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
Q

antigens and APCs enter the lymph node through

A

afferent lymphatics into the paracortical areas

26
Q

APCs and lymphocytes are attracted to the lymph nodes by

A

chemokines

27
Q

High endothelial Venules (HEV)

A

how naive lymphocytes get into the lymph node, located in paracortical area

28
Q

follicules of lymph node

A

where B cells are located in a lymph node

29
Q

cortex of lymph node

A

outer area of the lymph node where the follicules are

30
Q

paracortical area (of lymph node)

A

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
Q

germinal centers

A

where activated B cells undergo intense proliferation and differentiation into plasma cells with the help of T helper cells

32
Q

Spleen functions in immune responses to

A

blood born pathogens (not in the tissues); (especially good at responding to encapsulated bacteria)

33
Q

secondary function of the slpeen

A

dispose of old red blood cells

34
Q

Red pulp

A

majority of the spleen; sites of red blood disposal

35
Q

white pulp

A

collection of densely packed lymphocytes surrounding the arterioles running through the spleen

36
Q

periarteriolar lymphoid sheath (PALS)

A

sheath of lymphocytes around an arteriole; mainly T-cells

37
Q

follicules (of spleen)

A

adjacent to the PALS; contain B cells, may be germinal centers

38
Q

Marginal zone

A

surrounds the follicle; contains macrophages and resident, non-circulating B cells which are sensitive to circulating bacterial peptides

39
Q

what do macrophages and DCs within the marginal zone do

A

filter blood-borne microbes, soluble antigens, and antigen:antibody complexes which migrate to T cell areas and activate T cells after filtration

40
Q

When they become activated (in the LN), T cells and B cells both

A

move to the border of the follicle and T-cell zone, & T cells can provide their helper function to B cells

41
Q

Peripheral tolerance

A

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
Q

Peyer’s patches structure

A

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