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  • 1
    Online Resource
    Online Resource
    Basel :S. Karger AG,
    Keywords: Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (243 pages)
    Edition: 1st ed.
    ISBN: 9783805586290
    Series Statement: Chemical Immunology and Allergy Series ; v.94
    DDC: 616.97
    Language: English
    Note: Cover -- Contents -- Preface: Role of T-Cell Subtypes in Allergic Inflammations -- Th17 and Treg Cells Innovate the Th1/Th2 Concept and Allergy Research -- Abstract -- General Role of T Cells in the Immune System -- Treg Cells and Their Importance in Allergy -- Th17 Cells - Proinflammatory Cousins of Treg Cells? -- Origin of T-Cell Phenotypes -- Future and Perspective -- Acknowledgements -- References -- Regulatory T Cells and Antigen-Specific Tolerance -- Abstract -- Characteristics of Regulatory T Cells -- Intra- and Extrathymic Generation of Tregs -- Function of Tregs -- Concluding Remarks -- References -- Molecular Mechanisms of Regulatory T-Cell Development -- Abstract -- Role of Foxp3 in TR Cell Function -- Molecular Mechanisms of nTR Cell Development in the Thymus -- Function of Foxp3 in nTR Cell Development -- Transcriptional Regulation by Foxp3 -- The Foxp3 Transcriptional Program and the TR Cell Transcriptosome -- Transcriptional Regulation of Foxp3 -- nTR versus iTR Cells -- Heritable Disorders of TR Cells -- TR Cell-Directed Therapeutic Interventions in Allergy and Autoimmunity -- Concluding Remarks -- References -- Interaction of Regulatory T Cells with Antigen-Presenting Cells in Health and Disease -- Abstract -- Dendritic Cells and Regulatory T Cells -- Maturation Status of Dendritic Cells Is Critical for Induction of Regulatory T Cells -- Regulatory T Cells Suppress DC Maturation -- Monocytes/Macrophages and Regulatory T Cells -- B Cells and Regulatory T Cells -- Interaction between DCs and Regulatory T Cells during Allergic and Inflammatory Reactions -- Conclusion -- References -- Mucosal Regulatory T Cells in Airway Hyperresponsiveness -- Abstract -- Respiratory Tolerance -- Asthma -- Measuring AHR -- AHR in Asthma -- Studying AHR in Animal Models -- Inhibiting AHR in Animal Models -- Treg Populations. , Role of Treg in Inhibiting AHR -- Role of Treg in Human AHR -- Therapeutic Means of Inhibiting AHR in Asthma -- Conclusions -- References -- Natural Killer Cells in Allergic Inflammation -- Abstract -- Human Natural Killer Cell Subtypes -- Lysis by NK Cells -- NK Cells and Cytokines -- NK Cells in Allergy -- Concluding Remarks -- References -- Mast Cells and Mast Cell-Derived Factors in the Regulation of Allergic Sensitization -- Abstract -- Skin Models Implicate a Role for Mast Cells in Priming of Adaptive Immune Responses and Allergic Sensitization -- Mast Cells Initiate and Modulate T-Cell Responses during Allergic Airway Inflammation -- Novel and Distinct Roles for Basophils in Allergy -- Conclusion -- Acknowledgements -- References -- Regulatory Effects of Histamine and Histamine Receptor Expression in Human Allergic Immune Responses -- Abstract -- Molecular Basis for Action -- Histamine Receptors -- Synthesis and Metabolism of Histamine -- Histamine in Chronic Inflammatory Responses -- Role of Histamine in the Regulation of Immune Response -- Antigen-Presenting Cells -- Effect of Histamine on T Cells and Antibody Isotypes -- Role of Histamine and H1 Antihistamines during Allergen-SIT -- Use of H1 Antihistamines in Asthma -- Conclusions -- Acknowledgments -- References -- T-Cell Regulation in Asthmatic Diseases -- Abstract -- New Molecular Target for Allergic Asthma -- Interleukin-6 as a Bridge between Innate and Adaptive Immune Responses -- Interaction of Th2 and T-Regulatory Cells -- Do Th17 Cells Counteract T-Regulatory Cells in Allergic Asthma? -- T-Bet Deficiency: Genetic and Epigenetic Control in Allergic Asthma -- Glucocorticoid Receptor and T-Cell-Specific Transcription Factors -- Conclusions -- Acknowledgment -- References -- Immune Regulatory Mechanisms in Allergic Contact Dermatitis and Contact Sensitization -- Abstract. , Contact Hypersensitivity and Animal Model of Tolerance to Haptens -- T-Regulatory