L6: B-Cells / Humoral Immunity Flashcards

1
Q

Discuss two types of antibody responses

A
  1. ) Primary immune response: occurs 7-10 days after first infection, smaller peak response, antibody isotype primarily IgM, lower antibody affinity, induced by all immunogens
  2. ) Secondary immune response: occurs 2-3 days after repeat infection, larger peak, antibody isotype shows relative increase in IgG in comparison to first response, but IgA and E also seen in certain situations, higher antibody affinity as affinity maturation has occurred, induced by mainly protein antigens
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2
Q

Discuss B cell maturation in terms of DNA, Ig expression, anatomic site and response to antigen

A
  1. ) Stem cell: no Ig expression, bone marrow, no response to antigen
  2. ) Pre-B cell: expresses cytoplasmic mu and pre-B receptor-associated mu, bone marrow, no response to antigen
  3. ) Immature B cell: membrane IgM expressed (no IgD), released from bone marrow into periphery, undergoes negative selection and receptor editing in response to antigen
  4. ) Mature B cell: membrane IgM and IgD seen, in periphery, undergoes activation (proliferation and differentiation) in response to antigen
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3
Q

After activation of a mature B cell, what are its options?

A
  1. ) Differentiate into a plasma cell
  2. ) Undergo isotype switching
  3. ) Undergo affinity maturation
  4. ) Differentiate into a memory B cell
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4
Q

Mature B cells express IgM and IgD. What are the specificities of each of these Igs?

A
  • Specificity for same antigen/epitope
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5
Q

Discuss how B and T-cells interact? How is this process advantageous? Result?

A
  • B-cells bind epitope of microbial antigen using their BCR and internalize antigen via receptor-mediated endocytosis
  • Antigen is processed and presented onto class II MHC
  • B-cell presents processed antigen in MHC II to CD4+ T-cell’s TCR. B cell’s B7 interacts with T-cell’s CD28, B cell’s CD40 binds T-cell’s CD40L
  • Result: T-cell releases cytokines, B-cell is activated and differentiates into a plasma cell. If T-cell wasn’t active, it will also now be.
  • The part of the antigen that the T-cell sees is likely different to what the B-cell saw
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6
Q

Why are B cells less efficient at processing antigen?

A
  • Fewer lysosomes
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7
Q

Outcomes of antibody release by B cell

A
  1. ) neutralization of microbes and toxins
  2. ) opsonization and phagocytosis of microbes
  3. ) ADCC (NK cells)
  4. ) Complement activation (phagocytosis of microbes opsonized with complement fragments, inflammation, lysis of microbes)
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8
Q

Distinguish and differentiate between TD and TI antigens that bind B cells

A
  1. ) TD antigens are protein antigens that are thymus-dependenent, in other words, are TH cell dependent. These bind B cell Ig receptors. Activation of B cells with TD antigens allows isotype switching, high affinity maturation, plasma cell differentiation, memory B cell differentiation
  2. ) TI antigens are polysaccharides, nucleic acids and lipids that are thymus-independent, in other words, are TH cell independent. These antigens provide all necessary B cell signals to activate them. Activation of B cells with TI antigens prevents B cells from isotype switching, undergoing high affinity maturation, differentiating into memory B cells
    a. ) TI-1 antigens: bind non-Ig receptors, such as TLR4 (LPS)
    b. ) TI-2 antigens: bind B cell Ig, such as polysaccharide antigens with repeated epitopes
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9
Q

How is signal transduction for B cells made possible as their plasma membrane bound Igs have short cytoplasmic tails?

A
  • They require Ig-alpha / Ig-beta heterodimer
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10
Q

Genes that make up heavy chain of antibody? Light chain?

A
  • V(ariable), D(iversity), J(oining) and C(onstant) genes make up heavy chain
  • V, J and C genes make up light chain. There are kappa and lambda chain loci for each of these genes on different chromosomes
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11
Q

What mechanisms account for vast diversity of immunoglobulins?

A
  1. ) Pairing of heavy and light chains
  2. ) Combinatorial diversity: different gene segments rearranged via recombinases (RAG1/2), heavy chain first then light chain genes
  3. ) Junctional diversity: NT addition / removal occurs at joints between gene segments via TdT
  4. ) Somatic mutation: point mutations in variable regions of heavy and light chain gene segments
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12
Q

SCID results from deficiency in what genes?

A
  • RAG1 and RAG2 genes
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13
Q

Describe Ig gene rearrangement

A

Heavy chain:
- Random D and J segments are brought together, intervening sequences are deleted
- V gene segment randomly selected and placed 5’ to DJ segment to form VDJ segment. VDJ and C region gene separated by intron
- Introns removed during RNA processing
Light chain:
- Random V and J segments are brought together, intervening sequences are deleted. VJ and C region gene separated by intron
- Introns removed during RNA processing

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14
Q

What is allelic exclusion?

A
  • We inherit two sets of heavy chain genes, four sets of light chain genes (2 lambda and 2 kappa)
  • If rearrangement of 1st heavy chain gene set is non-productive, heavy chain genes from 2nd heavy chain gene set is attempted. Allelic exclusion refers successful rearrangement of 1st set of genes.
  • Same thing occurs with light chains with exception that there can be a total of 4 attempts at rearrangement
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15
Q

Naïve B Cells express IgM and IgD that are specific for same antigens. Explain how this occurs from a molecular standpoint.

A
  • Primary RNA transcript contains VDJ region coupled to both constant-mu and constant-delta genes
  • Alternative mRNA splicing encodes IgM and IgD, but VDJ region used is the same
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16
Q

What is the molecular determinant of membrane vs secreted antibody?

A
  • Primary RNA transcript codes for membrane-anchored and secreted forms. If secreted form is required, alternative splicing removes membrane-anchoring sequence from the heavy chain
17
Q

Molecular mechanisms that account for isotype switching

A
  1. ) Long primary RNA transcript containing VDJ region and many/all of constant regions. Alternative splicing sets constant region
  2. ) Deletion of intervening constant region genes (DNA) to align VDJ regions with new constant gene region
18
Q

What cytokines determine isotype switching to IgG, IgE and IgA?

A
  • IgG (1 and 3): IFN-gamma
  • IgE, IgG4: IL-4
  • IgA: TGF-beta, APRIL, BAFF
19
Q

What is affinity maturation? Describe the process

A
  • Affinity maturation refers to process that creates higher affinity antibodies in secondary immune responses in comparison to the primary immune response
    Process: (called somatic hypermutation)
  • VDJ regions are allowed to accumulate point mutations. Activation-induced deaminase aids this process
  • Highest affinity antibodies are selected for by virtue of increased ability to bind antigen and be stimulated by Tfh cells. Inability to do so leads cells to apoptosis.