Quiz #2 Flashcards
How do B cells mature?
HSC>CLP> B cell precursor (Ig-) >immature B cell(IgM+) > mature B cell (IgM+/IgD+)
How do B cells go under negative selection?
Any BCR that recognizes self antigen is detected
Avoids self reactive B cells in the circulation
Describe the structure of a BCR?
BCR has two heavy chains, two light chains, and the binding sites are composed of Variable regions, and constant regions
Within the variable region is a hypervariable region
What are the 2 signals that B cells need for activation? What is the third signal?
- Antigen recognition: Ag binds to the Vh and the VL of the BCR, cross linking occurs and Clusters of Iga/B form– results in intracellular signalling
- B cell processes antigen and displays it on MCHII molecules - Costimulation: TCR binds to MHCII peptide and CD40L on T cell binds to CD40 on B cell (1+2= proliferation and effector function)
- T cell cytokines: influence WHICH antibodies are made
How does T cell independent B cell activation occur?
- Triggered by highly repetitive antigens and extensive cross-linking of the BCR to get a strong signal, partial activation,
- Leads to some Ab production, no class switching, no memory
What is the function of an antibody?
neutralization, opsonization and complement activation, increasing phagocytosis through opsonization and mast cells
IgM properties?
can neutralize pathogens, activate complement, opsonize through complement activation, located in blood
IgG properties?
can neutralize pathogens, activate complement, opsonize pathogens, located in blood
IgA properties?
IgA: can neutralize pathogens, located in bodily secretions
IgE properties?
can activate mast cells, located in the tissues
What is neutralization?
Neutralization: antibodies bind the pathogen/toxin and block their interaction with the host
Pathogens and toxins have to bind the host cell to cause disease
What is opsonization?
Opsonization: antibodies bind to the pathogen with their variable region, and the constant region binds to the macrophage through the FcR
Function of proteins in complement?
C3 breaks down into:
C3a: acts as a chemoattractant to bring out more neutrophils
C3b: sticks to surface of bacterium, leads to formation of C5 convertase
C5a: acts as chemoattractants to bring in more neutrophils
C5b: sticks to surface of the bacterium to trigger MAC formation for lysis
Stages of an extracellular bacterial infection? (humoral immunity)
- Tissue damage is a danger signal to activate mast cell degranulation
Leads to the characteristic signs of inflammation - Macrophages activate by PRR recognition (phagocytic and TLRs) of bac PAMP
- Alternative activation of complement cascade
- Macrophages release IL-1, IL-6 and TNFa and CXCL8 - DC phagocytosis bacteria and migrates to the lymph node to present the peptide to the T cell (could also travel through the lymph node on its own)
stages of an Intracellular bacterial infection: (cell-mediated immunity)?
- Have strategies for escaping phagocytosis, like thriving in an acidic environment in the lysosome and then escaping
1. Resident macrophages produce alarm cytokines (IL-1, Il-6 and TNFa) and DC brings antigen to the lymph nodes to show the T cell, T cell makes IFNy
2. IFNy from the Th cell goes to the mac and it produces more protons for acidification, nitric oxide, oxygen radicals and hydrogen peroxide, proteases and defensins (hyperactivation of macrophages) - B cells are less important for an intracellular bacteria because antibodies cant get through the plasma membrane