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1.
Ann Allergy Asthma Immunol ; 128(2): 206-212, 2022 02.
Article in English | MEDLINE | ID: mdl-34737038

ABSTRACT

BACKGROUND: The prevalence of sesame allergy is increasing; strict avoidance is the mainstay of therapy. Lately, sesame oral immunotherapy was presented as an alternative treatment, with a high rate of success. Therefore, data on the natural history and the clinical characteristics of patients with persistent sesame allergy are important for the management of patients with sesame allergy. OBJECTIVE: To describe the natural history of patients with sesame allergy and the clinical characteristics of patients with spontaneous resolution of sesame allergy compared with patients with persistent sesame allergy. METHODS: In our retrospective study, electronic health records of patients with sesame allergy diagnosis were reviewed for demographic and clinical data. Statistical analysis of clinical characteristics of patients with spontaneous resolution compared with persistent sesame allergy was performed. RESULTS: A total of 190 patients with sesame allergy were followed for 3.86 ±4.43 years. Of these patients, 61 (32.1%) had spontaneous resolution of sesame allergy. Patients with mild, early (before the age of 10 months) first sesame allergic reaction, with smaller than 7-mm skin prick test and without concomitant tree nut allergy had better resolution rate (56.1%). CONCLUSION: Sesame allergy spontaneously resolved in approximately one-third of our patients and in more than half of the patients with mild first reaction (grade 1) at a young age (<10 months), with small skin prick test (<7 mm) and no concomitant tree nut allergy. Larger prospective studies with longer follow-up period are needed to better characterize the sesame allergic patients with persistent allergy who may need oral immunotherapy.


Subject(s)
Food Hypersensitivity , Nut Hypersensitivity , Sesamum , Allergens , Humans , Infant , Prospective Studies , Retrospective Studies , Skin Tests
2.
Clin Exp Pharmacol Physiol ; 44 Suppl 1: 64-69, 2017 12.
Article in English | MEDLINE | ID: mdl-28466565

ABSTRACT

Aging is associated with altered decreased barrier function in the skin, which can lead to different types of immunoglobulin E (IgE)-mediated sensitization to environmental allergens. Yet, allergen-specific respiratory sensitization among the elderly is not well described. The aim of this study was to investigate the effect of aging on allergic pulmonary inflammation induced by epicutaneous sensitization of mechanically irritated skin in mice. For this purpose, 6-week-, 6-month-, and 18-month-old female BALB/c mice, underwent epicutaneous sensitization with ovalbumin (OVA) or phosphate buffered saline (PBS), followed by an inhaled OVA challenge. Blood OVA-specific IgE levels measured after epicutaneous sensitization, as well as, bronchial alveolar lavage fluids (BALF) leucocyte, eosinophil, and cytokine levels measured after OVA inhalation challenge were similar among the 6-week-old (young) and 6-month-old (adult) groups. However, significantly decreased levels of systemic OVA IgE, and BALF leukocyte, eosinophil and T helper cell type 2 cytokine levels, were measured after OVA inhalation challenge in elderly (18-month-old) mice compared to the other groups of mice. In addition, interleukin-10 (IL-10), a regulatory suppressor cytokine, was more abundant in the BALF of the elderly group after epicutaneous sensitization and inhalation challenge. Our results suggest that elderly mice have a reduced allergic response to induced sensitization with OVA, possibly regulated by increased IL-10 levels.


Subject(s)
Aging/immunology , Lung/immunology , Ovalbumin/administration & dosage , Pneumonia/prevention & control , Respiratory Hypersensitivity/prevention & control , Skin/immunology , Administration, Cutaneous , Age Factors , Animals , Bronchoalveolar Lavage Fluid/immunology , Disease Models, Animal , Eosinophils/immunology , Eosinophils/metabolism , Female , Immunoglobulin E/blood , Immunoglobulin E/immunology , Interleukin-10/immunology , Interleukin-10/metabolism , Lung/metabolism , Mice, Inbred BALB C , Ovalbumin/immunology , Pneumonia/blood , Pneumonia/immunology , Respiratory Hypersensitivity/blood , Respiratory Hypersensitivity/immunology , Skin/metabolism , Th2 Cells/immunology , Th2 Cells/metabolism
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