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Mechanisms of Allergic Immunity crah1@le.ac.uk
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Normal larynx Laryngeal oedema
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Cellular culprits of allergy: Mast cells Most informative early analysis conducted in patients with asthma Early studies (pre-1980) implicated mast cells and histamine as part of an archetypal immediate type I hypersensitivity Provoked by allergenic and non allergenic substances Explained atopic and non-atopic asthma Explained why mast cell stabilising drugs worked
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Cellular culprits of allergy: Mast cells?? Corticosteroid treatment worked, but had no effect on histamine release Anti-histamine treatment had little effect on asthma Could not explain ‘organ specificity’ of asthma Could not explain the hyperresponsive airway in asymptomatic asthmatics Fibreoptic bronchoscopy - immunohistology, biopsy and analysis of bronchoalveolar lavage (BAL) cells (1980’s - present)
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The early evidence: Eosinophil & mononuclear cells infiltrate the bronchi of asthmatics Activated T cells elevated in the peripheral blood of severe acute asthmatics Activated T cells in peripheral blood correlated with airway narrowing Bronchial CD4 lymphocyte numbers correlated with eosinophil numbers Elevated IL-5 expressing T cells in asthmatic bronchial mucosa and BAL T cells that release IL-5 co-localise with eosinophils Eosinophils cause airway hyperresponsiveness, inflammation desquamative bronchitis, mucous hypersecretion and smooth muscle contraction IL-5 promotes differentiation and regulates the survival of eosinophils Steroid treatment associated with a decrease in IL-5 producing cells Cellular culprits of allergy: T cells
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Cellular culprits of allergy: T cells Wider analysis of cytokines in atopy showed that BAL T cells that expressed elevated levels of IL-5, also expressed IL-4 - a profile typical of Th2 cells in mice IL-3 Growth of progenitor haemopoeitic cells GM-CSF Myelopoiesis. IL-4 B cell activation and growth IgE isotype switch. Induction of MHC class II. Macrophage inhibition IL-5 Eosinophil growth IL-6 B cell growth Acute phase protein release IL-10 Inhibits macrophage activation Inhibits Th1 cells TGF- Inhibits macrophage activation
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Lebman & Coffman 1988 J Exp Med 168, 853-862
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‘Textbook’ scheme of allergic immunity is centred around polarised Th cells Where do Th2 cells come from? Why are they so dominant in allergic individuals? What are they really for?
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Journal of Immunology 136, 2348-2357 1986 The discovery of Th1 and Th2 subsets
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IL-4 IFN-g T cell clones that make IFN-g, but not IL-4 T cell clones that make IL-4, but not IFN-g Enhances IgE & IgG1 Do not provide help to IgE and IgG1 secreting B cells Provide help to IgE and IgG1 secreting B cells In vitro - Th1 and Th2 subsets
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Relevance in vivo - Infection Non-healing BALB/c Resistant C57BL/6 Draining LN T cells express IL-4 mRNA Draining LN T cells express IFN-g mRNA T Leishmania - specific T cells Irradiated BALB/c recipient Resistance Reiner & Locksley Annu. Rev. Immunol. 13, 151-177, 1995
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IFN- / IL-12 or anti-IL-4 Pro-Th1 treatments or anti-Th2 treatments protect against infection Relevance in vivo - Infection
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Macrophage infected with Leishmania kills pathogen when activated Macrophage activation is dependent upon Th1 cells Leishmania resistance - mechanism
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Tuberculoid leprosy Low infectivity Localised infection Normal serum Ig Normal T cell response Poor growth of mycobacteria in macrophages Th2 Th1 Lepromatous leprosy High infectivity Disseminated infection Hypergammaglobulinaemia Unresponsive Florid growth of mycobacteria in macrophages Relevance of Th subsets in humans Lepromatous and tuberculoid leprosy Infection with Mycobacterium leprae shows two main clinical forms associated with Th1 and Th2 responses
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Tuberculoid leprosy
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Lepromatous Leprosy
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‘Textbook’ scheme of allergic immunity is centred around polarised Th cells Immunological fashions 1960’s & 1970’s Immunoglobulin E 1970’s & 1980’s Mast cells & Eosinophils 1980’s & 1990’s Environment – ante-natal & adult, allergens, Th2 cells 1990’s & 2000’s Microbial experience, Epithelium, Tregs Although undoubtedly a useful model, the textbook ‘skew to Th2’ model is too simplistic to explain allergy Allergy is a disease of impaired immune regulation Where is the regulatory lesion?
