L’allergie est une pathologie touchant un très grand nombre de personnes à travers le monde en particulier dans les pays industrialisés. Actuellement seule l’éviction totale de l’allergène évite toute nouvelle réaction allergique. Jusqu’à présent différents types de tests ont été développés afin de déterminer le pouvoir allergisant d’un grand nombre de composés. Parmi ces tests certains font appel à l’utilisation de la voie animale. Cependant, dans le cadre de la législation sur les cosmétiques ces tests sont amenés à disparaître. Dans ce contexte il est nécessaire de développer des stratégies intégrées combinant à la fois des tests in silico, in chemico et in vitro. Ce travail de thèse propose d’analyser des données de réactivité issues de tests « in chemico » réalisés au laboratoire, et de les comparer avec des données biologiques issues de tests « in vitro » sur l’activation de la voie Keap1/Nrf2/ARE chez les lignées de cellules dendritiques de type THP-1 et MoDCs (INSERM UMR-996). Ainsi, la réactivité de 10 composés connus pour leur implication dans des réactions allergiques a été étudiée au cours de ce travail permettant d’apporter des éléments de réponse sur l’existence d’une corrélation entre la capacité d’une molécule à réagir avec une protéine, et donc à être sensibilisante, et le stress oxydant induisant la maturation des cellules dendritiques. / Contact dermatitis is one of the most common health problems and is highly prevalent in industrialized countries. Currently, only the total eviction of the allergen can prevent further allergic reactions. Since several years, different tests have been developed to determine the sensitization potential of a large number of compounds. Some of them are based on animal models. However, the cosmetic legislation now bans this kind of tests. In this context, the development of integrated strategies based on in silico, in chemico and on in vitro assays seems to be necessary. The aim of this PhD work is to compare reactivity data from in chemico tests realized at the laboratory, with biological data obtained from in vitro tests concerning the activation of the Keap1/Nrf2/ARE pathway in THP-1 and MoDCs dendritic cells (INSERM UMR-996). The reactivity of 10 compounds known for their implication in allergic contact dermatitis has been studied to show if a correlation exists between the potential of sensitization of allergens and the oxidative stress inducing dendritic cells maturation.

Charles University Faculty of Pharmacy in Hradec Králové Department of Biological and Medical Sciences Author: Bc. Petra Porubová Supervisor: prof. RNDr. Ctirad Andrýs, Ph.D. Title of diploma thesis: Allergic phenotypes in patients with respiratory allergy evaluated by microchip ISAC technique Key words: allergic inflammation, allergen specific IgE, component resolved diagnostics, microchip, ISAC Background: The aim of this diploma thesis was to evaluate the sensitization profile in the group of pacients with allergic rhinitis and/or bronhial asthma and to identify possible differences between patients with different disease severity. Methods: ImmunoCAP ISAC was used to determine specific IgE antibodies against 112 allergen components. The evaluated group included 152 patients (57.9 % women) from the allergology outpatient office of the Department of Clinical Immunology and Allergology, University Hospital Hradec Králové. Results: The most common allergens in this group of patients were the components Phl p 1 (68,4 %) and Bet v 1 (65,1 %). Differences in the number of positive and negative reactions were demonstrated between patients with different severity of allergic rhinitis. Correlations were found between the number of positive/negative reactions and the severity of bronchial asthma. And the...

