Mucosal immunity Flashcards

(57 cards)

1
Q

what are primary lymphoid organs

A

sites where b and T cells are made and matured

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

where are the primary lymphoid organs

A

bone marrow
thymus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what are the secondary lymphoid organs

A

sites where b and T cells can recognise antigen and become activated to fight infection or cancer

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

where are the secondary lymphoid organs

A

lymph nodes
spleen
mucosa associated lymphoid tissues/MALTs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

capsulated lymphoid tissues

A

lymph nodes
spleen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

non-capsulated lymphoid organs

A

mucosa associated lymphoid tissues
50% of bodies lymphoid tissue

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what are capsulated lymphoid tissues designed for

A

to control what comes in from outside and keep things trapped inside

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

function of the spleen

A

as a filter for blood
not supplied by lymphatic vessels
responds to systemic infections
more lymphocytes flow through spleen than all lymph nodes at any given time

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

how do antigens and lymphocytes enter the spleen

A

via the splenic artery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

2 distinct regions of the spleen

A

white pulp
red pulp
separated by a diffuse marginal zone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

differences between lymph nodes and spleen

A

lymphocytes enter via artery
and immune response occurs in the periarteriolar lymphoid sheath

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

red pulp function

A

contains mainly macrophages, RBCs and some lymphocytes
old and damaged RBCs are phagocytose in the red pulp

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

white pulp function

A

mainly surrounds arteries in the spleen
forms periarteriolar lymphoid sheath
predominantly T cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

marginal zone function

A

at the edge of the PALS
made of mainly B cells
contain primary lymphoid follicles

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

process of immune response in the spleen

A

foreign antigen carried into the spleen from the splenic artery into the marginal zone and captured by dendritic cells
dendritic cells and T cells move to the PALS from the splenic artery
PALS the dendritic activate T helper cells
active T helper cells activate B cells and activated B and helper T move to the primary follicles in the marginal zone
leads to the production of a secondary follicle with germinal centre

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

lymph nodes

A

clustered at junctions of lymphatic channels, entrap pathogens entering the lymphatic system from the tissues
bean-shaped structures, comprising a mesh-like reticular framework , packed with lymphocytes, macrophages and dendritic cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

lymph nodes and immune response

A

lymph flows into the node through lymphatic channels, empty into the sub capsular space carrying APCs and free antigens
lymph percolate inwards, allows phagocytic cells to entrap any bacteria in the lymphatic fluid
a single efferent vessel leaves the lymph node
lymph nodes enlarge when immune response occurs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

fluid in the efferent lymphatic vessel

A

contains antibodies and 50x higher concentration of lymphocytes due to proliferation of lymphocytes within the node

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

production of secondary follicle in lymph node

A

antigen and APC from tissue travel to lymph node in the lymphatic fluid
antigens processed by resident dendritic cells in the paracortex
dendritic cells and B cells activate antigen specific T helper cells
B cells also activated in the paracortex by antigen directly via the BCR and any helper T cells
activated B and helper T form foci with proliferating B cells
B cells and helper T cells migrate to primary follicles of the cortex and interact with follicular dendritic cells
production of secondary follicle with germinal centre and production of plasma cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

what are lymphoid follicles

A

collections of lymphocytes and dendritic cells, in all secondary lymphoid tissue

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

primary follicles

A

collection of mainly inactive B cells, macrophages and follicular dendritic cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

what occurs when germinal centres are formed

A

the follicle is called a secondary follicle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

what happens when activate dB cells and helper T cells move into follicles

A

proliferate forming germinal centres

24
Q

germinal centres

A

B cells proliferate and undergo somatic hypermutation to make better antibodies
inactive B cells pushed towards age to form mantle zone
B cells surrounded by cuff of T helper cells

25
what is occurring in the dark zone
cell proliferation
26
what is occurring in the light zone
cell death
27
somatic hypermutation
immunoglobulin gene sequences are further mutated after rearrangement and binding to their antigen introduces point mutations at a high rate V sequences not C sequences are mutated B cells mutate in dark zone of a germinal centre
28
advantages of V sequence mutations
more diversity higher affinity
29
because the mutations are random what may happen
some BCRs have detrimental some B cells have favourable mutations
30
BR detrimental mutations
less able to bind to the antigen can recognise self proteins leads to apoptosis of B cells
31
favourable mutations
many Able to bind the foreign antigen- increased affinity leads to selection of B cells with highest affinity BCRs through interaction of follicular T helper cells, affinity maturation
32
BCR less good at binding antigen
doesn't bind antigen as well as other BCRs cell doesn't capture, process and present antigen to T cell B cel doesn't receive T cell help and dies
33
BCR better at binding antigen
binds antigen better than others Cell captures, process and presents antigen to the T cell B cell receives T cell help, proliferates and differentiates to plasma cell
34
what follows somatic hypermutation and selection of high affinity B cell by affinity maturation
B cells move further into the light zone receive a second survival signal from a T helper cell causes differentiation into either plasma cells or memory B cells can induce class switching of antibody
35
class switching
B cells make different types or isotopes with different constant regions each isotope has different characteristics and binds to different Fc receptors on cells
36
what does the variable region do
determine antigen specificity
37
what does the constant region do
determine antibody class
38
label the antibody
top left up to the first dip= variable region bottom left fro the dip to the bottom= constant region bottom of two chains= Fc region blue= heavy chain orange=light chain specific hole in the top= FAB region
39
which kinds of antibodies are important in MALT
IgA and IgD
40
if barriers are breached what do mucosa have
draining lymph nodes MALTs perpetually activated innate and adaptive immune cells throughout epithelium and lamina propria
41
what do MALTs do
defend body against pathogen entry via mucous membranes more plasma B cells than in lymph, spleen and. bone marrow
42
2 types of MALT tissue
BALTs GALTS
43
what does BALT stand for
bronchus-associated lymphoid tissue
44
what does GALT stand for
gut-associated lymphoid tissue
45
GALTs
peyers patches in the small intestine isolated lymphoid follicles lamina propria immune cells appendix palatine tonsils adenoids lingual tonsils all support the mesenteric lymph node
46
where are tonsils found q
lingual palatine nasopharyngeal
47
tonsils
nodular structure with meshwork of reticular cells, macrophages, granulocytes and mast cells B cells organised into discrete follicles and germinal centres surrounded by cuff of T cells defends against antigens entering nasal and oral epithelia
48
inductive sites
where B and T cells re primed by antigen and differentiate into effector cell
49
effector sites
where B and T cells migrate to carry out effector function to clear pathogens
50
Peyers patches
inductive sites 30-40 lymphoid nodules distal small intestine nodules contain follicles developing into germinal centres on antigen exposure closely associated with intestinal epithelium
51
microfold cells
M cells occur at inductive sites have broad process in contact with lumen deep invagination or pocked in basal membrane filled with B cells, T cells, dendritic and macrophages
52
antigen in M cells
from the lumen of digestive, respiratory or urinary tract is phagocytosed transported and released into basolateral pocket of cell antigen taken up by dendritic cells leading to activation or tolerisation of T and B cells in lamina propria
53
examples of immune cells
goblet cytotoxic t cells plasma
54
goblet cells
produce mucu
55
cytotoxic T cells
rapidly eliminate infected epithelial cells
56
plasma cells
secrete IgA and IgD
57
what is an AMP
antimicrobial peptide