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Barrier: Skin, gut, lung, eye, nose etc Non self protein from allergen or pathogen Allergic immune responses are much like any other immune response and involves the same regulators Inflammation inc. MIP-1a, MCP-1 MIP-1b
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Tracheal Dendritic Cells Langerhan’s cells In-vitro differentiated monocyte-derived Dendritic Cell
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[Ca2+]i Time (s) [Ca2+]i Time (s) Immature DC migrate into inflamed tissue in response to MIP-1a, MCP-1 MIP1-b which bind to, and trigger CCR1, CCR2 and CCR5 respectively. Migration of immature DC to sites of inflammation Sallusto et al., Eur. J. Immunol. 1998 28 2760-2769 Immature DC do not respond to the lymph node derived CCR7 ligand MIP-3b Time (s) [Ca2+]i
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Mature DC stop migrating into inflamed tissue and make no response to MIP-1a, MCP-1 MIP1-b Mature DC respond to the lymph node derived CCR7 ligand MIP-3b Time (s) [Ca2+]i Migration of mature DC to 2º lymphoid tissue Sallusto et al., Eur. J. Immunol. 1998 28 2760-2769 Time (s) [Ca2+]i Time (s) [Ca2+]i
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Mempel, T.R et al Nature 427: 154-159, 2004. Splenic DC Pulsed with Ag OVA 323-329 Not pulsed with Ag T cells labelled GREEN Anti OVA 323-329 TcR transgenic mouse DC labelled RED DC – T cell interactions in the lymph node -18hr 0hr 2hr Anti-L selectin Ab Imaging at various timepoints
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2. Distribution of Ag-loaded DCs and T cells is ordered 4-5hr after T cells are injected 1. DCs strategically cluster around HEV 18hr after entering the LN Early entry of DC to the lymph node Mempel, T.R et al Nature 427: 154-159, 2004.
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3. DC become highly migratory & change shape (20hr)
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4. T cells cover large territories in LN
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6. Short, serial T cell-DC contacts of ~ 5 minutes (2-4hrs after injection of T cells) 7. Stable T cell-DC conjugates of 30-180 minutes (8-12hr after injection of T cells) 8. Simultaneous stable and dynamic interactions between DC and T cells
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5. 44hr after injection of T cells, DCs decrease motility and become anchored to reticular fibres, T cells rapidly migrate again T cells start to proliferate and produce cytokines 44hr after transfer
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More information than is provided by the antigen is exchanged between the DC and T cell DC have a profound influence on the properties of the T cell that develops
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Signals 1, 2 Signal 1 antigen & antigen receptor Signal 2 B7 - CD28 Costimulation and 3 Signals 1 & 2 activate T cells to proliferation and effector function But what ‘tunes’ the response to Th1 or Th2?