There is concern about the indoor environment in aircraft but few stud-ies exist on self-rated health (SRH) and respiratory symptoms among pilots. Occupational and non-occupational risk factors for SRH, respira-tory symptoms and other symptoms among commercial pilots were investigated in this thesis. One cohort study and one prevalence study were performed among pilots in one Scandinavian airline company. Fungal DNA, furry pet allergens and volatile organic compounds of microbial origin (MVOC) were measured on board. Cat (fel d1), dog (Can f1) and horse (Ecu cx) allergens were found in all dust samples and allergen levels were 27-75 times higher in aircraft with textile seats as compared to leather surfaces. The sum of MVOCs in the cabin air was 3.7 times higher than in homes in Uppsala and 2-methyl-1-butanol and 3-methyl-1-butanol concentrations were 15-17 times higher. Asper-gillus/Penicillium DNA and Aspergillus versicolor DNA were more common in aircraft with textile seats. One fifth reported SRH as poor or fair, 62% had fatigue, 46% overweight/obesity and 71% insomnia. Poor or fair SRH was associated with overweight/obesity, lack of exercise, insomnia, low sense of coherence (SOC) and high work demand. Re-covery from work was worse among those with insomnia and low social support at work. Fatigue was more common among young or female pilots and related to insomnia and high work demand. Pilots flying MD80 or Saab 2000 aircraft had less fatigue. Pilots exposed to environmental tobacco (ETS) on board had more eye symptoms and fatigue which were reduced after the ban of smoking (in 1997). Pilots with increased work demand developed more rhinitis, dermal symptoms and fartigue and those with decreased work control developed more eye symptoms. The incidence of doctors’ diagnosed asthma and atopy were 2.4 and 16.6 per 1000 person years, respectively. Pilots changing type of flight got more airway infections. Those reporting decreased work control had a higher incidence of atopy. Risk factors in the home environment included ETS, dampness or mould, window pane condensation in winter and living in houses built after 1975. In conclusion, SRH and respiratory health among pilots are associated with specific occupational and non-occupational risk factors.

This diploma thesis was focused on the study of lysozyme and lysozyme-like proteins, either of similar function (antibacterial) or molecular weight (14 - 17 kDa), of synanthropic acaroid mites. In general, animals utilize lysozymes for defensive (antimicrobial) or digestive purposes but also as a digestive enzyme. Some chitinases or other enzymes that act similarly to lysozyme can be utilized for similar purposes. Chitinases belong to house dust mite allergens. One of major mite are historically named lysozyme-like proteins which name relates to their size similar to lysozyme. Bacteriolytic activity has also 14.5 kDa (UniprotKB Q8MWR6) protein. The species selected for the study were domestic mites Dermatophagoides farinae, D. pteronyssinus and Lepidoglyphus destructor. Presence of lysozyme was detected by direct detection with polyclonal antibody using immunohistochemistry and dot blots. Immunohistochemistry proved presence of lysozyme epitopes in the feces of D. farinae, D pteronyssinus a L. destructor. Dot blot analysis demonstrated the presence of imunoreactivity of antibody in spent growth medium extracts (SGME) of all three species. This implies that lysozyme is synthesized in the midgut. The presence of lysozyme and lysozyme-like proteins was proved using 2D electrophoresis and MALDI TOF/TOF...

<p>Immunoglobulin E (IgE)-mediated allergy occurs when our immune system causes a reaction to otherwise harmless substances (allergens). Allergens are predominantly proteins present in biological materials such as pollens, mites, animal epithelia, moulds and foods. </p><p><i>In vitro</i> tests for specific IgE antibodies usually employ an allergen source extract as an antibody capturing reagent. The proportion of allergenic molecules in these biochemically complex extracts may vary.</p><p>Recombinant allergens may be obtained in large quantities with biotechnological techniques. These proteins can be characterized biochemically and immunologically, resulting in tests with minimal batch-to-batch variation. This thesis describes different uses of recombinant allergens in component-resolved diagnostics (CRD).</p><p>In CRD, single allergenic proteins are used to establish a sensitization profile of the patient. Two timothy grass (<i>Phleum pratense</i>) pollen allergens, Phl p 11 and Phl p 4, were cloned and expressed as recombinant proteins. They were subsequently characterized and can, for example, be used in a panel for grass pollen CRD.</p><p>Single allergens may be useful as diagnostic markers for allergic sensitization. This phenomenon was studied using tropomyosin, a major allergen from the shrimp <i>Penaeus aztecus</i> (Pen a 1). The characteristics of the recombinant and natural proteins were compared. The recombinant tropomyosin was then extensively tested using specific competition for IgE binding against extracts of other crustacean species, house dust mite and cockroach.</p><p>In cases when an important allergen is missing or underrepresented in a natural extract, the corresponding recombinant allergen may be added to the extract as a spiking reagent. Previous studies have shown that latex extracts for diagnostic testing may lack the allergen Hev b 5. Recombinant Hev b 5 was expressed from a synthetic gene construct, incorporating several adaptations to enable efficient large scale production of the recombinant protein, to be used as a spiking reagent.</p>

