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2.
J Investig Allergol Clin Immunol ; 32(1): 1-12, 2022 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-35188463

RESUMO

Considerable progress has been made in the field of molecular biology in recent years, enabling the study of sensitization to the individual components of an allergenic source, a practice that has been termed molecular allergy diagnosis (MD) or component-resolved diagnosis (CRD). The present review provides the clinician with a practical approach to the use of MD by answering questions frequently asked by physicians on how MD can help improve the diagnosis of allergy in daily clinical practice. The article is divided into 3 sections. First, we provide a brief review of the importance for the clinician of knowing the main allergens in the different allergenic sources, their structure, and their in vitro cross-reactivity before approaching MD (section A). Second, we review the usefulness of MD in clinical practice (section B) and answer frequently asked questions on the subject. Finally, section C addresses the interpretation of MD and its integration with other tools available for the diagnosis of allergy.


Assuntos
Hipersensibilidade , Alérgenos , Reações Cruzadas , Humanos , Hipersensibilidade/diagnóstico
6.
Allergol Immunopathol (Madr) ; 45(1): 48-54, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-27592278

RESUMO

BACKGROUND: Food allergy affects around 6% of the European population and its prevalence worldwide has been increasing in the last decades, but studies focused on investigating food allergy epidemiology in Europe are lacking. OBJECTIVE: The Cibus project was created to register the main culprit foods and their clinical manifestations in food allergic patients in Catalonia. METHODS: A specific online database was designed. Allergists from eight different Catalan hospitals registered the new diagnoses of food allergy. RESULTS: 618 food allergic patients were included. Egg and milk were the main elicitors in the early ages, while fruits and nuts were the most frequent in patients >14 years old. Fish was more frequent in children, while seafood and Anisakis allergy were more frequent in the >14-year-old group. Overall, peach was the most prevalent food eliciting an allergic reaction (10%). Food allergy diagnosis was reached using compatible clinical history and positive skin prick test to the involved food in 98% of cases. Globally, urticaria was the most frequently reported manifestation in our population (48.2%), followed by oral allergy syndrome (25.6%) and anaphylaxis (24.8%). CONCLUSIONS: The Cibus project gives a full overview of the profile of food allergic patients in Catalonia and reinforces the predominance of plant food allergies in the Mediterranean area.


Assuntos
Hipersensibilidade Alimentar/epidemiologia , Adolescente , Adulto , Alérgenos/imunologia , Criança , Reações Cruzadas , Estudos Transversais , Feminino , Humanos , Masculino , Material Particulado/imunologia , Prevalência , Testes Cutâneos , Espanha/epidemiologia , Adulto Jovem
7.
Allergy ; 72(1): 35-42, 2017 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-27439141

RESUMO

Allergic rhinitis and asthma constitute two clinical expressions of a single-condition, respiratory allergy. Allergen immunotherapy (AIT) is a form of treatment specifically aimed at modifying the response to sensitizing allergens. The inherent potential benefit of AIT is the simultaneous treatment of all clinical expressions of respiratory allergy. Current data support the effectiveness of subcutaneous and sublingual immunotherapy in rhinitis. Studies also provide proof for a beneficial effect in allergic asthma. Even more, substantial evidence points to the preventive effect on the progression from rhinitis to asthma. Despite the current knowledge on the basic mechanisms underlying the immunological effect of AIT is vast, the specific mechanisms for the preventive effect of primary sensitization or new sensitizations are poorly understood. This review aimed to provide a critical overview of the current knowledge on the effectiveness of AIT and its potential role in secondary prevention of respiratory allergy progression.


Assuntos
Imunoterapia , Rinite Alérgica/imunologia , Rinite Alérgica/terapia , Alérgenos/imunologia , Asma/epidemiologia , Asma/etiologia , Asma/patologia , Dessensibilização Imunológica/efeitos adversos , Dessensibilização Imunológica/métodos , Progressão da Doença , Humanos , Imunoterapia/efeitos adversos , Imunoterapia/métodos , Rinite Alérgica/epidemiologia , Rinite Alérgica/prevenção & controle , Resultado do Tratamento
8.
Allergy ; 67(10): 1316-8, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22845005

RESUMO

BACKGROUND: Alcohol, exercise or non-steroidal anti-inflamatory drugs (NSAID) are frequently mentioned as amplifiers of food allergic reactions but only individual cases or small series have been previously published. METHODS: Descriptive study including 74 cases of suspected co-factor enhanced food allergy, assessed by skin-prick tests, specific IgE and oral challenges. RESULTS: Anaphylaxis accounted for 85.1% of reactions. In 99% of cases culprit food allergens were plant-derived, mainly vegetables and cereals. NSAID were involved in 58%, exercise in 52.7% and alcohol in 12.2%. Lipid transfer protein was the most frequently involved allergen. CONCLUSIONS: Co-factor enhanced food allergy should be considered when assessing food, alcohol, exercise and NSAID allergic reactions.