Cells in Contact Allergy -- Dendritic Cells as Orchestrators of Skin Immune Responses to Haptens -- Conclusions -- References -- Regulatory Role of T Lymphocytes in Atopic Dermatitis -- Abstract -- Regulation of Atopic Dermatitis by T Cells - Clinical Aspects -- T Lymphocytes Dominate the Cellular Infiltrate in Atopic Dermatitis -- Role of Adaptive Immune Responses in Atopic Dermatitis Involving IgE Responses -- Aeroallergen-Specific T Cells Are Well-Known Initiators and Perpetuators of Eczematous Responses in Atopic Dermatitis -- Food-Specific T Cells Are Involved in Allergic Responses in Atopic Dermatitis in Children and Adults -- T Cells May Contribute to the Defects in Innate Immune Response in Atopic Dermatitis -- Microorganism Activate T Lymphocytes and Bystander Cells in the Skin in Atopic Dermatitis -- Are T Cells Involved in Specific Immune Responses to Autoantigens in Atopic Dermatitis? -- Cellular and Molecular Interactions of T Cells in Atopic Dermatitis -- T Cells Communicate with Vascular Cells, Proinflammatory Cytokines and Chemokines in the Skin -- Do CD8+ T Cells Play a Role in Atopic Dermatitis? -- T Cells Secrete Different Cytokines at Different Stages in Atopic Dermatitis -- T Lymphocytes Regulate the Cutaneous Cytokine Milieu in Atopic Dermatitis -- Th-2 Cytokines Have Numerous Effects on Cutaneous Cells in Atopic Dermatitis -- Do Th-17 Lymphocytes Contribute to Eczema in Atopic Dermatitis? -- Role of Regulatory T Cells in Atopic Dermatitis -- T Cells Interact with Keratinocytes in Atopic Dermatitis -- Concluding Remarks -- References -- T-Cell Regulation in Helminth Parasite Infections: Implications for Inflammatory Diseases -- Abstract -- Epidemiology of Helminth Infections, Allergies and Autoimmune Pathologies. , Immune Regulation in Human Helminth Infections -- Experimental Evidence for Immune Regulation in Animal Models -- Models of Allergies and Autoimmunity - Helminths Acting Through T Cells? -- Helminths and the Innate Immune System -- Learning from Helminths to Treat Allergy and Autoimmunity -- Acknowledgements -- References -- Immune Regulation and Tolerance to Fungi in the Lungs and Skin -- Abstract -- Fungal Diseases -- Features of Fungal Diseases -- Immunity to Fungi: Connecting the Innate to the Adaptive Immune System through DCs -- Innate Immunity -- Dendritic Cells -- Adaptive Th Immunity -- Driving Inflammation: Contribution of the Th17 Pathway -- Dampening Inflammation and Allergy to Fungi: The Role of Treg Subsets -- Tryptophan Catabolism and Allergy: Fungi Are Next in Line -- Paradigm of Reverse and Noncanonical in Fungal Infections -- R& -- N in Fungal Infections Is Not Toll-Free and Is Exploited by Corticosteroids -- Can IDO Help in the Fight Against Fungal Allergy? -- Conclusion: Targeting R& -- N-Mediated Immune Homeostasis in Fungal Allergy -- Acknowledgements -- References -- Control of Delayed-Type Hypersensitivity by Ocular-Induced CD8+ Regulatory T Cells -- Abstract -- Suppression of Cell-Mediated Immunity by CD8+ Regulatory T Cells -- Suppressor T Cells Redux -- Suppression of the DTH Response -- Induction of Splenic CD8+ Suppressor T Cells via the Eye's Anterior Chamber -- Afferent and Efferent Mechanisms for Ocular-Induced CD8+ Regulatory T Cells -- Antigen Specificity of the Suppression of DTH by CD8+ Regulatory T Cells -- Qa-1b Restriction of CD8+ Suppressor T-Cell-Mediated Suppression -- IFN-gamma Facilitates the Suppression of DTH by Splenic CD8+ Suppressor T Cells -- TGF-beta Is a Mechanism of CD8+ Treg-Mediated Suppression of DTH -- Conclusion -- Acknowledgements -- References. , Novel Therapeutic Strategies by Regulatory T Cells in Allergy -- Abstract -- Role of T-Regulatory Cells in Inhibiting Allergic Diseases -- Implications from Mouse Models -- Evidence for Targeting Treg Cells -- Therapeutic Strategies for Modulating Treg Activity in Allergy -- Induction of Treg Activity by Peptide-Based Immunotheraphy -- Induction of Treg Activity by Targeting Toll-Like Receptors -- Conclusion -- References -- T-Cell Regulatory Mechanisms in Specific Immunotherapy -- Abstract -- Peripheral T-Cell Tolerance in Allergen-Specific Immunotherapy -- Peripheral T-Cell Tolerance to Allergens Is Associated with Regulation of Antibody Isotypes and Suppression of Effector Cells -- T-Regulatory Cells -- Tr1 Cells -- Th3 Cells -- CD4+CD25+ Treg Cells -- Other T-Regulatory Cells -- B-Regulatory Cells -- Dendritic-Regulating Cells -- Other Cells with a Possible Regulatory Function -- Suppression Mechanisms of T-Regulatory Cells -- Clinical Relevance of T-Regulatory Cells -- cAMP-Stimulating G-Protein-Coupled Receptors in Peripheral Tolerance -- Clinical Evidence for T-Regulatory Function of Histamine Receptors -- Conclusion -- References -- Control and Regulation of Peripheral Tolerance in Allergic Inflammatory Disease: Therapeutic Consequences -- Abstract -- Pathobiology of the Allergic Inflammatory Response -- Regulation of Peripheral T-Cell Tolerance and Aberrations in Allergic Diseases -- T-Cell Anergy -- Suppressive Cytokines (IL-10, TGF-beta) -- Natural and Adaptive Treg Cells -- Mechanisms Promoting the Inflammatory Response in Allergic Diseases -- Tumor Necrosis Factor-alpha -- Thymic Stromal Lymphopoietin -- Interleukin-25 -- Natural Killer T Cells -- Immunotherapeutic Approaches for Regulation of T-Cell Tolerance in Allergic Diseases -- Conclusions and Future Directions -- References. , Lung Dendritic Cells: Targets for Therapy in Allergic Disease.
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Scandinavian journal of immunology 27 (1988), S. 0 
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: In earlier work we have observed strain- and age-related diversity of immunological ageing in inbred mice pretreated with tolerogen or left without pretreatment and then immunized. Different isotype show different age- and strain-related changes. Here, we extend this isotype analysis from C57BL/6 and SJL to A/J. By comparison with the first two of these, animals of strain A/J show very little age-related change, as judged by indirect plaque-forming response. We have found that in A/J, as in SJL and CS7BL/6 mice, age-related changes are isotype-dependent. The age-related changes in isotype predominance and magnitude differ for different determinants. They depend on the structural relation between the tolerance-inducing or -sensitizing macromolecule and the immunogen.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK; Malden, USA : Blackwell Science Ltd
    Scandinavian journal of immunology 61 (2005), S. 0 
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Difficult-to-treat asthma (DTA) represents a heterogeneous subgroup of asthma. Up to now, the lack of specific diagnosis not only complicates appropriate specification and control of asthma, but also makes targeted research difficult. The aim of this study is to categorize this heterogeneous group of DTA patients (n = 27; referring to the GINA guidelines) based on the distinct leucocyte redistribution (LR) after glucocorticoid (GC) treatment. Furthermore, the effect of adjuvant therapies was investigated for its impact on LR. The frequency of CD3+, CD4+, CD8+, CD14+, CD19+ and NK cells was analysed in peripheral blood before and 3 h after systemic GC treatment, along with the markers of activation HLA-DR and CD25. Within 3 h of GC administration, a significant average decrease of 16% in CD3+CD4+ (P ≤ 0.001) and a 12% increase in NK-cell frequency (P ≤ 0.001) clearly distinguished two groups of patients: LR-responsive and LR-unresponsive patients. The CD3+CD8+ T-cell number and activation marker remained unchanged. Patients who received adjuvant therapy, such as methotrexate or interferon-α, because of poor clinical response to GC showed an LR similar to that showed by responsive patients. DTA patients comprise at least two immunologically distinct groups: patients showing an immediate decrease in CD3+CD4+ T cells and an increase in NK cells following GC administration and patients lacking an immediate change. Analysis of LR not only may allow the identification of immunologic steroid resistance, but also may be of value for immunologic determination of effective steroid doses.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK; Malden, USA : Blackwell Science Ltd/Inc.