Immunoglobulin E (IgE)-mediated allergy occurs when our immune system causes a reaction to otherwise harmless substances (allergens). Allergens are predominantly proteins present in biological materials such as pollens, mites, animal epithelia, moulds and foods. In vitro tests for specific IgE antibodies usually employ an allergen source extract as an antibody capturing reagent. The proportion of allergenic molecules in these biochemically complex extracts may vary. Recombinant allergens may be obtained in large quantities with biotechnological techniques. These proteins can be characterized biochemically and immunologically, resulting in tests with minimal batch-to-batch variation. This thesis describes different uses of recombinant allergens in component-resolved diagnostics (CRD). In CRD, single allergenic proteins are used to establish a sensitization profile of the patient. Two timothy grass (Phleum pratense) pollen allergens, Phl p 11 and Phl p 4, were cloned and expressed as recombinant proteins. They were subsequently characterized and can, for example, be used in a panel for grass pollen CRD. Single allergens may be useful as diagnostic markers for allergic sensitization. This phenomenon was studied using tropomyosin, a major allergen from the shrimp Penaeus aztecus (Pen a 1). The characteristics of the recombinant and natural proteins were compared. The recombinant tropomyosin was then extensively tested using specific competition for IgE binding against extracts of other crustacean species, house dust mite and cockroach. In cases when an important allergen is missing or underrepresented in a natural extract, the corresponding recombinant allergen may be added to the extract as a spiking reagent. Previous studies have shown that latex extracts for diagnostic testing may lack the allergen Hev b 5. Recombinant Hev b 5 was expressed from a synthetic gene construct, incorporating several adaptations to enable efficient large scale production of the recombinant protein, to be used as a spiking reagent.

In der heutigen Zeit sind ca. 4000 Verbindungen bekannt, denen die Fähigkeit nachgesagt wird, eine Kontaktallergie auslösen zu können. Die Entscheidung, ob ein Stoff hautsensibilisierende Eigenschaften besitzt, wird dabei meist auf der Grundlage von Beobachtungen am Menschen und/oder von tierexperimentellen Befunden getroffen. Bedingt durch den vermehrten Einsatz exotischer Pflanzen und neu entwickelter synthetischer Substanzen im Bereich der Kosmetikindustrie besteht der Bedarf an einer einfachen Methode zur Vorhersage des kontaktallergenen Potentials einer Verbindung. Als zentraler Schritt bei der Manifestierung einer Kontaktallergie wird die Bildung eines Hapten-Carrier-Komplexes aus dem niedermolekularen Kontaktallergen (Hapten) und Hautproteinen (Carrier) angesehen. Zur Abschätzung der Sensibilisierungsfähigkeit kann daher auch die Reaktivität der Substanz oder ihrer Metaboliten gegenüber Proteinen herangezogen werden. Im Rahmen dieser Arbeit werden neben dem bedeutenden Phytoekzematogen Tulipalin A die bisher wenig untersuchten kontaktallergenen Duftstoffe Geraniol, 7-Hydroxycitronellal, Benzaldehyd, Salicylaldehyd, Vanillin, Zimtaldehyd, a-Amyl-zimtaldehyd und Benzylcinnamat hinsichtlich ihrer Reaktivität gegenüber peptidgebundenen Aminosäuren untersucht. Verwendet werden für diese Modellversuche Hippuryl-Derivate und Acetyl-Derivate der Aminosäuren Lysin, Histidin, Arginin bzw. Cystein sowie zusätzlich Glutathion. Die dabei gewählten Bedingungen sollen eine Adaption an physiologische Gegebenheiten erlauben. Ziel ist es, zu klären, ob die mit diesen Modellversuchen zu gewinnenden Ergebnisse mit dem bekannten kontaktallergenen Potential der eingesetzten Haptene korrelieren und somit geeignet sind, die Sensibilisierungsfähigkeit einer Substanz vorherzusagen. Über Konjugationsprodukte von Kontaktallergenen mit Peptiden oder Proteinen ist in der Literatur sehr wenig bekannt. Daher ist es ein weiteres Ziel dieser Arbeit, individuelle Produkte der Reaktionen der kontaktallergenen Substanzen mit den nukleophilen Aminosäureseitenketten zu isolieren und zu charakterisieren, um so definierte Hapten-Carrier-Konjugate, die unter physiologisch relevanten Bedingungen entstehen können, zu beschreiben. Aufbauend auf den gefundenen Strukturen sollte es auch möglich sein, Hinweise auf eventuelle Reaktionsmechanismen zu erhalten.

