First Aid, Chapter 2 Cells Involved in Immune Responses, Lymphocytes Flashcards

1
Q

What are the 3 types of lymphocytes?

A

B cells, T cells, and NK cells

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2
Q

What are the general roles of helper T lymphocytes (CD4+ Th)? What are the markers?

A

Stimulate B-cell growth; secrete cytokines to activate macrophages; MHCII-restricted; markers CD3+/CD4+/CD8–.

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3
Q

What are the major CD4+ families?

A

Th1, Th2, Th17, Th9, Tfh, Treg

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4
Q

What are Th1 cells induced by? What do they produce? What are the transcription factors? What is the major function? What do they express? What diseases are they associated with?

A
Induced by: IL-12, IL-27, IL-18
Produce: IFNy, IL-2, TNF
Transcription factors: Tbet, STAT4, STAT1
Major function: Intracellular defense
Express: CXCR3, CCR5
Associated with: DM type 1, MS
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5
Q

What are Th2 cells induced by? What do they produce? What are the transcription factors? What is the major function?

A

Induced by: IL-4, IL-25, IL-33, TSLP
Produce: IL-4, 5, 13; IL-6, 10, 21, 25, 31, 33
Transcription factors; GATA3, STAT6, STAT5
Major function: humoral immunity, antiparasitic, allergy

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6
Q

What are Th17 cells induced by? What do they produce? What are the transcription factors? What is the major function? What do they express? What diseases are they associated with?

A

Induced by: IL-6, IL-1, 21, 23, TGFB
Produce: IL-17, IL-1, 6, 21, 22, TNFa, GM-CSF
Transcription factors: RORyT, STAT3
Major function: Extracellular defense; neutrophil recruitment; autoimmunit
Express: CCR6
Associated with: RA, IBD, MS, and psoriasis

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7
Q

What are Treg cells induced by? What do they produce? What are the transcription factors? What is the major function? What are the 2 Treg subsets? What do they produce to suppress other T cells?

A

Induced by: TGFB and retinoic acid
Produce: IL-10, TGFB
Transcription factors; FOXP3, STAT5
Major function: Immunosuppression, prevents autoimmunity
Subsets: natural Tregs, Induced Tregs
Do not make IL-2, use cytotoxic T-lymphocyte antigen 4 (CTLA4) to suppress other T cells

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8
Q

What are Th9 cells induced by? What do they produce? What is required for their differentiation?

A

Induced by: transforming growth factor beta (TGFB) and IL-4
Produce: IL-9 +/- IL-4
Require IRF4 and PU.1 for differentiation

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9
Q

Where are Tfh (follicular helper T cells) located? What is their role? What is it mediated by? What does it produce?

A
  • Located in the follicles of active germinal centers.
  • Play a major role in helping B cells make antibodies.
  • Mediated by transcription factor Bcl-6 (which causes downregulation of CCR7 and upregulation of CXCR5)
  • Produce IL-21.
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10
Q

Where are natural Tregs derived? What are they developed in response to? What do they express? What is their function?

A

Thymically derived and develop in response to thymically presented autologous antigens Constitutively express IL-2-Rα(CD25+) FOXP3+ Mediate self-tolerance

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11
Q

Where are induced Tregs derived? What are they developed in response to? What do they express? What types of cells do they include?

A

Peripherally derived and develop in response to peripherally expressed self-antigens and external antigens Inducible IL-2–Rα(CD25) expression Include: Tr1(produce IL-10; involved in mechanism of immunotherapy), Th3 (produce TGFβ; in gut; important in IgA production)

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12
Q

How do cytolytic T lymphocytes (CTLs and CD8) kill virally infectedcells and tumor cells? What do they express? What pathogenesis are they involved in? What do they use as a transcription factor? What markers do they have?

A

Kill viral-infected cells and tumor cells via perforin and granzyme; express IFN, TNF, and lymphotoxin; harder to activate than CD4s; involved in allograft rejection; use eomesodermin homologs (EOMES) as a transcription factor; MHCIrestricted; markers CD3+/CD8+/CD4–.

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13
Q

Where to γδ T cells develop? Do they have a large diversity? What do they bind? What are the markers and chains required for signal transduction? Are they MHC restricted? What do they produce?

A

γδ T cells: These cells use γ and δ chains (instead of α and β chains); they develop in the thymus and have limited diversity; they can bind lipids and heat shock proteins; they are not associated with CD4 or CD8, but do require CD3 and the zeta chain for signal transduction; they do not recognize MHCassociated peptides and are not MHC-restricted; produce IFNy and TNF.

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14
Q

What cells do NK cells kill? How do they know to kill them?

A

They kill viral-infected cells and tumor cells (due to these cells losing MHCI and gaining danger receptors).

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15
Q

What cytokine is important for NK cell development?