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Polarised DC subsets DC Th The properties of the allergen, or allergen carrier influences the DC to drive the development of appropriate Th cells Signal 3 Th polarising signal Integration of signals from pathogen/allergen and the extracellular milieu polarise the DC to produce qualitatively different signals 3 Signal 1 Signal 2
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Microbial Patterns Janeway & Medzhitov 2002 Ann Rev Immunol 20 197-216 Pathogen-associated molecular patterns (PAMPS) Conserved microbial molecules shared by many pathogens Include: Bacterial lipopolysaccharides Peptidoglycan Zymosan Flagellin Unmethylated CpG DNA Pattern Recognition Receptors (PRR) Include: Toll like receptors Receptors for apoptotic cells Receptors for opsonins Receptors for coagulation and complement proteins Pathogen-associated molecular patterns (PAMPS) Conserved microbial molecules shared by many pathogens Include: Bacterial lipopolysaccharides Peptidoglycan Zymosan Flagellin Unmethylated CpG DNA
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CD40 + CD80/CD86 Type 1 and 2 DC Polarising PAMPS Type 1 PAMPS bind to PRR Class II Type 2 PAMPS bind to PRR Th1 polarising factor IL-12 Th2 polarising factor CCL2 (MCP-1) T + +
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CD14 TLR 4 MD-2 TLR 3 TLR 9 TLR 2 TLR 1 TLR 6 TLR 2 Type 1 PAMPS and their PRR Peptidoglycan (Gram + bacteria) Lipoproteins Lipoarabinomannan (Mycobacteria) LPS (Leptospira) LPS (Porphyromonas) Glycophosphatylinositol - (T. Cruzi) Zymosan (Yeast) LPS Lipotechoic acid - (Gram + bacteria) RSV F protein dsDNA Unmethylated CpG DNA Low level IL-12p70 Some ligands induce IL-10 or IL-12p35 High IL-12p70 IFN-a High IL-12p70 High IL-12p70 IFN-a
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Type 2 PAMPS and their PRR ? ?
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Endogenous molecular patterns Endogenous molecular patterns Include: Heat shock proteins (HSP60 HSP70 GP96) Extracellular matrix proteins (hyaluronan, fibronectin, fibrinogen) Immune complexes Surfactant protein A Necrotic cell components Pattern Recognition Receptors (PRR) Include: Toll like receptors Receptors for apoptotic cells Receptors for opsonins Receptors for coagulation and complement proteins Receptors for apoptotic cells Receptors for opsonins Receptors for coagulation and complement proteins
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Indirect activation of DC by ‘modulatory tissue factors’ Direct activation by PAMP-PRR interactions Necrotic/apoptotic cell death - neo expression of PRR ligands Heat shock proteins Extracellular matrix components Necrotic cell lipids Cytokines Chemokines Eicosanoids Coagulation components Complement components Allergen Activates the expression of costimulatory molecules on DC
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Could be argued that the development of Th2 cells is the default pathway DC polarisation by modulatory tissue factors DC polarising factors IFN-g IFN-a IFN-b Th0 to Th1 polarising cytokines IL-12p70 IL-27 TNF-b IL-18 DC polarising factors CCL7 (MCP-3), CCL13 (MCP-4), PGE2, Histamine Th0 to Th2 polarising cytokines CCL2 (MCP-1), ?IL-4 Lack of high level IL-12p70 IL-27 TNF-b IL-18
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NK Epithelium Mast Fibroblast PGE2 CCR2L Histamine IFN-g IFN-a IL-18 Viruses Fungi Parasites Bacteria Viruses Viruses Fungi Parasites Viruses Sources of modulatory tissue factors Th2 Th1
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The hygiene hypothesis (Strachan, 1989) Based upon the epidemiology of hay fever “Declining family size, improved household amenities, and higher standards of personal cleanliness have reduced the opportunities for cross-infection in young families. This may have resulted in more widespread clinical expression of atopic disease" ..can be interpreted in terms of a failure to microbially modulate default Th2 responses in childhood young families Explains how Th2 arise, but… …does not explains why some individuals are allergic and others are not and why the incidence of allergy is increasing. Reduced numbers of IL-12 producing cells? Reduced ability to produce or respond to IL-12? Reduced stimulation of IL-12 by microbial substances?
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Th2 Th1 Th2 Balanced Th1/Th2 at ~2yr Neonatal & infant immune systems The intrauterine environment is powerfully Th2 – this imprints Th2 dominance upon the neonate Serial infections Age Immune response
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Th1 Th2 Unbalanced Th1/Th2 Th2 dominance at ~2yr Delayed maturation of Th1 capacity Few serial infections – hygiene, small family size etc Age Immune response Longer period of time in which to make and establish Th2 responses to environmental antigens (i.e. allergens)
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Do infections only reduce Th2 dominance by inducing Th1 responses? Aerosolised ovalbumin (OVA) OVA – allergic mice with asthma-like symptoms Eosinophils in airway, dominance of OVA-specific Th2 cells, OVA-specific IgE Wheeze Vaccinate with mycobacteria No asthma-like symptoms Wheeze Have the Th1 cells induced by the mycobacteria downregulated the activity of the Th2 responsible for the symptoms?
