Properties and Overview of Immune Responses با نام و ياد خدا Antigens E. Salehi Tel: 66419536 Email: eislahi@sina.tums.ac.ir -1تعاريف -2ويژگي هاي آنتي ژنها -3انواع آنتي ژنها -4اپي تپ و انواع آن -5انواع آنتي ژنها ازنظرمنشاء -6عوامل مواثربرايمونوژنسيته -7الگوهاي مولكولي و پذيرنده هاي آن Definitions • • • • • • • • • Immunogen Antigen (Ag) Tolergen Allergen Epitope or Antigenic Determinant Hapten Carrier Super-Antigen Adjuant Characters of Antigen • Degree of “foreignness”-Based on genetic relatedness • Molecular Size-Usually MW >100,000; immunogenic MW <10,000 non immunogenic MW 10,000-100,000 is imunogenically variable Characters of Antigen • Chemical composition-Proteins; Primary, secondary, tertiary and quaternary structure all contribute. • Ability to be processed by APCsFunction of size Chemical Nature of Immunogens • Proteins • Polysaccharides • Nucleic Acids • Lipids – Some glycolipids and phosopholipids can be immunogenic for T cells and illicit a cell mediated immune response Epitopes • In protein antigens epitopes can be defined in terms of: – Amino acid composition – Protein location – Length (5-15 amino acids) • epitopes: • Immunodominant – Epitopes bound by a greater proportion of antibodies than others in a normal in vivo immune response – Also known as Major Antigenic Sites • Sequestered • Epitopes can be divided into 2 classes: – Discontinuous epitopes – Continuous (linear) epitopes Antigenic valence: Total number of determinant which can be combined with Ab. Epitopes could be contiguous (when Ab binds to a contiguous sequence of amino acids) non-contiguous (when Ab binds to non-contiguous residues, brought together by folding). Sequential epitopes are contiguous epitopes. Conformational epitopes are noncontiguous antigenic determinants. Discontinuous Epitopes • Constitutive residues are non-sequential in the primary sequence. • Highly conformational dependant. • Account for approx. 90% of epitopes on a given antigenic (globular) protein. Linear (continuous) Epitopes • Constitutive residues are sequential in the primary sequence of the protein. • Fewer conformational constraints on Ab recognition. • Often contain residues that are not implicated in antibody interaction. Epitopes Sequential Conformational Ab-binding sites Types of Epitopes • Conformational / Discontinuous epitopes: • recognized by B cells • non-linear discrete amino acid sequences, come together due to folding. • Sequential / Continuous epitopes: • recognized by T cells & B cells • linear peptide fragments Types of Peptide Epitope Conformational Antibody or “B cell” Epitope Epitope LinearB cell Epitope Non-Conformational T cell Epitope Class I MHCs Class II MHCs all cells Professional Antigen Presenting cells Foreign and self proteins Foreign proteins 8-10 amino acids 8-20 amino acids T cells and B cells use Distinct Antigen Receptors to Recognize Fundamentally Different Forms of Antigen B cells can recognize linear or conformational epitopes on cell surfaces carbohydrates or of lipids. The B cell antigen receptor is a form of mem T cells recognize linear peptide fragments bound to MHC class I or clas Sperm whale myoglobin (1vxg) contains five sequential epitopes (red, green, magenta, blue, orange) and two conformational epitopes (yellow, pink). كاربرد شناسايي اپي تپ ها Properties of Epitopes • They occur on the surface of the protein and are more flexible than the rest of the protein. • They have high degree of exposure to the solvent. • The amino acids making the epitope are usually charged and hydrophilic. Antigenic Determinants Recognized by B cells and Ab • Composition – Proteins, polysaccharides, nucleic acids – Sequence (linear) determinants – Conformational determinants • Size – 4-8 residues Antigenic Determinants Recognized by B cells and Ab • Composition • Size • Number – Limited (immunodomin ant epitopes) – Located on the external surfaces of the Ag Antigenic Determinants Recognized by T cells • Composition – Proteins (some lipids) – Sequestered determinants • Processed • MHC presentation (lipid presentation by MHC-like CD1) • Size – 8 -15 residues • Number – Limited to those that can bind to MHC Types of Antigens • T-cell independent antigens-Does not require T cell involvement; polysaccharides • T-cell dependent antigens-Requires T cell involvement; proteins Types of Antigens T-independent • Polysaccharides • Properties – Polymeric structure – Polyclonal B cell activation • Yes -Type 1 (TI-1) • No - Type 2 (TI-2) – Resistance to degradation • Examples – Pneumococcal polysaccharide, lipopolysaccharide – Flagella Types of Antigens T-dependent • Proteins • Structure • Examples – Microbial proteins – Non-self or Alteredself proteins Hapten-carrier conjugates • Definition • Structure – native determinants – haptenic determinants Haptenic determinants Native determinants Superantigens • Definition Conventional Antigen Monoclonal/Oligoclonal T cell response 1:104 - 1:105 Superantigen Polyclonal T cell response 1:4 - 1:10 Superantigens • Definition • Examples – Staphylococcal enterotoxins – Staphylococcal toxic shock toxin – Staphylococcal exfoliating toxin – Streptococcal pyrogenic exotoxins • T cell SAg: exotoxin, protein of reverse translate virus • B cell SAg: SPA(staphylococcal protein A) HIV:gp120 Types of Antigens regading the source of Antigen 1. Alloantigens-”same species” ---- ABO blood type, HLA, et al. 2. Heteroantigens-”different species” 3. Xeno-substances ---- Various pathogens and their products,xeno- proteins, etc. 4. Autoantigens- Self component Release of sequestered antigenSuch as lens protein,sperm etc. Change of molecular structure of autotissues Degeneration of protein Forbidden clone rejuvenate 5. Heterophile Ag (forssman Ag) - common Ags shared by different species no specificity of species significance immunopathology & Diagnosis Tumor antigen • Tumor specific Ag, TSA --only express on the tumor cells but normal cells • Tumor associated Ag,TAA --Its express is high on tumor cells but low on normal cells,eg. AFP CEA Factors influencing immune response of Ag Antigen Properties 1.Foreigness 2.Chemical properties of Ag Chemical nature Proteins>Polysaccharides >Nucleic Acids >Lipids Factors influencing immune response of Ag Antigen Properties 3.Molecule weight (size) reasonable large molecule( >10.0 kd) has good immuogenecity. – more stationary – more surface structure for lymphocyte to recognize Factors influencing immune response of Ag Antigen Properties 4. Complexity of Ag structure ring > linear aromatic ring Factors influencing immune response of Ag Antigen Properties 5. Conformation and accessibility 6. Physical states : Polymer > monomer Particulate > Soluble Denatured > Native 7.Degradability – Ag processing by Ag Presenting Cells (APC) Factors influencing immune response of Ag Body Factors Genetics, Species:MHC Individual :Age, health, etc. Factors influencing immune response of Ag Method of Administration Dose Route Subcutaneous>Intravenous>Intragastric times Adjuvant – Substances that enhance an immune response to an Ag Biological Influences on Immunogenicity • Adjuvants-Enhance immunogenicity – Potential mechanism Types • • • • • • • Ag persistence Cell signaling or cytokine effect Induction of inflammation Lymphocyte stimulation Change the chemical and physical charactes of Ag Improves the Ag process and presentation ability of macrophages stimulates proliferation of lymphocytes • Biological adjuvant:BCG,LPS • Synthesized adjuvant Freund’s incomplete adjuvant Freund’s complete adjuvant • Chemical adjuvant Alum Cross reaction: • Reaction between the same Ab and different Ag with same similar determiants. Mechanism of cross reaction • Common Ag determinant • Similar structure of Ag determinant • Significance: Because there are some common antigen determinants between different microbes, so the antiserum against one kind of Ag can also react with another Ag and couse a cross reaction . Determinants Recognized by the Innate Immune System • Adaptive Immune System – Discrete Determinants – Reacts with a specific pathogen • Innate Immune System – Broad Molecular Patterns – Reacts with a variety of pathogens Determinants Recognized by the Innate Immune System • PAMPs – Pathogen Associated Molecular Patterns • PRRs – Pattern Recognition Receptors Biological Consequence of Interaction Opsonization; Complement activation PAMP PRR Microbial cell wall components Complement Mannosecontaining carbohydrates Mannose-binding protein Opsonization; Complement activation Polyanions Scavenger receptors TLR-2 (Toll-like receptor 2) Phagocytosis Lipoproteins of Gram + bacteria Yeast cell wall components Macrophage activation; Secretion of inflammatory cytokines Biological Consequence of Interaction PAMP PRR Double stranded RNA TLR-3 Production of interferon (antiviral) LPS TLR-4 (lipopolysaccharid e of Gram – bacteria) Macrophage activation; Secretion of inflammatory cytokines Flagellin (bacterial TLR-5 flagella) Macrophage activation; Secretion of inflammatory cytokines Biological Consequence of Interaction PAMP PRR U-rich single stranded viral RNA TLR-7 Production of interferon (antiviral) CpG containing DNA TLR-9 Macrophage activation; Secretion of inflammatory cytokines