturation

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15
Q

where does class switching take place

A

in germinal centres in secondary lymphoid organs

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16
Q

what kind of cells are produced in germinal centres

A
b memory cells -> quiescent circulating cells-> affinity matured/class switched 
plasma cells-> go to bone marrow or intestine/long lived
17
Q

primary vs secondary immune response

A
primary: igM rises first-> class switch to igG which peaks after 15 days 
secondary-> igM rises first-> class switch to igG which peaks to a greater level by 15 days
18
Q

are normal b cell populations monoclonal or polycolonal? what about memory clones?

A

polyclonal

polyclonal too, due to somatic hypermutation in germinal centre

19
Q

what is a chimeric antibody? example

A

mouse monoclonal engineered-> variable regions are associated with human constant regions; ends with -ximab
eg rituximab for B cell lymphoma

20
Q

what is a humanised antibody? example

A

only variable region is from mouse;
ends with -zumab
omalizumab for servere asthma allergies

21
Q

what are human monoclonal antibodies? example

A

fully human
-umab
adalimumab for inflammatory diseases

22
Q

what happens in haemolytic disease of newborn;

solution

A

mother who is rh- has igG against rh+ following exposure to rh in first pregnancy-> in second pregnancy, cross placental transfer of antibodies to fetus-> RBC lysis
plasmapheresis: igG removed from baby’s blood