    Scandinavian journal of immunology 59 (2004), S. 0 
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: The endogenous nucleoside adenosine is released in excess during inflammation or other metabolic stress and is generally known to deliver tissue protective anti-inflammatory effects. Adenosine acts via four adenosine receptors of which the A2a receptor is the predominant form in T cells. Adenosine levels are elevated in asthmatic lung, and adenosine can directly induce mast cell degranulation and bronchoconstriction in these patients. Instead, the role of anti-inflammatory mechanisms of adenosine on T cells in asthma is unclear.Aim:  To study the A2a receptor expression in peripheral blood CD4+ T cells in asthmatic and healthy individuals using flow cytometric and quantitative real-time PCR methods.Results:  Unstimulated CD4+ cells of asthmatic patients expressed significantly lower levels (P 〈 0.001) of A2a receptor in protein level (mean percentage of cells positive ± SEM: 76.8 ± 1.2, n = 6) compared to healthy individuals (90.4% ± 1.9, n = 4). Double staining for CD69 expression showed that stimulation of CD4+ cells decreased A2a expression in both groups but indicated that the detected lower levels of A2a in unstimulated cells of asthmatics was not due to preactivation in these patients. Surprisingly, A2a mRNA expression in unstimulated CD4+ cells was significantly higher (P 〈 0.05) in asthmatics (n = 28) compared to healthy controls (n = 7). The expression did not correlate with serum total IgE levels.Conclusions:  Asthmatic individuals express less A2a adenosine receptor on their peripheral CD4+ T cells. The higher mRNA levels instead may point to a negative feedback regulation in the receptor expression. The role of possibly decreased adenosine-mediated anti-inflammatory effects in asthma pathogenesis require further studies on this T-cell mediated disease.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1365-2222
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background We report the results of a study comparing the recombinant Aspergiilus fumigatus allergen I (rAsp f I) to commercial A. jumigatus extracts in serological assays, Pharmacia CAP System and skin tests.Objective The study was designed to test the feasibility of using recombinant allergens in an automated serology system for determination of allergen-specific IgE.Methods Patients with allergic bronchopulmonary aspergillosis (ABPA), asthmatics with A. fumigatus allergy and control subjects, who included allergic asthmatics without allergy to A. fumigatus and healthy subjects, were investigated. All subjects were characterized with respect to their total IgE level, radio allergosorbent test to A. fumigatus and skin test reactivity to both commercial A. fumigatus extracts and recombinant rAsp f I protein.Results All patients with ABPA (n = 30) showed positive skin test reactions with commercial A. fumigatus extracts, and 24 were sensitized to r Asp f I by the same criterion. The 10 patients with asthma and A. fumigatus allergy showed positive skin reactions to at least one commercial extract, and five reacted to r Asp f I. AU control subjects (H= 19) scored negatively in skin tests to A. fumigatus extracts and r Asp f I, and showed no detectable rAsp f I-specific IgE. ImmunoCAP carrying immobilized r Asp f I were evaluated using sera from all individuals described and the results compared with those obtained with the r Asp f I-specific ELISA for IgE. The data obtained with the two r Asp f I-specific detection systems correlated closely (r= 0.997) and were in perfect agreement with the skin test results.Conclusion The data show that r Asp f I can be used as immobilized allergen in the Pharmacia CAP System indicating the feasibility of using recombinant allergens for an automated serological diagnosis of allergic diseases. However, every recombinant allergen needs to be evaluated individually for its performance if applied to a new diagnostic technology.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1365-2222
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: In the first part of this study peripheral blood lymphocyte subpopulations. Iheir activation slate and various serum parameters were measured in extrinsic and intrinsic atopic dermatitis (AD) patients compared to normal individuals. Beside the characteristic eosinophilia, significantly increased numbers of CD4+ T cells with increased expression of IL-2 receptors (IL-2R) and HLA-DR were noted in the AD patients. In addition, extrinsic AD patients showed increased numbers of CD23+ B cells and decreased numbers of CD16+ natural killer cells. Moreover, increased serum levels of eosinophil canonic protein (ECP) and soluble 1L-2R as well as soluble factors lhat prolong survival of eosinophils in vitro could be demonstrated. In the second section of this study we determine how these blood immunological parameters relate to the clinical severity of the skin lesions of AD, by weekly analysis of 12 AD patients attending a high altitude clinic for 3 to 6 weeks. The patients were divided into two groups on the basis of treatment with topical steroids, but during the observation period a significant improvement in clinical status was observed in all AD patients independent of topical steroid therapy. A progressive decrease in eosinophil and activated T cell numbers. soluble IL-2R levels and serum eosinophil survival prolonging activity could be demonstrated, which closely correlated with the clinical severity of the AD.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1365-2222
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background Diagnostic procedures using natural extracts show only limited quantitative correlation between in vivo and in vitro results. Highly pure recombinant allergens might show more predictive findings.Objective The aim of this study was to compare natural birch pollen extract (BPE) and recombinant Betula verrucosa (rBet v 1) for their diagnostic value comparing skin prick tests (SPTS) and nasal provocation tests (NPTS) with specific IgE in the serum.Methods Thirty-four patients allergic to birch pollen and five healthy controls were investigated. SPT and NPT were performed with BPE and rBet v 1 at different concentrations. Specific serum IgE was measured by the Pharmacia CAP system.〈section xml:id="abs1-2"〉〈title type="main"〉Results Commercial BPE and rBet v 1 (10 μg/mL) were able to elicit similar allergenic reactions in vivo and IgE binding in vitro. SPT reflects immediate-type allergy as determined by NPT to a higher degree than specific IgE, for both reagents. To cause allergic reactions in NPT, higher amounts of rBet v 1 were needed than for skin tests and the sensitivity was lower than with BPE.〈section xml:id="abs1-3"〉〈title type="main"〉Conclusion rBet v 1 alone is sufficient for a reliable diagnosis of birch pollen allergy in most patients and induces comparable skin test reactivity as BPE, but less allergic reactions in nasal provocations.
