Title: Germinal Center Response
1Germinal Center Response
2Hypermutation and selection
- Affinity of Serum Ig increases during an immune
response - Somatic mutation in Ig V region genes, in
response to protein, in B cells in mouse spleen
does not start until after the onset of Ab
production - 2. Mutational process occurs in centroblasts--gt
centrocytes are selected on basis of their
capacity for activation by antigen held on FDCs
3The Germinal Center Reaction
B cells being tested for antibody affinity
Light zone
Antigen-retaining FDCs
Macrophage capturing dead B cells
Dark zone
Rapidly dividing and mutating B cells deep in the
center
4Memory cell
plasmablast
CD40L
Apical light zone
plasmablast
Interaction w/Ag.
?
Basal light zone
Outer zone
No interact. W/Ag.
Death by apoptosis
?
Dark zone
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8Migration of plasma cells
9Immunological Memory
- Four distinct phases
- 1. Induction of B cell memory
- GC reaction
- 2. Maintenance of a B cell memory compartment
- Non-secreting precursor to the memory response
-
- 3. Expression of B cell memory on re-challenge
- 4. Replenishment of the memory compartment
10Summary of B-cell Development in Periphery
11Major Events of Development and Maturation for T-
and B-cells Are Similar
12T-cell Development Occurs In the Thymus While
B-cell Development Is in Bone Marrow
13Thymic Stroma Provides A Unique Microenvironment
for T-cell Development
Thymic Stroma A network of epithelia
cells Analogous to the bone marrow stromal
cells that are required for B-cell development.
14Experimental Data Demonstrating the Critical Role
of the Thymic Stroma in T-cell Development
Scid (severe combined Immunodeficiency) mice
defect in antigen-receptor gene
rearrangement Nude (hairless) mice defect in
whn transcription factor required for
the differentiation of epithelial cells
including thymic epithelial cells
15Major Stages of T-cell Development
CD4-8-
16Figure 7-13
Cell Surface Markers of T-cell Development
17Process Gene Rearrangement Cell
Rearrangement of TCR Genes Is an important
indicator of T cell development
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19Selections and T-cell Maturation
20Co-receptor Specificity of T-cell Is Determined
by the Types of MHC that the TCR interacts with
21Positive Selection Is Mediated by Thymic Cortical
Epithelial Cells
22While the Positive Selection Is Mediated by
Thymic Cortical Epithelia Cells, the Negative
Selection Is Largely Mediated by Bone
Marrow-derived APCs
Via positive and negative selections, mature T
cells acquire the ability to generate effector
mechanisms that serve to eliminate foreign but
not self antigens. Thus, peptides bound to MHC
determine final T-cell receptor repertoire.
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24Bim Plays an Important Role in Negative Selection
of Lymphocytes
25Signaling via TCR Is Required for T-cell
Maturation and Survival
26The Traffic of Lymphocytes Is Controlled by
Chemokines
27Summary of T-cell Development in Thymus
28Summary of T-cell Development in Periphery
29Outline of T-cell Development and Maturation
Abbas
30The ?/? Lineage is Distinct from the ?/? Lineage
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33Experiment showing education of T cells by Thymic
Epithelium
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36Humoral Immune Response
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38Figure 9-1 part 2 of 2
39Two types of antigen, thymus-dependent (T-dependen
t) and thymus-independent (T- independent)
40Thymus dependent antigenAntibody response
requires 2nd signal from T cellMHC class
II/peptide-TCR activates T cells --gt expression
of CD40L on T cell. CD40L interaction with CD40
on the B cell is the second signal
41The same CD4 T cells (Thelper TH) that recognize
peptide-MHC class II, stimulate the B cells
that recognize the same Ag through The BCR
42Thymus independent antigenCan get second signal
from TOLL receptor or cytokine signaling.
Usually the antigen is polymeric
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45Activation of TH cell by MHC class II peptide
induces Expression of CD40L and cytokines, that
activate B cells
46Meeting of antigen-binding B and T cells at the
border Between the T-cell and B cell zones in the
spleen
47Production of a germinal center
48Lymphocytes circulate continually from the blood
into the peripheral Lymphoid tissues, they enter
by squeezing between the specialized endothelial
cells that appear to be larger than those found
elsewhere in the body--gtHigh Endothelial venules
(HEV).