A

IL-15

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16
Q

What are markers on NK cells?

A

Markers include: CD16+ (FCRIII), CD56+ (NCAM), natural cytotoxicity receptors (NCRs), and killer inhibitory receptors (KIRs); do not express CD3.

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17
Q

What is NK cell killing mediated via?

A

NK cell killing is mediated via perforin, granzymes, serglycine, and Fas.

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18
Q

What do EBV-infected cells express to activate NK cells? What receptor does this bind on the NK cell?

A

EBV-infected cell expresses CD48 -> binds 2B4 receptor on NK cell

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19
Q

What do stressed cells express that activate NK cells? What do they bind on NK cells?

A

Stressed cell expresses MICA/B, ULBP -> binds NKG2D on NK cell

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20
Q

What do viral hemagglutinin bind to on NK cells? Does this activate or inhibit NK cells?

A

Viral hemagglutinin on target cell -> binds NKp44/46 on NK cell

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21
Q

What does HLA-E bind to to activate NK cells? What does it bind to to inhibit NK cells?

A

Activation: HLA-E -> binds NKG2C on NK cell

Inhibition: HLA-E -> binds NKG2A/B

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22
Q

What do IgG-bound target cells bind to on NK cells? Does this activate or inhibit them?

A

IgG-bound target cell -> binds FcyRIIIA on NK cell (ADCC)

Activates killing

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23
Q

Which cytokines induce development of Th17 cells?

A

IL-6, TGFβ, IL-1, IL-21, and IL-23

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24
Q

How are B and T cells segregrated in the lymph? WHat do they bind to cause this segregration?

A

Anatomic segregation of B and T cells:

  • T-cell zone (parafollicular zone) -> T cell expresses CCR7, which binds CCL19/21 in the T cell/parafollicular zone (as the concentration/gradient of CCL19/21 is highest there).
  • B-cell zone (follicles) -> B cell expresses CXCR5, which binds CXCL13 in the B-cell zone/follicles (as the concentration/gradient of CXCL13 is highest there).
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25
Q

What cytokine is present in high levels during early maturation of B and T lymphocytes? What is deficiency of this cytokine associated with?

A

Maturation of B and T lymphocytes is characterized early on by high levels of IL7 (lack of this cytokine can lead to X-Linked severe combined immunodeficiency disease [SCID])

26
Q

What does positive selection insure during maturation of T cells?

A

That an individual’s T cells can respond to peptides bound to his/her own MHC molecules.

27
Q

What sequences do VDJ recombinase recognize? Where are these sequences located?

A

It recognizes DNA sequences called recombination signal sequences (RSS); recombination occurs between two gene segments (immunoglobulin or TCR) only if one of the segments is flanked by one 12-nucleotide spacer and by one 23-nucleotide spacer -> 12/23 rule.

28
Q

In what cells is RAG1/RAG2 expressed? What does it do?

A

Expressed in immature lymphocytes (i.e., when antigen receptors are being assembled); cleaves double-stranded DNA between the coding segment and its recombination signal sequence.

29
Q

What does Ku do?

A

Binds DNA ends (hairpin in the case of the coding segment)

30
Q

What do DNA-PK (DNA-dependent protein kinase complex) and Artemis do?

A

Open DNA hairpin at a random site

31
Q

What does terminal deoxynucleotidyl transferase (TdT) do?

A

Adds nucleotides for junctional diversity (creates the greatest variability for diversity)

32
Q

What does endonuclease do?

A

Removes nucleotides for junctional diversity.

33
Q

What does DNA ligase IV:XRCC4 do?

A

Ligates DNA

34
Q

What markers are present in the pro B cell stage? What rearrangement occurs during this stage?

A

CD 19+, CD20+; Heavychain D-J then V-DJ rearrange ment

35
Q

What is produced in the pre B cell stage? What signalling and rearrangement occur?

A

Cytoplasmic µ chain produced here; signaling through pre-B–cell receptor and then light-chain V-J rearrangement.

36
Q

What occurs in the immature naive B cell stage?

A

Light-chain product (κ or λ) binds μ heavy chain to make IgM; receptor editing occurs

37
Q

What chains are expressed in the mature naive B cell? Via what process? What is expressed on the cell surface?

A

Express δ heavy chain (as well as μ) via alternative splicing so that IgM and IgD are expressed on the cell surface

38
Q

What occurs during the memory B cell and plasma cell stages? What type of mutations?

A

Memory cell: Isotype switch and somatic hypermutation occurs
Plasma cell: Alternative splicing yields membrane and secreted Ig
Flash

39
Q

At which stage does signaling through the pre-B–cell receptor occur?

A

Pre B Cell

40
Q

What does alternative splicing yield?

A

membrane versus secretory Ig

41
Q

What does differential splicing produce?

