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Introduction to Immunology. Jianzhu Chen Department of Biology Massachusetts Institute of Technology jchen@mit.edu. Principles of adaptive immunity TCR recognition Antigen presentation and processing Host defense against viruses. Innate. Adaptive. Cells Ag receptors
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Introduction to Immunology Jianzhu Chen Department of Biology Massachusetts Institute of Technology jchen@mit.edu • Principles of adaptive immunity • TCR recognition • Antigen presentation and processing • Host defense against viruses
Innate Adaptive Cells Ag receptors Ag recognition Speed Memory Innate immunity: Preformed, non-specific effectors. Adaptive immunity:Immune mechanisms that are mediated by T and B lymphocytes and that change in response to infection.
Principle of the Adaptive Immunity What is fundamental challenge faced by the immune system? Fact: Strategy: Solution:
What are the consequences of using V(D)J recombination to create antigen receptor diversity?
V V V V a V Key molecules and cells of the adaptive immunity 3 molecules 3 cell types 4 cardinal features Antigen-presenting cells (APC) Dendritic cells (DC) Macrophage B cells B cells T cells
Antigen recognition by BCR and TCR
TCR-peptide-MHC (pMHC) interaction
MHC Structure Wiley et al. 1987 peptide
TCR-pMHC interaction Extensive contacts: between TCR and peptide between TCR and MHC TCR molecules are evolved to bind to MHC
Major Histocompatibility Complex (MHC) 1930s: Peter Gorer identified four groups (I, II, III, and IV) of blood cell antigens in inbred mice. 1950s: George Snell established the group II antigens mediate rejection of transplanted tumors and other tissues. Histocompatibility antigens (H-2 in mouse) Human Leukocyte Antigens (HLA in human)
MHC Restriction MHC type determine the ability of T cell response. Zinkernagel & Doherty, 1975
a MHC Structure Similar to Ig and TCR, belongs to the Ig superfamily
MHC Structure Class I + 2m (2 microglobulin) Class II + subunits peptide peptide 2 1 1 1 Model: 3 2m 2 2 Simplified: Gene: a3 Tm L a1 a2 C C Peptide-binding proteins Peptide is part of the stable structure (heterotrimers)
MHC Structure Class I Class II Peptide binding cleft Peptide binding cleft b2m
MHC Structure Cell MHC Denature Peptide mass spectrometry Peptide Sequence
MHC Nomenclature Mouse H2-K -D -L H2-IA -IE Class I Class II HLA-A -B -C HLA-DP -DQ -DR • Human • Human • Leukocyte • Antigen Example: HLA-A2 (or A2), human MHC class I A molecule, allele 2 Haplotype: each set of alleles • H2-Kd (Kd)IAd • Balb/c H-2dH2-Dd (Dd)IEd • H2-Ld (Ld)
MHC Function DP DQ DR HLA-C HLA-B HLA-A 2b 2a 3b 2a 3b 1a How can a small number of MHC molecules present a large number of peptides for TCR recognition? • Polygenic Possible MHC class I combinations in one individual: 2A + 2B + 2C = 6
MHC Function DP DQ DR HLA-C HLA-B HLA-A 2b 2a 3b 2a 3b 1a 89 19 45 20 350 2 470 110 240 How can a small number of MHC molecules present a large number of peptides for TCR recognition? • Polygenic • Polymorphic Presence of multiple alleles at a given locus within a species Possible MHC class I combinations in the human population: 470 x 110 x 240 = 1,240,800
MHC Function Differences in amino acids are concentrated in the peptide-binding groove. Different MHC molecules bind to different set of peptides How can a small number of MHC molecules present a large number of peptides for TCR recognition? • Polygenic • Polymorphic • Extremely polymorphic • 5% 20 a.a.
MHC Function DP DQ DR HLA-C HLA-B HLA-A 2b 2a 3b 2a 3b 1a 89 19 45 20 350 2 470 110 240 How can a small number of MHC molecules present a large number of peptides for TCR recognition? • Polygenic • Polymorphic • Co-expression • Presentation of multiple peptides per MHC molecule >2,000 peptides per class I molecule >> 2,000 peptides per class II molecule ~105 molecules per cell