Urticaria is a common skin disorder that is classified according to its chronicity into acute and chronic forms. It may occur spontaneously or on exposure to a physical factor. In the latter case, the urticaria is classified as a physical urticaria. Physical urticaria may be induced by mechanical and applied pressure, exercise, or exposure to cold, heat, sun, water, or vibration. The urticarial lesions are generally thought to be the result of mast cell activation and degranulation, which is supported by the finding of increased levels of serum histamine during some urticarial flares. Passive transfer experiments, whereupon serum from affected donors is transferred into recipients'skin followed by physical stimulation with resultant urticaria at the site of challenge, have been positive in some instances. This suggests the presence of an intrinsic factor in serum, such as IgE, which then mediates activation of tissue mast cells. However, the pathogenesis in general remains unclear and a genetic basis for these disorders has not been elucidated. The purpose of this protocol is to investigate the pathogenic mechanisms of physical urticaria and provide further characterization of the various clinical subtypes. Both adult and pediatric patients undergo standard challenge testing to verify their urticaria. Blood samples are obtained for the investigation of molecular and genetic pathways involved in the disease process. Following the clinical induction of urticarial manifestations, additional blood samples are collected to determine molecular and genetic changes. Photographic imaging studies may be done during challenge testing. Skin biopsies may be obtained prior to and following challenge testing that are analyzed for biochemical and histological markers. Patients receive counseling regarding appropriate management of their disease and may be scheduled for a return visit to provide additional samples and for longitudinal analysis of their disease manifestations. Blood and tissue may be stored for future studies. Since the inception of our protocol in June 2009 we have enrolled 26 patients (4 are control patients) with over 50 total patient visits. All patients underwent challenge testing based on their history. Blood samples and, in some cases, skin biopsies have been collected and stored for biochemical, molecular and when applicable, genetic analysis. The majority of the patients were challenge positive to either cold-induced, cholinergic, dermatographism, solar or vibratory urticaria.

Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
2010
Total Cost
$121,603
Indirect Cost
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State
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Zip Code
Valent, Peter; Akin, Cem; Bonadonna, Patrizia et al. (2018) Mast cell activation syndrome: Importance of consensus criteria and call for research. J Allergy Clin Immunol 142:1008-1010
Hanjra, Pahul; Lee, Chyi-Chia R; Maric, Irina et al. (2018) Chromogranin A is not a biomarker of mastocytosis. J Allergy Clin Immunol Pract 6:687-689.e4
Boyden, Steven E; Metcalfe, Dean D; Komarow, Hirsh D (2016) Vibratory Urticaria and ADGRE2. N Engl J Med 375:95
Kirshenbaum, Arnold S; Cruse, Glenn; Desai, Avanti et al. (2016) Immunophenotypic and Ultrastructural Analysis of Mast Cells in Hermansky-Pudlak Syndrome Type-1: A Possible Connection to Pulmonary Fibrosis. PLoS One 11:e0159177
Boyden, Steven E; Desai, Avanti; Cruse, Glenn et al. (2016) Vibratory Urticaria Associated with a Missense Variant in ADGRE2. N Engl J Med 374:656-63
Hox, Valerie; Desai, Avanti; Bandara, Geethani et al. (2015) Estrogen increases the severity of anaphylaxis in female mice through enhanced endothelial nitric oxide synthase expression and nitric oxide production. J Allergy Clin Immunol 135:729-36.e5
Komarow, Hirsh D; Eisch, A Robin; Young, Michael et al. (2015) Solar Urticaria. J Allergy Clin Immunol Pract 3:789-90
Komarow, Hirsh D; Sokolic, Robert; Hershfield, Michael S et al. (2015) Impulse oscillometry identifies peripheral airway dysfunction in children with adenosine deaminase deficiency. Orphanet J Rare Dis 10:159
Williams, Kelli W; Metcalfe, Dean D; Prussin, Calman et al. (2014) Telangiectasia macularis eruptiva perstans or highly vascularized urticaria pigmentosa? J Allergy Clin Immunol Pract 2:813-5
Carter, Melody C; Metcalfe, Dean D; Komarow, Hirsh D (2014) Mastocytosis. Immunol Allergy Clin North Am 34:181-96

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