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Bio 328 Immunology B-cell generation, activation, and differentiation
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B CELL DEVELOPMENT
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Experimental tools to characterization of progenitors: 1.Surface antigens. 2.In vitro culture. 3.Stages of V(D)J rearrangement. 4.KO transcription factors. 5.Expression of TF-driven GFP.
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Early pro-B cell Late pro-B cell
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Schooling of B-cells. Central schooling in the bone marow. Clonal deletion Nemazee and Burki (1989) Tieges et al. (1993) In the periphery
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Bonemarrow Spleen Periarteriolar sheet Marginal follicle Immature B cell T1 B cell T2 B cell Mature B cell
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Schooling of B-cells. Central schooling in bone marrow Clonal deletion (Nemazee and Burki, Tieges et al.) Peripheral schooling in spleen Clonal anergy (Goodnow et al.) T3 B cells Clonal deletion (Nemazee and Burki)
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The three major populations of mature B cells.
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Marginal zone B cells.
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B CELL ACTIVATION
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B cell activation: Competency signal (1) and (2) and Proliferation signal (3)
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Foxn1 deficiency
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Adaptive transfer experiments of Miller, Mitchell, and Mitchison (1960s).
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CD40L CD40 LFA-2
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Activation of B cells by crosslinking the BCR
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B-cell Linker Protein Bruton’s tyrosine kinase
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X-linked agammaglobulinemia
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Importance of co-receptor: (1)# receptors needed to activate B cells (2)HEL-C3b construct (3)Anti-CD19 antibodies (4)CD19 -/- mice
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X-linked hyperimmunoglobulinemia M
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CD40L CD40
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Importance of T H cells: (a) Cross-linking CD40 – CD40L triggers signal transduction pathway. (b) B-cell activation with T H membranes (c) anti-CD40 antibodies
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1 o immunization2 o immunization 2 o anti-Hapten Response Comment Hapten (DNP) --- Carrier 1 (BSA)Carrier 1 (BSA --- Hapten (DNP) + Carrier 1 BSA) --- Hapten-Carrier 1 conjugate (DNP-BSA) +++ Hapten-Carrier 1 conjugate (DNP-BSA) Hapten-Carrier 2 conjugate (DNP-BGG) --- Carrier effect Hapten-Carrier 1 conjugate (DNP-BSA) + Carrier 2 (BGG) Hapten-Carrier 2 conjugate (DNP-BGG) +++ Circumvention of carrier effect.
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Primary Response Naïve B-cell Naïve T-cell + Secondary Response Memory B-cell Memory T-cell + Associative or linked recognition
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Centroblasts CXCR5 Centrocytes CXCR4 FDC
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CXCR5 CCR7 CXCL13 (FDC) CCL19 CCL21 (Paracortex) Movement into follicle Movement into paracortex
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Activation-Induced Cytidine Deaminase
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AID is essential for somatic mutations. Muramatsu M. et al. (2000). Cell 102 p560.
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AID is essential for class switching. Muramatsu M. et al. (2000). Cell 102 p560.
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“Origininal Antigenic Sin”
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Regulation of Immune Responsiveness 1. Effect of prior antigen exposure (anamnestic response or tolerance). 2. Antigen-mediated regulation (antigenic competition, antigen concentration). 3. Antibody-mediated suppression. 4. Immune complexes as regulators. 5. Cytokine-mediated regulation: Th1 and Th2 cells. 6. Idiotype network regulation 7. T-cell -mediated suppression. 8. Neuroendocrine regulation.
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The End
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Regulation of Immune Responsiveness 1. Effect of prior antigen exposure (anamnestic response or tolerance). 2. Antigen-mediated regulation (antigenic competition, antigen concentration). 3. Antibody-mediated suppression. 4. Immune complexes as regulators. 5. Cytokine-mediated regulation: Th1 and Th2 cells. 6. Idiotype network regulation 7. T-cell -mediated suppression. 8. Neuroendocrine regulation.
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