Background: According to recent studies in children, IgE sensitization not only against perennial allergens, but also against food allergens, is related to asthma risk and increased airway inflammation. During the last decade, a new technique for IgE determination based on allergen components has become available, but its use in epidemiological studies has been limited. Aims: To investigate the relationship between the pattern of IgE sensitization to allergen components and the prevalence of asthma, airway inflammation and hyperresponsiveness in a population-based setting. To examine the relationship of IgE sensitization to allergen extract, and airway inflammation, airway hyperresponsiveness and blood eosinophilia in asthmatics. To examine the natural history of IgE sensitization to food allergens in adults. To compare extract-based and component-based IgE measurements in relation with new-onset respiratory disease and airway inflammation and hyperresponsiveness. Methods: The present thesis is based on cross-sectional and longitudinal analyses of the adult, the population-based study ECRHS (European Community Health Survey) and a cross-sectional, observational study of young subjects with asthma. IgE sensitization was examined by means of both extract-based and component-based tests. Airway inflammation was assessed by exhaled NO and airway hyperresponsiveness with methacholine test. Results: IgE sensitization to food allergens independently related to increased airway inflammation in both a population-based study and a study of asthmatics. Furthermore, a relation was found with increased blood eosinophils in asthmatics. The decrease in prevalence of IgE sensitization against food allergens during a 9-year follow-up was larger than the decrease of aeroallergens. Subjects with IgE sensitization to both cat extract and components showed more frequent airway inflammation, greater bronchial responsiveness and higher likelihood of developing asthma and rhinitis than subjects with IgE sensitization only to cat extract. Conclusions: The presence of IgE antibodies against food allergens was independently associated with airway and systemic inflammation. Both aeroallergens and food allergens should be examined in order to understand the signaling of local and systemic inflammation in asthma. Prevalence of IgE sensitization to food decreased in adults to a larger extent than IgE sensitization against aeroallergens. Measurement of IgE sensitization to cat allergen components appears to have a higher clinical value than extract-based measurement

L’allergie de contact est une pathologie touchant de 15 à 20 % de la population occidentale. A l’heure actuelle il n’existe aucun traitement, la seule façon efficace de prévention étant l’éviction totale des allergènes. Les tests de sensibilisation de nouvelles molécules avant leur mise sur le marché ont été réalisés sur l’animal jusqu’à l’interdiction dans le 7ème amendement à la directive Européenne concernant l’industrie cosmétique. Dans ce contexte il est primordial de développer des méthodes alternatives. Ce travail de thèse propose d’analyser la problématique de l’allergie de contact en allant de la molécule au tissu pour les allergènes réagissant par voie radicalaire :In chemico : étude de la réactivité des hydroperoxydes allyliques vis-à-vis des acides aminés par la RMNIn situ : études de radicaux issus de ces composés sur des épidermes humains reconstitués par RPEIn cellulo : étude du stress oxydant sur les cellules dendritiques et la voie de signalisation Keap1/Nrf2/ARE. / Allergic contact dermatitis is a pathology affecting 15 to 20% of the Western population. Until now no treatment exists, the prevention is the eviction of allergens. In the past, tests concerning new molecules for the market were tested on animals until the prohibition in the 7th amendment of the European directive concerning the cosmetics industry. In this context it is essential to develop alternative methods to assess the allergenic potential of chemicals.This manuscript proposes to analyze the problem of the allergic contact dermatitis from the molecule to the tissue for allergens reacting through radical mechanisms:In chemico: study of the reactivity profile of allylic hydroperoxides toward amino acids by NMRIn situ: radical intermediates formation on reconstructed human epidermis from allylic hydroperoxides by EPR In cellulo: study of the oxidative stress from allylic hydroperoxides on dendritic cells trough the Keap1/Nrf2/ARE sensor pathway.

