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1.
Int Arch Allergy Immunol ; 178(4): 370-376, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-30677773

RESUMO

BACKGROUND: Peanut storage proteins (Ara h 1, Ara h 2, and Ara h 3) have been described as the major peanut allergens in children, although not all peanut-sensitized individuals have clinical reactivity after exposure. OBJECTIVES: We studied the sensitization profile of peanut-allergic and peanut-tolerant children in a pediatric cohort. METHODS: The clinical features and sensitization profile to the peanut storage proteins Ara h 9 and Pru p 3 were compared between peanut-allergic and peanut-tolerant children using component-resolved diagnostics. RESULTS: Thirty-three peanut-sensitized children were included: 22 allergic and 11 tolerant patients. Seventy-two percent of the peanut-allergic children were sensitized to at least one peanut storage protein. The rates of sensitization to Ara h 1, Ara h 2, and Ara h 3 were 63.6, 68.1, and 68.1%, respectively, among the peanut-allergic children and 27.2, 18.1, and 45.4% among the peanut-tolerant children. IgE from the sera of 18% of the peanut-allergic patients recognized Ara h 9, whereas no sensitization to Ara h 9 was detected in the peanut-tolerant children. A total of 59% of the peanut-allergic and 27% of the peanut-tolerant children were sensitized to Pru p 3. Sensitization to Ara h 1 and Ara h 2 was more frequent among the peanut-allergic children (p < 0.05). Although the levels of specific IgE against peanut storage proteins were higher in peanut allergy, there were not statistically significantly different from the levels in peanut tolerance, probably due to the small number of patients included. CONCLUSIONS: In our population, the peanut-allergic children were mainly sensitized to peanut storage proteins, and Ara h 2 sensitization allows a more accurate diagnosis of clinical reactivity to peanuts. More than half of the peanut-allergic patients were sensitized to peach Pru p 3, and 50% of them had fruit allergy at the time of the study.


Assuntos
Tolerância Imunológica , Hipersensibilidade a Amendoim/imunologia , Albuminas 2S de Plantas/imunologia , Adolescente , Antígenos de Plantas/imunologia , Criança , Pré-Escolar , Feminino , Glicoproteínas/imunologia , Humanos , Imunoglobulina E/sangue , Masculino , Proteínas de Plantas/imunologia
2.
Am J Med ; 130(9): 1114-1116, 2017 09.
Artigo em Inglês | MEDLINE | ID: mdl-28601540

RESUMO

BACKGROUND: The relationship between anaphylaxis and cardiovascular events has been reported in the past. While skin and respiratory symptoms are usually the most common and the first to appear, cardiovascular complications play a key role and represent the leading cause of death in anaphylaxis. METHODS: We report 3 episodes of atrial fibrillation triggered by anaphylaxis. Allergy and cardiology studies were performed. In both patients, the etiological agent was identified: Anisakis simplex hypersensitivity and food allergy. RESULTS: The heart is the source and target of chemical mediators released during an allergic reaction. In the heart, there are plenty of mast cells, and they are predominantly located around the coronary adventitia and in close contact with small vessels in the muscle wall. The release of mediators can influence ventricular function, heart rate, and coronary artery tone. Anaphylaxis can trigger any kind of arrhythmia. In these cases, the very interesting point of discussion was: which should be first, treating anaphylaxis or cardiac events? The other controversial point was the use of epinephrine, the first line of treatment for anaphylaxis. Recommendations about epinephrine in cardiac patients during an anaphylactic event are still a major dilemma. CONCLUSIONS: We emphasize the importance of the priority of establishing protocols between cardiologist and allergist in treatment of cardiac complications during anaphylaxis, and we warn about the correct diagnosis of arrhythmias in anaphylaxis in order to treat them as soon as possible, to prevent other consequences and complications.


Assuntos
Anafilaxia/complicações , Atenolol/administração & dosagem , Fibrilação Atrial/etiologia , Clorfeniramina/administração & dosagem , Epinefrina/uso terapêutico , Hipersensibilidade Alimentar/complicações , Metilprednisolona/uso terapêutico , Urticária/complicações , Actinidia/efeitos adversos , Actinidia/imunologia , Administração Intravenosa , Adulto , Idoso de 80 Anos ou mais , Anafilaxia/tratamento farmacológico , Anafilaxia/etiologia , Animais , Anisakis/imunologia , Anisakis/parasitologia , Antiarrítmicos/administração & dosagem , Antiarrítmicos/imunologia , Antiarrítmicos/uso terapêutico , Anti-Inflamatórios/administração & dosagem , Anti-Inflamatórios/uso terapêutico , Arachis/efeitos adversos , Arachis/imunologia , Atenolol/imunologia , Atenolol/uso terapêutico , Fibrilação Atrial/tratamento farmacológico , Broncodilatadores/administração & dosagem , Broncodilatadores/uso terapêutico , Clorfeniramina/uso terapêutico , Quimioterapia Combinada , Epinefrina/administração & dosagem , Hipersensibilidade Alimentar/diagnóstico , Hipersensibilidade Alimentar/tratamento farmacológico , Hipersensibilidade Alimentar/etiologia , Gadiformes/imunologia , Gadiformes/parasitologia , Antagonistas dos Receptores Histamínicos H1/administração & dosagem , Antagonistas dos Receptores Histamínicos H1/uso terapêutico , Humanos , Hipodermóclise , Masculino , Metilprednisolona/administração & dosagem , Urticária/etiologia , Urticária/imunologia
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