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  • 8
    ISSN: 1365-2222
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background For many years, fungal spores have been recognized as potential causes of respiratory allergies. All fungal allergens cloned so far represent either secreted or cytoplasmatic proteins, but nothing is known about the involvement of fungal surface proteins in allergic diseases.Methods A phage surface displayed cDNA-library from the mould Cladosporium herbarum was constructed and phage displaying IgE-binding proteins were selectively enriched with immobilized serum IgE from C. herbarum-sensitized individuals. Inserts encoding putative allergens were sequenced, subcloned and used to produce recombinant proteins. Allergenicity of the proteins was evaluated by IgE binding in Western blots, enzyme-linked immunosorbent assay (ELISA) and skin prick test in a total of 84 patients sensitized to either C. herbarum or Aspergillus fumigatus and three healthy controls.Results After four rounds of affinity selection, the cDNA-library was enriched for clones displaying IgE-binding molecules. Sequencing of inserts showed that one clone contained an open reading frame predicting a protein of 105 amino acids and a calculated molecular weight of 10.5 kDa showing the classical signature of members of the hydrophobin family. The recombinant protein, termed HCh-1, was able to bind IgE from six patients sensitized to fungi in vitro. Two of those patients were also included in a skin prick test survey and showed strong type I skin reactions to HCh-1, demonstrating the allergenic nature of C. herbarum hydrophobin and indicating a prevalence of sensitization in the range of 8–9%. In contrast, the hydrophobin HYP1 from Aspergillus fumigatus was not recognized by the sera of the same patients and controls investigated with HCh-1.Conclusion C. herbarum hydrophobin represents the first component of the cell wall of fungi demonstrated to act as a rare but clinically relevant allergen in vitro and in vivo.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Clinical & experimental allergy 27 (1997), S. 0 
    ISSN: 1365-2222
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background In diagnosis of type I allergy recombinant allergens have potential advantages over conventional allergenic extracts, both regarding specificity and reproducibility.Objectives We therefore decided to study honey bee venom (BV) and its major allergen phospholipase A2 (PLA) in native and recombinant form for diagnosis of bee sting allergy.Method We investigated 85 patients with a history of a recent systemic allergic bee sting reaction and positive intracutaneous skin test to BV, and 21 controls with no history of allergic bee sting reaction and negative skin test to BV. Intracutaneous skin tests and determination of specific IgE by ImmunoCAPR to BV, native PLA (nPLA) and recomhinant PLA (rPLA) were done in all patients and controls.Results In skin testing 84 (99%) of the 85 patients reacted to nPLA and 81 (95%) to rPLA, while none of the 21 controls was positive with nPLA or rPLA. Specific serum IgE to BV could be detected in 82 of the patients (96%), to nPLA in 73 (86%) and to rPLA in 66 (78%). Four (19%) of the controls had a positive CAP to BV, one (4.8%) to nPLA and none to rPLA. Analysis of discordant results in CAP showed, that most patients with specific IgE to BV, but not to nPLA and rPLA, had positive skin tests to both PLA preparations and low levels of BV specific IgE. Patients with specific IgE to nPLA but not to rPLA were usually sensitized to minor allergens of BV which contaminated the commercial nPLA.Conclusions PLA is the major allergen in BV. While diagnostic tests with BV are more sensitive, the specificity of tests with PLA, especially rPLA is clearly increased as compared with BV.
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Ltd
    Clinical & experimental allergy 34 (2004), S. 0 
    ISSN: 1365-2222
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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