Assuntos
Alérgenos/efeitos adversos , Anafilaxia , Anti-Inflamatórios não Esteroides/efeitos adversos , Exercício Físico , Hipersensibilidade Alimentar , Proteínas de Plantas/efeitos adversos , Adulto , Alérgenos/imunologia , Anafilaxia/etiologia , Anafilaxia/imunologia , Anti-Inflamatórios não Esteroides/imunologia , Proteínas de Transporte/efeitos adversos , Proteínas de Transporte/imunologia , Hipersensibilidade Alimentar/etiologia , Hipersensibilidade Alimentar/imunologia , Humanos , Imunoglobulina E/sangue , Proteínas de Plantas/imunologia , Testes Cutâneos
9.
An Pediatr (Barc) ; 76(3): 133-9, 2012 Mar.
Artigo em Espanhol | MEDLINE | ID: mdl-22047794

RESUMO

OBJECTIVES: To determine the prevalence of homocystinuria in Spain and to establish the measures and mechanisms to ensure its prevention, diagnosis and treatment. MATERIAL AND METHODS: A national cross-sectional survey was conducted by means of a questionnaire sent to 35 hospitals in which children and adult patients are treated. RESULTS: Using the questionnaires submitted by 25 physicians from 16 centres, 75 patients were identified: 41 transsulphuration defects (one deceased), 27 remethylation (six deaths) and 7 without a syndromic diagnosis. The age at diagnosis varied widely, and 18 cases had more than one sibling affected. The more severe clinical manifestations involved the patients with remethylation defects. There was a high percentage of cognitive impairment, followed by lens diseases. Almost half of the patients had neurological disorders. There was increased vascular involvement in CBS-deficient adults. The therapeutic options most used were, folic acid, hydroxycobalamin and betaine. CONCLUSIONS: In view of these results and especially the small number of CBS deficiencies detected, we conclude that there is a need to introduce newborn screening for classical homocystinuria and ensure implementation of an appropriate diagnostic workup in all patients at risk.


Assuntos
Homocistinúria/epidemiologia , Adolescente , Criança , Pré-Escolar , Estudos Transversais , Feminino , Homocistinúria/diagnóstico , Homocistinúria/etiologia , Homocistinúria/terapia , Humanos , Incidência , Lactente , Recém-Nascido , Masculino , Doenças Metabólicas/complicações , Prevalência , Espanha
11.
Clin Exp Allergy ; 38(6): 1048-60, 2008 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-18489028

RESUMO

BACKGROUND: The genus Senecio is the largest genus of the family Asteraceae (Compositae). The allergenicity of Senecio has not been assessed previously. OBJECTIVE: The aim of this study was to investigate the allergens of Senecio jacobea pollen and to determine their immunological characteristics and clinical relevance. METHODS: Fifty patients with rhinoconjunctivitis and a positive skin prick test (SPT) to Senecio were recruited. The clinical relevance of this pollen was assessed by means of a nasal provocation test (NPT). Allergens were characterized by one-dimensional electrophoresis (SDS-PAGE) and two-dimensional gel electrophoresis and immunoblotting. Furthermore, characterization and identification of the allergens were performed by mass spectrometry (MS). In vitro inhibition tests were performed to evaluate cross-reactivity with other pollen. RESULTS: Three predominant allergens, both in the intensity of reaction and the frequency of recognition by human-allergic sera, were 59 (60%), 42 (50%) and 31 kDa (50%). The two-dimensional analysis allowed the identification of several allergens. One spot around 42 kDa was identified as a protein homologous to pectate lyase and three other spots were homologous to malate dehydrogenase by MS. S. jacobea proteins showed cross-reactivity with other proteins of the Asteraceae family and also with Parietaria judaica. This was demonstrated by immunoblotting and ELISA inhibition studies. CONCLUSION: S. jacobea constitute a newly discovered allergenic source. It shows cross-reactivity with other members of the Asteraceae plant family as well as with P. judaica.