A

Differential splicing produces different immunoglobulin isotypes. IgD is the only Ig without a switch region; so, class switching will never apply to it

42
Q

What molecules, if absent, will not allow class switching? What disease occurs?

A
o AID, UNG, CD40, CD40L 
-> if lacking, cannot class switch -> Ig gets ‘stuck’ at IgM -> Hyper IgM phenotype ensues.
43
Q

What transcription factors are associated with commitment to the B cell?

A

Transcription Factors associated with commitment to the B cell include: PU.1, IKAROS, E2A, EBF, PAX5, and IRF8.

44
Q

What signals does B cell survival in the periphery depend on?

A

B-cell survival in the periphery depends on survival signals such as BLYSS, BAFF, and APRIL.

45
Q

What are the receptors on B cell for BLYSS, BAFF, and APRIL? Absence of which one is a risk factor for what disease?

A

BR3 and TACI (early on) and BCMA (later on). No TACI -> CVID risk factor

46
Q

What are the 3 types of mature B cells?

A

B1 cells, Marginal zone B cells, and B2 cells (conventional B cells or follicular B cells).

47
Q

What immune system are B1 cells categorized in? How much diversity is there? What cells are they analagous to? What percent of total B lymphocytes do they make up? What do they produce? What do they respond to? Where are they found? Are they T cell dependent?

A

Innate; limited diversity; analogous to γδ cells; make up 5–10% of total B lymphocytes; self-renewing; produce natural antibodies (low-affinity polyreactive immunoglobulins) that respond to microbes and lipids; found in peritoneal cavity and fetus; T-cell-independent.

48
Q

When are marginal zone B cells developed by? How quickly do they respond to antigens? Are they T cell dependent?

A

Developed by 2 years of age (which explains why infants have poor polysaccharide responses); first responders (especially to polysaccharide antigens); T–cell-independent.

49
Q

What cell types are included in B2 cells? What category of the immune system to they fall into? What do they respond to? Are they T cell dependent?

A

B2 cells (conventional B cells or follicular B cells): includes memory B cells and plasma cells; adaptive; respond to protein antigens; T–cell-dependent.

50
Q

Where are immature T cells located? What do they express? Where do they go when they undergo positive selection? Where do they go when they undergo negative selection?

A

When T cells are immature (DN; CD4–/CD8–), they are located in the subcapsular cortex. As they undergo positive selection, they move to the cortex. As they undergo negative selection, they move to the medulla.

51
Q

How do T cells leave lymphoid organs? What do they do next? What types of cells do they form?

A

T cells leave lymphoid organs by expressing sphingosine-1-phosphate (S1P) receptors. They undergo activation, expansion, and differentiation. Then memory or effector T cells form central memory T cells or effector memory T cells.

52
Q

What are the markers on central memory T cells and effector memory T cells.

A

Central memory T cells: CD45RA–, CD27+, CCR7+, CD62L+ (Lselectin).

Effector memory T cells: CD45RA–, CD27–, CCR7–, CD62L– (Lselectin)

53
Q

Expression of what molecule commits T cells to develop?

A

Notch

54
Q

Do double negative T cells express the TCR? What are the stages of DN T cell? What happens at each stage, and what B cell stage is it analagous to?

A

Does not express T-cell receptor; stages: DN1, DN2 (β chain D-J then V-DJ rearranges; analogous to pro B cell), DN3 (signaling through pre-T–cell receptor; analogous to pre B cell), and DN4 (proliferation)

55
Q

What happens during the double positive stage of T cell maturation?

A

CD4+/CD8+; positive and negative selection occurs; α chain V-J rearranges

56
Q

What do single-positive thymocytes undergo? And what do they become?

A

Cells undergo selection to become CD4+ or CD8+

57
Q

Where does negative selection occur for T cells?

A

The medulla, which is also where the AIRE protein functions

58
Q

What are the two types of lymphocyte apoptosis?

A

Passive/intrinsic and active/extrinsic.

59
Q

What occurs in passive/intrinsic lymphocyte apoptosis? What pathways does it occur via? What is it mediated by?

A

Programmed death by neglect; mitochondrial pathways; mediated by caspase 9; bcl-2 and bcl-XL (antiapoptotic); bid/bim (proapoptotic).

60
Q

What are the steps of the active/extrinsic pathway of lymphocyte apoptosis? What is it mediated by?

A

Repeated lymphocyte activation causes increased Fas (CD95)/FasL(CD178) expression, which causes increased Fas-associated protein with Death Domain (FADD); mediated by caspase 8.

61
Q

What do both types of lymphocyte pathways converge on?

A

caspase 3

62
Q

What are the most common mutations seen in autoimmune lymphoproliferative syndrome (ALPS)? What does this result in?

A

Mutations in Fas(CD95) are the most common defect seen in autoimmune lymphoproliferative syndrome (ALPS), which results in defective lymphocyte apoptosis.