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Vaccinate with mycobacteria Wheeze No asthma-like symptoms Do infections only reduce Th2 dominance by inducing Th1 responses? Th CD4+ cells specific for OVA that produce high levels of the immunosuppressive cytokines TGFb and IL-10 Mycobacteria induced REGULATORY T cells
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Th cell polarisation DC mediated – decision influenced by infection Extracellular milieu - mediated
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0 1 10 Factor increase over control 0 1 10 Factor increase over control Journal of Immunology 1994 152 4755-4782 Priming conditions IFNg U/ml IL-4 pg/ml Control Ab 5892 256 Anti-IFNg Ab 1534 624 IL-4 + control Ab 1740 839 IL-4 + anti-IFNg Ab 348 1245
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Resting Mast cell Degranulated mast cell Mediators released include: Leukotriene C4 & D4, Prostaglandin D2 Platelet Activating Factor, Chymase, Tryptase, Heparin, Histamine IL-4, IL-5, IL-6, IL-8, TNF-a IL-4, IL-5 IL-4 is not only a product of Th2 cells IL-4 from the innate immune system
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Journal of Experimental Medicine, 1992 176 1381-1386 Sequential 2mm sections from a mucosal biopsy of a patient with asthma Tryptase IL-4
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What properties and characteristics make a substance an allergen? How do these properties disregulate the processes described?
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L. destructor G. domesticus D. pteronyssinus D. pteronyssinus A. siro T. putrescentiae
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Allergens of Dermatophagoides pteronyssinus Proteinase allergens are common and widespread: Fungi, insects, plants, parasites, drugs (but…most allergens are not proteases) Der p 1 Cysteine protease Der p 2 ? Der p 3 Trypsin (serine protease) Der p 4 Amylase Der p 5 ? Der p 6 Chymotrypsin (serine protease) Der p 7 ? Der p 8 Glutathione transferase Der p 9 Collagenase (serine protease) Der p 10 Tropomyosin Der p 14 Apolipophorin like protein
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Protease allergens can breach epithelial barriers Wan et al., Der p 1 facilitates transepithelial allergen delivery by disruption of tight junctions J Clin Invest, 1999, 104, 123-133 Leads to immune sensitisation without the ‘deliberate’ invasion and infection mechanisms of a pathogen
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Proteases as activators of cells Protease Activated Receptors PAR Activators Inactivators PAR1 Thrombin, Trypsin Granzyme A Cathepsin G, Elastase, Plasmin Proteinase 3 PAR2 Trypsin, Tryptase, Factor Xa, Proconvertin Cathepsin G,, Plasmin, Proteinase 3 PAR3 Thrombin Cathepsin G, Elastatase PAR4 Thrombin, Trypsin, Cathepsin G ?