p. 1-157 / Submitted by Santiago Fabio (fabio.ssantiago@hotmail.com) on 2013-04-24T21:12:07Z No. of bitstreams: 1 22222222222tttt.pdf: 2420212 bytes, checksum: d208a267b6fe5b14ae33b31fc9319a4a (MD5) / Approved for entry into archive by Maria Creuza Silva(mariakreuza@yahoo.com.br) on 2013-05-04T17:08:10Z (GMT) No. of bitstreams: 1 22222222222tttt.pdf: 2420212 bytes, checksum: d208a267b6fe5b14ae33b31fc9319a4a (MD5) / Made available in DSpace on 2013-05-04T17:08:10Z (GMT). No. of bitstreams: 1 22222222222tttt.pdf: 2420212 bytes, checksum: d208a267b6fe5b14ae33b31fc9319a4a (MD5) Previous issue date: 2011 / O objetivo deste estudo foi investigar a influência de fatores ambientais, antropométricos e de estilo de vida em asma e atopia em uma área rural do Equador. Foi conduzido um estudo transversal, a partir do qual foram identificadas crianças e adolescentes, com e sem chiado no peito no ultimo ano, para serem incluídas no estudo caso-controle. Inicialmente, um estudo exploratório foi realizado para identificar se diferentes fatores (sócioeconômicos, ambientais, famíliares, estilo de vida, infecção por helmintos) estariam associados com sibilo atópico e não-atópico na área rural. Os resultados mostraram que sibilo não-atópico foi o fenótipo mais comum nesta área, e foi observado um padrão diferente de fatores de risco para sibilância atópica e não-atópica, o que pode sugerir que diferentes mecanismos podem estar envolvidos. Vários estudos nas áreas rurais e urbanas pobres na América Latina têm reportado que a asma não é atribuída a atopia. Da mesma forma, uma dissociação entre a IgE específica e reatividade ao teste cutâneo tem sido observada. Assim, testamos a hipótese de que na nossa população, infecções por helmintos, poderiam estar modificando estas associações. Os resultados mostram uma relação complexa entre helmintos, asma e atopia. Notou-se que a associação entre os marcadores de atopia foi mais débil nos indivíduos com presença de sensibilização para Ascaris, e a associação entre o teste cutâneo e sibilo, foi atenuada em indivíduos com infecção ativa com Ascaris e / ou Trichuris. Adicionalmente a IgE anti-Ascaris, mas não infecção ativa, incrementou o risco de sibilo, independentemente de IgE específica a alérgenos. Finalmente, uma nova hipótese sugere que a adoção de novos estilos de vida estaria conduzindo a um aumento da asma e atopia. Assim, estudou-se excesso de peso, por ser considerado um marcador de recentes mudanças nos padrões de vida e que, por sua vez, estaria associado com asma e atopia. A presença de teste cutâneo e IgE específica a alérgenos foi de 1,85 e 2,20 vezes maior em crianças com excesso de peso do que em crianças eutróficas/déficit, respectivamente. No entanto, o efeito em sibilo foi decorrente de um mecanismo não-atópico. Embora esses resultados precisem ser confirmados por estudos longitudinais, certamente contribuirão para uma melhor compreensão dos mecanismos da asma não-atopica nas aéreas rurais, que tem sido muito pouco compreendidos. / Salvador