Assuntos
Alérgenos/imunologia , Proteínas de Plantas/imunologia , Pólen/imunologia , Rinite Alérgica Sazonal/etiologia , Senécio/imunologia , Adolescente , Adulto , Idoso , Alérgenos/efeitos adversos , Alérgenos/análise , Animais , Asteraceae/efeitos adversos , Asteraceae/imunologia , Gatos , Reações Cruzadas , Cães , Eletroforese/métodos , Feminino , Humanos , Imunoensaio , Imunoglobulina E/sangue , Imunoglobulina E/imunologia , Exposição por Inalação , Masculino , Espectrometria de Massas , Pessoa de Meia-Idade , Testes de Provocação Nasal , Parietaria/efeitos adversos , Parietaria/imunologia , Proteínas de Plantas/efeitos adversos , Proteínas de Plantas/análise , Pólen/efeitos adversos , Rinite Alérgica Sazonal/diagnóstico , Rinite Alérgica Sazonal/imunologia , Senécio/efeitos adversos , Testes Cutâneos
12.
J Investig Allergol Clin Immunol ; 18(2): 126-30, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18447143

RESUMO

Angioedema caused by C1 inhibitor deficiency is a rare disorder that may be either hereditary or acquired, the latter being mainly associated with lymphoproliferative disorders. A 51-year-old woman who had suffered from episodes of acute peripheral edema since she was 12 was diagnosed with hereditary angioedema at the age of 40 and remained stable with stanozolol. Due to a worsening of her symptoms she was reassessed and low levels of C1q and an abnormal lymphocyte count were detected. Immunophenotyping of peripheral blood revealed 9% monoclonal lambda B cells with a follicular center phenotype. The histopathology was consistent with a grade II follicular lymphoma stage IV-A.With chemotherapy, the hematologic disease was controlled and C1q levels returned to normal values. This represents a rare case of a patient with hereditary angioedema who developed acquired angioedema due to a lymphoma that was associated with a reduction in the levels of C1q as her symptoms worsened.


Assuntos
Angioedema/etiologia , Angioedemas Hereditários/complicações , Proteínas Inativadoras do Complemento 1/deficiência , Linfoma Folicular/etiologia , Angioedemas Hereditários/sangue , Angioedemas Hereditários/tratamento farmacológico , Angioedemas Hereditários/imunologia , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Ativação do Complemento , Complemento C1/genética , Complemento C1/metabolismo , Proteínas Inativadoras do Complemento 1/genética , Proteínas Inativadoras do Complemento 1/imunologia , Proteína Inibidora do Complemento C1 , Feminino , Humanos , Contagem de Linfócitos , Linfoma Folicular/tratamento farmacológico , Pessoa de Meia-Idade , Linhagem , Estanozolol/uso terapêutico
13.
Rev Neurol ; 30(1): 48-50, 2000.
Artigo em Espanhol | MEDLINE | ID: mdl-10742996

RESUMO

INTRODUCTION: Miller-Dieker syndrome is characterized for type 1 lissencephaly associated with facial dysmorphism. In 90-95% of the cases, deletion of the distal fragment of chromosome 17 is seen. Nevertheless, this is difficult to confirm in about 50% of the cases, if we don't resort to special technics of molecular genetics. CLINICAL CASE: We show a 3 years old patient diagnosed of lissencephaly and with peculiar facial features in whom the cytogenetic study was normal, but by in situ hybridization deletion of 17p13.3 fragment was showed. CONCLUSION: We want to emphasize the ultrasonography findings and we want to suggest this easy imaging method and useful technic in the study of neuronal migrational disorders.


Assuntos
Encefalopatias/diagnóstico , Encéfalo/anormalidades , Ecoencefalografia/métodos , Anticonvulsivantes/uso terapêutico , Encefalopatias/genética , Pré-Escolar , Deleção Cromossômica , Cromossomos Humanos Par 17/genética , Epilepsia/diagnóstico , Epilepsia/tratamento farmacológico , Feminino , Humanos , Imageamento por Ressonância Magnética , Síndrome
15.
An Esp Pediatr ; 29(2): 153-6, 1988 Aug.
Artigo em Espanhol | MEDLINE | ID: mdl-3056151

RESUMO

Authors present two cases of calcification of the intervertebral disc. They provide an analysis of etiology, symptoms, and roentgenographic clinic course, as well as a review of cases which have been reported in literature.


Assuntos
Calcinose/diagnóstico por imagem , Disco Intervertebral , Doenças da Coluna Vertebral/diagnóstico por imagem , Calcinose/etiologia , Pré-Escolar , Feminino , Humanos , Masculino , Radiografia , Doenças da Coluna Vertebral/etiologia
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