Lymphoid Anatomy Flashcards

1
Q

central lymphoid organs

A

thymus and bone marrow

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2
Q

peripheral lymphoid organs

A

adenoid, tonsil, lymph nodes, appendix, spleen, mucosal

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3
Q

B and T cells originate where

A

bone marrow

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4
Q

B cell mature where

A

bone marrow and are continually produced even in adults

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5
Q

where do T cell mature

A

thymus-slows down as individuals age but T cell numbers are maintained outside the central lymphoid organs

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6
Q

adaptive immunity occurs when

A

a lymphocyte meets its corresponding antigen in the peripheral lymphoid tissue

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7
Q

purpose of lymphoid tissue

A

Supports lymphopoiesis
Supports development of incredibly diverse repertoire of antigen-specific lymphocytes
Critically important for both central & peripheral tolerance
Provides sustaining signals for lymphocyte survival

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8
Q

central lymphoid tissue purpose

A

Responsible for lymphopoiesis
Responsible for central tolerance
B cells: Bone Marrow
T cells: Thymus

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9
Q

peripheral lymphoid tissues purpose

A

Mixture of B & T cells
Supports circulating lymphocyte survival
Activation of naïve lymphocytes
Peripheral Tolerance

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10
Q

Stromal cells

A

Stromal cells in the bone marrow, are critically important to B cell development. Provide maturation factors such as FLT3 ligand, IL-7, Stem-Cell Factor (SCF) & CXCL12

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11
Q

final stage of immature B cells developing to mature B-cells occurs where?

A

peripheral lymphoid organs

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12
Q

Central Tolerance

A

immature B cells in the BM are tested for reactivity to self antigens or auto reactivity and are eliminated if autoreactive

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13
Q

thymus cortex

A

the outer cortical region; contains only immature thymocytes & scattered macrophages; most t-cell development occurs here

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14
Q

thymus medulla

A

the inner region; more mature single positive thymocytes, dendritic cells & macrophages

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15
Q

lack of Thymus

A

no T cell development despite lymphoid progenitors

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16
Q

young vs old thymus

A

The thymus is fully developed at birth
Rate of T-cell production is greatest before puberty
After puberty, the thymus begins to shrink & the production of new T cells is lower but not entirely absent

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17
Q

when does the beta chain rearrangement of the T-cell receptor take place

A

during the double negative phase

18
Q

when does the alpha chain rearrangement take place

A

during the puble positive phase

19
Q

T-cell development relays on

A

timely expression of various surface and signaling molecules

20
Q

thymic cortal stroma

A

network of epithelia where the T cell precursors reside; provides unique microenvironment for T- cell development (like B cell stromal cells); has epithelial cells with long branching process that express both MHC I and MHC II on their surface.

21
Q

corticomedullary junction of the thymus

A

where the t cell progenitors enter

22
Q

positive selection

A

if the double positive T cell does recognize self-peptide;self-MHC complexes, than it will drop one of the co-receptors and become either CD4+ or CD8+ single positive T-cells and migrate to the medulla

23
Q

Negative selection

A

If the single positive T-cell recognizes self-peptide:self-MHC too strongly, then it will undergo apoptosis. If it does not it will be exported from the thymus to the periphery

24
Q

central tolerance

A

98% of thymocytes that develop in the thymus also die in the thymus by apoptosis. includes positive and negative selection

25
antigens and APCs enter the lymph node through
afferent lymphatics into the paracortical areas
26
APCs and lymphocytes are attracted to the lymph nodes by
chemokines
27
High endothelial Venules (HEV)
how naive lymphocytes get into the lymph node, located in paracortical area
28
follicules of lymph node
where B cells are located in a lymph node
29
cortex of lymph node
outer area of the lymph node where the follicules are
30
paracortical area (of lymph node)
aka deep cortex; where the T cells are diffusely scattered; also where free antigen gets "trapped" on resident DCs and macrophages; also where migrating DC's bring their antigens. Great meeting spot for T cells and APCs so T cells can become activated.
31
germinal centers
where activated B cells undergo intense proliferation and differentiation into plasma cells with the help of T helper cells
32
Spleen functions in immune responses to
blood born pathogens (not in the tissues); (especially good at responding to encapsulated bacteria)
33
secondary function of the slpeen
dispose of old red blood cells
34
Red pulp
majority of the spleen; sites of red blood disposal
35
white pulp
collection of densely packed lymphocytes surrounding the arterioles running through the spleen
36
periarteriolar lymphoid sheath (PALS)
sheath of lymphocytes around an arteriole; mainly T-cells
37
follicules (of spleen)
adjacent to the PALS; contain B cells, may be germinal centers
38
Marginal zone
surrounds the follicle; contains macrophages and resident, non-circulating B cells which are sensitive to circulating bacterial peptides
39
what do macrophages and DCs within the marginal zone do
filter blood-borne microbes, soluble antigens, and antigen:antibody complexes which migrate to T cell areas and activate T cells after filtration
40
When they become activated (in the LN), T cells and B cells both
move to the border of the follicle and T-cell zone, & T cells can provide their helper function to B cells
41
Peripheral tolerance
In the absence of an infection, mature B & T cells that encounter a strongly cross-linking antigen in the peripheral lymphoid organs will undergo clonal deletion or anergy
42
Peyer's patches structure
Peyer’s Patches have the structure of lymphoid follicles with parafollicular regions & germinal centers. However they are not encapsulated & have lymph & blood-independent entry of antigen from the lumen