L6: B-Cells / Humoral Immunity Flashcards
Discuss two types of antibody responses
- ) Primary immune response: occurs 7-10 days after first infection, smaller peak response, antibody isotype primarily IgM, lower antibody affinity, induced by all immunogens
- ) 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
Discuss B cell maturation in terms of DNA, Ig expression, anatomic site and response to antigen
- ) Stem cell: no Ig expression, bone marrow, no response to antigen
- ) Pre-B cell: expresses cytoplasmic mu and pre-B receptor-associated mu, bone marrow, no response to antigen
- ) Immature B cell: membrane IgM expressed (no IgD), released from bone marrow into periphery, undergoes negative selection and receptor editing in response to antigen
- ) Mature B cell: membrane IgM and IgD seen, in periphery, undergoes activation (proliferation and differentiation) in response to antigen
After activation of a mature B cell, what are its options?
- ) Differentiate into a plasma cell
- ) Undergo isotype switching
- ) Undergo affinity maturation
- ) Differentiate into a memory B cell
Mature B cells express IgM and IgD. What are the specificities of each of these Igs?
- Specificity for same antigen/epitope
Discuss how B and T-cells interact? How is this process advantageous? Result?
- 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
Why are B cells less efficient at processing antigen?
- Fewer lysosomes
Outcomes of antibody release by B cell
- ) neutralization of microbes and toxins
- ) opsonization and phagocytosis of microbes
- ) ADCC (NK cells)
- ) Complement activation (phagocytosis of microbes opsonized with complement fragments, inflammation, lysis of microbes)
Distinguish and differentiate between TD and TI antigens that bind B cells
- ) 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
- ) 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
How is signal transduction for B cells made possible as their plasma membrane bound Igs have short cytoplasmic tails?
- They require Ig-alpha / Ig-beta heterodimer
Genes that make up heavy chain of antibody? Light chain?
- 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
What mechanisms account for vast diversity of immunoglobulins?
- ) Pairing of heavy and light chains
- ) Combinatorial diversity: different gene segments rearranged via recombinases (RAG1/2), heavy chain first then light chain genes
- ) Junctional diversity: NT addition / removal occurs at joints between gene segments via TdT
- ) Somatic mutation: point mutations in variable regions of heavy and light chain gene segments
SCID results from deficiency in what genes?
- RAG1 and RAG2 genes
Describe Ig gene rearrangement
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
What is allelic exclusion?
- 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
Naïve B Cells express IgM and IgD that are specific for same antigens. Explain how this occurs from a molecular standpoint.
- 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