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Journal of Immunology 2001 167 1014-1021 PAR are also involved in: Induction of of epithelial cell & fibroblast proliferation Induction of cytokines & chemokine expression Induction of pharmacological mediator release Induction of metalloproteases Regulation of smooth muscle tone
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Resting Mast cell Degranulated mast cell Mediators released include: Leukotriene C4 & D4, Prostaglandin D2 Platelet Activating Factor, Chymase, Tryptase, Heparin, Histamine IL-4, IL-5, IL-6, IL-8, TNF-a IL-4, Do protease allergens induce IL-4 release by Mast cells
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Journal of Leukocyte Biology 2003, 73 165-171
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Constitutive & Induced Cytokine Expression by KU812 Basophils b-actin IL-3 IL-4 IL-5 IL-6 IL-8 IL-13 IFN-g 516bp 516bp Constitutive PMA/Ionomycin Induced
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b-actin 516bp 516bp 516bp 516bp 516bp IL-4 IL-5 IL-13 IFN-g Der p1 Inhibited Der p1 Inhibitors 0 +ve -ve Der p1 Induces Cytokine Type-2 Cytokine mRNA Expression in KU812
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516bp 516bp PMA/Ionomycin Inhibitors - - + + + + - - b-actin IL-13 Protease Inhibitors Do Not Prevent Cytokine mRNA Expression by KU812
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516bp b-actin IL-13 - - - + PMA/Ionomycin Tetanus toxoid - - - + - + -ve 516bp Time (hr) 1 1 4 4 4 Non-Proteolytic Antigens Do Not Induce Cytokine mRNA Expression by KU812
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Der p1 induces IL-4 and IL-13 protein expression in Freshly isolated Basophils
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516bp 516bp 516bp 516bp 516bp b-actin IL-4 IL-5 IL-13 IFN-g - Inhibitors + Inhibitors -ve +ve 0 ES 100ng/ml ES 200ng/ml ES 1000ng/ml ES 0 ES 100ng/ml ES 200ng/ml ES 1000ng/ml ES Necator Americanus Proteases Induce Type-2 Cytokine Expression by KU812
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Der p1 and hookworm excretory/secretory products induce IL-4 and IL-13 protein expression in KU812 Basophils
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The switch to IgE
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Lebman & Coffman 1988 J Exp Med 168, 853-862
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Switch regions The Sm consists of 150 repeats of [(GAGCT)n(GGGGGT)] where n is between 3 and 7. Switching is mechanistically similar to V(D)J recombination. Switch regions - repetitive regions of DNA that physically recombine Upstream of C regions
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Switch recombination to IgE A three signal process: Antigen – controls entire process Soluble help via IL-4 or IL-13 from T helper cells Cognate help via CD40 L from T helper cells
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Y Y Y T cell help to B cells B Antigen Th Th IL-4 and IL-13 CD40 Ligand CD40
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Switch recombination to IgE A three signal process: Antigen Soluble help via IL-4 or IL-13 from T helper cells Cognate help via CD40 L from T helper cells
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Stat-6 P Stat-6 P Soluble help via IL-4 or IL-13 from T helper cells IL-4Ra IL-4Ra gC IL-13Ra1/2 IL-13 IL-4 IL-13 IL-4 IL-4R IL-13R JAK1 JAK3 TYK1 JAK1 TYK2 P P Stat-6 P Stat-6 P P P Stat-6 P P Stat-6 P P Stat-6 P P P Dimerised Stat-6 translocates to nucleus
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Switch recombination to IgE A three signal process: Antigen Soluble help via IL-4 or IL-13 from T helper cells Cognate help via CD40 L from T helper cells
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Ligation promotes aggregation in lipid rafts Cognate help via CD40 L from T helper cells CD40 2 3 5 6 TNF receptor associated factors IkB NF kB IkB NF kB Uninhibited NFkB translocates to the nucleus
