13 - B Cell Effector Functions Flashcards

1
Q

Humoral immune response

A

Mediated by antibodies secreted by plasma cells

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2
Q

Signals that induce B cells to proliferate and differentiate into plasma cells

A

Signals from the bound antigen and from helper T cell in the form of CD40L and cytokines

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3
Q

Three main ways antibodies protect the host from infection

A
  • Neutralisation
  • Opsonisation
  • COmplement activation
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4
Q

Signals required for B cell activation

A
  • First signal is delivered through the B cell antigen receptor
  • Second signal is either thymus dependent (TD) or thymus independent (TI)
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5
Q

Thymus dependent antigen second signal

A

Delivered by helper T cells that recognise antigen bound to MHC-2 molecules. (CD40, CD40L is essential part of second signal)

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6
Q

Thymus independent antigen second signal

A

Delivered with antigen, through TLR that recognise antigen associated TLR ligands (e.g. bacterial LPS)

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7
Q

Helper T cells

A

Stimulate proliferation and then differentiation of antigen binding B cells in lymph nodes

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8
Q

Cytokines secreted by T cells in B cell activation

A
  • IL-4, 5 and 6
  • Drive proliferation and differentiation of B cell into antibody secreting plasma cells
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9
Q

Linked recognition

A

B cells and helper T cells must recognised epitopes of the same molecular complex in order to interact

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10
Q

Process of linked recognition

A
  • B cell binds virus through viral coat protein
  • Virus particle is internalised and degraded
  • Peptides from internal proteins of the virus are presented to the T cell, which activated the B cell
  • Activated B cell produces antibody against viral coat protein
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11
Q

Structure of a germinal centre

A
  • A specialised microenvironment in which B cell proliferation and somatic hypermutation occur
  • Composed mainly of proliferating B cells
  • Antigen specific T cells make up ~10% of germinal center lymphocytes
  • Grows in size as immune response proceeds
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12
Q

Germinal center after clearance of infection

A
  • Shrinks and disappears
  • Present for about 3-4 weeks after intial antigen exposure
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13
Q

Centroblasts

A

Rapidly proliferating B cells in dark zone

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14
Q

Centrocytes

A

B cells dividing less frequently in light zone

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15
Q

IL-4

A
  • Produced by CD4+ helper T cells and upregulate CD40L (on T cells)
  • Confined to space between B and T cell after secretion
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16
Q

Helper T cell cytoskeleton and secondary apparatus during B cell activation

A

Reoriented towards the B cells

17
Q

T cell and B cell migration to border between T cell area and B cell follicle in lymphoid tissue

A

Naive CCR7+ T cells and CXCR5+ B cells home to distinct regions where the chemokines CCL21 and CXCR13, respectively,
are produced

18
Q

Subcapsular macrophages

A

The low endocytic and degradative activity of subcapsular macrophages preserves the antigens trapped on their surface, allowing B cells to encounter them

19
Q

Iccosomes

A

immune complexes bound to FDCs form iccosomes which are released and taken up by B cells in germinal centres

20
Q

Activated B cells form germinal centres in lymphoid tissues

A
  • Naive B cells enter the lymph node via HEV and leave via efferent lymphatics
  • B cells that encounter antigen in the follicle form a primary focus, some form a germinal center
  • Plasma cells migrate to the medullary cords or leave via efferent lymphatics
  • Plasma cells migrate to bone marrow
21
Q

Rounds of mutation and selection of activated B cells

A

Mutation and selection for higher affinity mutants in the germinal centre, resulting in high affinity antibody secreting plasma cells and high affinity memory B cells

22
Q

Somatic hypermutation and affinity maturation

A
  • In the germinal centres of a lymph node, the variable regions of BCRs are constantly acquiring mutations
  • Mutations that negatively affect the BCR’s affinity for its antigen will be selected against, while mutations in that positively affect affinity will cause proliferation
23
Q

Processes that germinal center B cells undergo

A
  • Somatic hypermutation
  • Affinity maturation
  • Class switching
24
Q

What antibody isotype do all naive B cells initially express

A

IgM and IgD

25
Q

Which part of antibody is specific for antigen

A

Variable region (must be maintained during recombination events in isotype switching)

26
Q

Recombination events in isotype switching

A
  • Genes encoding the constant region corresponding to each isotype are arranged in a linear fashion
  • During isotype switching, a portion of the DNA is looped out as switch regions recombine
  • After recombination, the constant region directly downstream of the VDJ region will encode the isotype produced on the surface of the B cell and secreted
27
Q

What is class switching controlled by

A

Cytokines

28
Q

Polyclonal activation

A
  • At high concentration, the signal delivered by the TI-1 antigen is sufficient to induce proliferation and antibody secretion by B cells in the absence of specific antigen binding to the surface Ig.
  • Therefore all B cells respond.
29
Q

Another name for TI-1 antigens

A

Mitogens (substance that induces cells to undergo mitosis)

30
Q

Disadvantages of polyclonal antibody responses

A

Pathogens have evolved to induce polyclonal antibody responses so that specific antibody is diluted

31
Q

Multiple cross linking of BCR by TI-2 antigens

A
  • Can lead to IgM production
  • Cytokines (e.g. BAFF secreted by DCs) increase these responses and lead to class switching
32
Q

Infant immunity

A

Capable of mounting adaptive immune responses, but their ability to develop long lasting immunity is limited

33
Q

Hib vaccine

A
  • Against Haemophilus influenzae type b
  • Conjugate of bacterial polysaccharide and the tetanus toxoid protein
34
Q

How does Hib vaccine work

A
  • The B cell recognises and binds the polysaccharide, internalises and degrades the whole conjugate and then displays toxoid-derived peptides on surface MHC Class II molecules
  • Helper T cells generated in response to earlier vaccination against tetanus toxoid recognize the complex on the B cell surface and activate the B cell to produce anti polysaccharide antibody
35
Q

The immune system antibodies against blood types

A

Forms antibodies against whichever ABO blood group antigens are not found on the individual’s RBC’s (e.g. Blood group A have antibodies againts blood group B)