this will be covered later in the course and is presented here to provide context to understanding...

Download This will be covered later in the course and is presented here to provide context to understanding isotype switching. It will not to be tested in Exam

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This will be covered later in the course and is presented here to provide context to understanding isotype switching. It will not to be tested in Exam 1 Stages at which Isotype Switching occurs Slide 2 antigen-independent stem cell pre-B cellimmature B cell (IgM +) mature B cell (IgM , IgD +) IgG IgA IgE IgM antigen-dependent isotype switching Slide 3 Does Isotype Switching occur in one B cell? 1.Activated B cell resides in the Germinal Center -some individuals will mature directly into plasma cells 2.Some B cells in the germinal center divide and undergo hypermutation and/or isotype switching 3.After this stage they cannot divide and the higher affinity ones are selected 4.These cells can mature to plasma cells 5.End result: The B cell makes a different antibody isotype but with the same specificity Slide 4 One B-cell : Two BCR? Exception to the one B-cell: One BCR Dogma One is self-reactive Other is pathogen reactive Why would a B-cell want to express two BCRs of this type? The self-reactive BCR can fill a hole in the B cell repertoire - it might be essential to recognize a pathogen even though it reacts with self. Slide 5 Mechanism of Self-tolerance B-cells with BCR that bind strongly to the constituents of surrounding bone marrow tissue are programmed to die - apoptosis Immune Response Pathogens=0 Deficient Immune Response Pathogens>>0 Overactive Immune Response Pathogens=0 Slightly overactive Immune Response Pathogens>0 Slide 6 Mechanism of Self-tolerance Slide 7 Two Types 1) TCR and TCR T cells TCR and TCR T cells Antigen Binding site - V and V Similar to Fab fragment T-cell Receptor Slide 8 T cells - Recognize MHC:peptide complex - Diverse Functions A) Stimulate other immune cells B) Cytotoxic - kill infected host cells - Cell:cell interactions T cells - Dominant T-cell in epithelial tissue (only 1-5% in circulation) - Recognizes more than MHC:peptide - Not well characterized Functions and Properties of T Cells Slide 9 Antigen-Recognition site = Peptide:MHC Recognition site Single V region - CDR1-3 for each chain All TCRs on a single T cell are the same Different T cells express different TCRs Diversity mechanisms like BCRs Slide 10 Figure 3-3 No Ds in V gene DJ first then VDJ in gene rearrangement Occurs in the Thymus Slide 11 Figure 3-8 -chain locus is within -chain locus Fewer V segments then and Two D segments can be incorporated Slide 12 Functional T-cell Receptor Complex Core complex CD3 complex: , (zeta) chain Function of CD3 and : Transport Signal Transduction Invariant Chains Avidity Slide 13 PROPERTYB CELLST CELLS Initial DevelopmentBone MarrowThymus Pre-antigen Diversity YES Post antigen Diversity YESNO Single antigen specificity YES Antigen recognizedVarietyPeptide:MHC Secreted form of Receptor YesNo Invariant signaling subunits Yes Comparison of B and T cells Slide 14 SCID - severe combined immunodeficiency disease - Many causes but a rare disease - Classified according to lymphocyte profile (T B NK) - Bone Marrow transplant can cure Omenn syndrome - RAG proteins have reduced activity - Patient is: T+ B- NK+ CD3 and CD3 deficiency diseases - Mutations in some CD3 genes - Patient is: T+/TCR- B+ NK+ or T- B+ NK+ Immunodeficiency diseases Slide 15 How do T cells recognize antigens? Antigen Processing Antigen Presentation Antigen Presenting Cell (APC) Professional APC Slide 16 MHC class I communicates with Tc cells Slide 17 MHC class II communicates with T H cells Slide 18 IR to Extracellular Pathogens (CD4-MHC I) 1.Antibodies needed 2.Pathogen recognition/internalization by professional APCs a. B cells b. Macrophages c. Dendritic cells 3.Phagolysosome degrades proteins to peptides 4.Peptides:MHC II complex transported to surface 5.Professional APC contacts CD4 T cells 6.CD4 T H cells secrete cytokines to signal B cell maturation Slide 19 IR to Intracellular Pathogens (CD8-MHC II) 1.Antibodies ineffective 2.Pathogen replicates in the cell and proteins are degraded in the cytoplasm of the cell 3.Peptides are transported into ER and bind MHC I and transported to the surface 4.MHC I expressing cells present to CD8 T cells 5.CD8 T cells (cytotoxic T cell, CTL) kills host cell Slide 20 Figure 3-11 Slide 21 Structures involved in MHC Presentation TCR CD4 and CD8 MHC1 and MHCII Slide 22 T cell Co-Receptors Slide 23 Figure 3-13 part 1 of 2 Slide 24 CD8-MHC ICD4-MHC II Slide 25 Figure 3-15 ClosedOpen 8-10 amino acids 13-25 amino acids Degenerate binding specificity Slide 26 Figure 3-16 Slide 27 Proteosome=Shredder Transporter associated with antigen processing Peptide Degradation and Transport Slide 28 Chaperones Slide 29 Slide 30 Figure 3-19 Slide 31 CLIP - class II-associated invariant-chain peptide Prevention of Peptide:MHC II formation in ER Slide 32 Figure 3-21 part 2 of 3 TCR binds MHC and peptide Slide 33 Slide 34 Sample Exam Question Testing allelic exclusion (inherit alleles for each Ig locus; only one rearranges to produce a heavy or light chain) Which of the following best describes the process of allelic exclusion? a. BOTH alleles of the light chain locus (e.g. lambda) rearrange DNA, but only ONE allele of the heavy chain rearranges DNA b. BOTH alleles of the heavy chain locus rearrange DNA, but only ONE allele of the light chain (e.g. lambda) rearranges DNA c. BOTH alleles of the light chain locus and BOTH alleles of the light heavy chain rearranges DNA d. The primary transcript RNA from BOTH alleles of the light chain and BOTH alleles of the heavy chain is rearranged e. None of the above Slide 35 NOT a Sample Exam Question Testing obscure facts that are probably NOT relevant to your education How many Diversity segments (D H ) are present in the Immunoglobulin Heavy chain locus? a. 26 b. 27 c. 3.3 x 10 6 d. It varies depending on the combinations made with the light chain e. None of the above