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Stat6 Ie Ce1 Ce2 Ce3 Ce4 Se Ie NFkB C/EBP PU.1 BSAP AP-1 BSAP – B cell specific activator protein. C/EBP CCAAT/enhancer binding protein. PU.1 – Spi1 equivalent in humans, ets transcription factor Induced by IL-4/IL-13 and CD40 ligation Activation of the Ie promoter Activation/cytokine responsive promoter
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Ce1 Ce2 Ce3 Ce4 Se Ie Stat6 NFkB C/EBP PU.1 Germline IgE transcripts Transcription Why has this mechanism evolved to transcribe just the C region? VHDHJH is needed to make a functional IgE Why is the epsilon switch region spliced out? DNA Ce1 Ce2 Ce3 Ce4 Se Ie RNA Ce Ie Spliced RNA Germline transcripts
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What do germline transcripts do? Ce Ie Ce1 Ce2 Ce3 Ce4 Se Ie RNA Spliced RNA Se RNA Ce1 Ce2 Ce3 Ce4 Se Ie Stat6 NFkB C/EBP PU.1 S region RNA hybridises with template DNA
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Single stranded DNA Ie Ce1 Se Se 5’ 3’ Se Se R loop 1. S region in the genomic DNA ‘melts’ 2. S region RNA spliced from germline RNA transcript hybridises to single-stranded DNA 3. ssDNA R loop formed – a substrate for AID - ACTIVATION- INDUCED CYTIDINE DEAMINASE Mechanism of class switch recombination
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NFkB Stat6 Activation-induced cytidine deaminase gene Activation-induced cytidine deaminase Soluble help via Th cell IL-4 or IL-13 Induces Stat 6 Cognate help via Th cell CD40 L from T helper Releases NFkB from IkB B cell activation by antigen leads to: AID gene is expressed under the same conditions as B cells induced to switch Ig isotype
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Expressed only in B cells Involved in isotype class switching & somatic hypermutation AID knockout mice do not class switch Ig isotype Ectopic expression in non B cells causes class switch Mutation in the AID gene can cause hyper IgM syndrome Deaminates cytidine on ssDNA, i.e. substitutes U for C Activation-induced cytidine deaminase
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AID RPA AID RPA AID RPA AID RPA AID RPA AID RPA AID RPA AID RPA GGGCTGGGCTGAGCTGRGCTGAGCTGRGCTGAGCTRARNT CCCGACCCGACTCGACYCGACTCGACYCGACTCGAYTYNA IgE S region Non-template strand is G-Rich and contains RGYW (A/G G T/C A/T) motifs Preferred Se region target sequence for AID GGGCTGGGCTGAGCTGRGCTGAGCTGRGCTGAGCTRARNT AID RPA AID RPA Replication protein A (RPA) targets AID to ssDNA in R loops by binding to RGYW motifs
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GGGCTGGGCTGAGCTGRGCTGAGCTGRGCTGAGCTRARNT GGGCTGGGCTGAGCTGRGCTGAGCTGRGCTGAGCTRARNT CCCGACCCGACTCGACYCGACTCGACYCGACTCGAYTYNA Non-template ssDNA RNA/template DNA hybrid GGGCTGGGCTGAGCTGRGCTGAGCTGRGCTGAGCTRARNT GGGCTGGGCTGAGCTGRGCTGAGCTGRGCTGAGCTRARNT CCCGACCCGACTCGACYCGACTCGACYCGACTCGAYTYNA Activation induced cytidine deaminase NH2 N N O Cytidine O N HN O Uridine AID AID mediated deamination of cytidine to Uridine Activation induced cytidine deaminase AID may also deaminate C on the template strand ?RNAase?
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GGGUTGA CCCGACT GGGUTGA CCCGACT S region DNA now contains mismatched G – U pairs that must be repaired e.g. by the base excision repair mechanism GGGUTGGGUTGAGUTGRGUTGAGUTGRGUTGAGUTRARNT CCCGACCCGACTCGACYCGACTCGACYCGAUTCGAYTYNA G - U mismatch repair GGGUTGGGUTGAGUTGRGUTGAGUTGRGUTGAGUTRARNT CCCGACCCGACTCGACYCGACTCGACYCGAUTCGAYTYNA P P P P P P P P P P P P GGGUTGGGUTGAGUTGRGUTGAGUTGRGUTGAGUTRARNT CCCGACCCGACTCGACYCGACTCGACYCGAUTCGAYTYNA Uracil-DNA glycolase (UNG) removes uracil to leave abasic sites in S region UNG UNG UNG UNG UNG UNG UNG UNG Base is removed, but backbone remains intact
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GGGUTGA CCCGACT P P P P P P P P P P P P G - U mismatch repair APE1 Abasic site is processed by the apurinic/apyrimidimic endonuclease 1 (APE1) GGGUTGA CCCGACT P P P P P P P P P P P P OH DNA is now nicked to produce a single strand break GGGUTGGGUTGAGUTGRGUTGAGUTGRGUTGAGUTRARNT CCCGACCCGACTCGACYCGACTCGACYCGAUTCGAYTYNA APE1 APE1 GGGCTGGGU TGAGCTGRGCTGAGCTGRGCTGAGCTRARNT CCCGACCCGACTCGACYCGACTCGACYCGAU TCGAYTYNA Similar mechanism on the template strand creates a staggered double strand break
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Processing of staggered ends GGGCTGGG CCCGACCCGACTCGACYCGACTCGACYCGA TGAGCTGRGCTGAGCTGRGCTGAGCTRARNT TCGAYTYNA GGGCTGGG TGAGCTGRGCTGAGCTGRGCTGAGCTRARNT CCCGACCCGACTCGACYCGACTCGACYCGA TCGAYTYNA End fill-in reactions ACTCGACYCGACTCGACYCGAC Exonuclease activity Ca2 Ce Cg4 Cg2 Ca1 Cg1 Cg3 Cd Cm Sg3 Sg1 Sa1 Sg2 Sg4 Se Sa2 Sm
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Ca2 Ce Cg4 Cg2 Ca1 Cg1 Cg3 Cd Cm Sg3 Sg1 Sa1 Sg2 Sg4 Se Sa2 Sm Cm Cd Cg3 VDJ Cg1 Ca1 Cg2 Cg4 Ce Ca2 VDJ Ce Ca2 Cm Cd Cg3 Cg1 Ca1 Cg2 Cg4 Excised episomal circle of intervening DNA Activation of Im & Ie promoter by Ag, IL-4/13 and CD40L Production of germline transcripts and splicing of Sm and Se Deamination of ssDNA in Sm and Se by AID Base excision and mismatch repair Blunt-ended ds breaks and synapsis of Sm to Se by non-homologous end joining Process occurs in two S regions simultaneously
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After N and P nucleotides have been inserted, several other proteins, (Ku70:Ku80, XRCC4 and DNA dependent protein kinases,ARTEMIS exonuclease, DNA ligase IV) bind to the hairpins and the heptamer ends. Ig gene recombination 7 23 9 7 12 9 Non-homologous end joining in class switch V D J Closely resembles another B cell Ig gene mechanism Defects in NHEJ proteins impair class switch
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Stat6 NFkB C/EBP PU.1 BSAP BCL-6 BCL-6 BCL-6 BCL-6 binds to the Stat-6 binding site and represses switching Stat6 is involved in Th2 cell differentiation, the expression of CD23 (the low affinity IgE receptor) and VCAM expression BCL-6 may exert it’s anti/pro-allergic activities via these genes Stat6 Transcription blocked BCL-6 -/- mice have enhanced IgE isotype switching BCL-6 -/- Stat6 -/- mice have no IgE An RFLP has been mapped to the first intron of the BCL-6 gene that is significantly associated with atopy - but not IgE levels
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Additional areas to think about Can’t get over a 2.2 mark without showing evidence of outside reading in answers
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Relationship between isotype switch, somatic hypermutation and proliferation of B cells in the germinal centre What is the relationship between the deliberately mutagenic mechanisms of isotype switch and somatic hypermutation in B cells and the propensity of B cells to form tumours Where are the holes in the ‘skew to Th2’ model of allergy? What are allergic responses really for?
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What are allergic immune responses really for? Trichuris Trypanosoma Toxoplasma Enterobious Ascaris Leishmania Schistosome Hookworm Plasmodium Wuchereria Onchocerca Taenia
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Text book view Helminth infections induce IgE, mastocytosis and eosinophilia A classic Th2-driven response Eosinophils killing a schistosome egg in vitro
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Susceptible mice However…….. Heavily parasitised individuals exist - despite Th2 responses and eosinophilia. Scarce in vivo evidence of eosinophil and IgE control of helminth infection Yet IL-4 may be involved - Trichuris muris model Resistant mice Else et al., 1994 J. Exp Med 179 347-351
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Nippostrongylus infection Th2 cells themselves may not be needed IL-4 from any source is sufficient to induce worm expulsion IL-4 Urban et al., 1995 J. Immunol. 154, 4675-4684