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Medicinas Complementárias
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1.
Allergy ; 72(4): 562-569, 2017 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-27588729

RESUMEN

BACKGROUND: Overlapping seasons and cross-reactivity, especially to grass pollen profilin, can hamper the diagnosis of birch pollen allergy. To identify the primary sensitizing allergen and the clinical relevance of cross-sensitization, we correlated sensitization profiles with in vitro and in vivo tests, symptom scores, and pollen counts. METHODS: A total of 433 patients with positive skin prick test (SPT) to birch pollen were analyzed regarding IgE to major birch and grass pollen allergens Bet v 1 and Phl p 1/p 5 and the profilins Bet v 2 and Phl p 12. Subgroups were analyzed by basophil activation test (BAT) and CAP-FEIA-based cross- and self-inhibition tests. RESULTS: A total of 349 patients were sensitized to Bet v 1, 44 patients to both Bet v 1 and Bet v 2, and 15 patients to Bet v 2 only. From Bet v 2-sensitized patients, 40 were also sensitized to Phl p 12. Ex vivo, Bet v 2 and Phl p 12 induced dose-dependent activation in basophils of these patients. Cross- and self-inhibition tests with both allergens confirmed cross-reactivity. However, semiquantitative analysis of SPTs demonstrated markedly increased reactivity to grass compared to birch pollen extract in Bet v 2 only sensitized patients. Accordingly, in most of those patients, clinical symptoms precisely correlated with grass pollen counts. CONCLUSION: Identification of the clinically relevant and sensitizing allergen needs correlation of actual pollen counts with clinical symptoms and sensitization status to major allergens. Semiquantitative analysis of SPT or BAT and determining profilin-specific IgE can contribute to making the diagnosis.


Asunto(s)
Alérgenos/inmunología , Betula/inmunología , Reacciones Cruzadas/inmunología , Polen/inmunología , Profilinas/inmunología , Rinitis Alérgica Estacional/diagnóstico , Rinitis Alérgica Estacional/inmunología , Adolescente , Adulto , Especificidad de Anticuerpos/inmunología , Basófilos/inmunología , Basófilos/metabolismo , Femenino , Humanos , Inmunización , Inmunoglobulina E/sangre , Inmunoglobulina E/inmunología , Recuento de Leucocitos , Masculino , Rinitis Alérgica Estacional/sangre , Pruebas Cutáneas , Adulto Joven
2.
J Eur Acad Dermatol Venereol ; 29(12): 2399-404, 2015 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-26304054

RESUMEN

BACKGROUND: The prognostic and therapeutic features of scleredema are poorly documented. OBJECTIVES: To describe the characteristics of patients with scleredema regarding demographics, clinical characteristics, comorbidities, therapeutic interventions and course. METHODS: We conducted a retrospective multicentre study. RESULTS: We identified 44 patients (26 men).The mean age at diagnosis was 53.8 years. The most common associated disorders were endocrine/metabolic diseases including 30 patients suffering from diabetes, mostly type 2 diabetes. Monoclonal gammopathies were confirmed in five cases. A preceding respiratory tract infection was not a feature. Treatments with different combination or sequential modalities were used with variable results. Phototherapy (UVA1 or PUVA) was the treatment associated with higher, although partial response. Systemic corticosteroids and immunosuppressive drugs were reserved to patients with severe disease in whom phototherapy had failed or for patients with multiple myeloma. Forty-one patients were followed up (mean period: 32.2 months).Thirty-nine patients are alive, 30 with and 9 without skin disease. Two patients died of cardiovascular complications due to myeloma and severe diabetes. CONCLUSIONS: Scleredema is a chronic debilitating disease associated with diabetes and metabolic syndrome, unresponsive to various treatments but not necessarily a life-threatening condition. Although there is no definitive treatment, phototherapy should be attempted first. Treatment of primary disease including strict glycaemic control combined with physical therapy should be also employed.


Asunto(s)
Diabetes Mellitus Tipo 2/epidemiología , Terapia PUVA , Paraproteinemias/epidemiología , Escleredema del Adulto/tratamiento farmacológico , Escleredema del Adulto/epidemiología , Corticoesteroides/uso terapéutico , Adulto , Anciano , Comorbilidad , Dislipidemias/epidemiología , Femenino , Humanos , Inmunosupresores/uso terapéutico , Masculino , Persona de Mediana Edad , Obesidad/epidemiología , Estudios Retrospectivos , Tasa de Supervivencia , Adulto Joven
3.
Klin Padiatr ; 223(6): 364-7, 2011 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-22052633

RESUMEN

A 12-year old girl presented with general weakness and weight loss, a localised cervical lymph node enlargement and cutaneous lesions compatible with lymphomatoid papulosis (LyP). Biopsies from lymph node and skin revealed a histological diagnosis of nodal large cell ALK-1- anaplastic lymphoma (ALCL) with a synchronous CD30+ cutaneous lymphoproliferation consistent with lymphomatoid papulosis (LyP). The girl was treated with mistletoe (MT) as monotherapy. Within 1 week after initiation of MT-treatment the skin lesions and lymph node enlargement improved. Under continuing MT-therapy 30 months after diagnosis the patient is still in complete remission. It is not possible to know whether this was a rare case of spontaneous remission of the nodal and skin-manifestations of this CD30+ T-cell lymphoproliferation or whether the observed effect was a specific therapeutic response to MT-treatment.


Asunto(s)
Receptores de Activinas Tipo II/análisis , Linfoma Anaplásico de Células Grandes/tratamiento farmacológico , Papulosis Linfomatoide/tratamiento farmacológico , Muérdago , Fitoterapia , Extractos Vegetales/uso terapéutico , Inducción de Remisión , Neoplasias Cutáneas/tratamiento farmacológico , Niño , Femenino , Estudios de Seguimiento , Humanos , Ganglios Linfáticos/patología , Linfoma Anaplásico de Células Grandes/diagnóstico , Neoplasias Cutáneas/diagnóstico
5.
Allergy ; 59(5): 526-32, 2004 May.
Artículo en Inglés | MEDLINE | ID: mdl-15080834

RESUMEN

BACKGROUND: To date, very little data are available about the nature of tomato allergens. Immunoglobulin E (IgE) cross-reactive profilins have been suggested to account for allergic symptoms in patients suffering from tomato allergy. METHODS: The cDNA of tomato profilin was amplified by reversely transcribed polymerase chain reaction (RT-PCR) from total RNA extracted from ripe tomato fruit. The gene was cloned into the pET101D expression plasmid and the protein was produced in Escherichia coli BL21. Purification was performed via poly-l-proline (PLP) affinity chromatography. IgE reactivity of recombinant tomato profilin was investigated by immunoblot and enzyme-linked immunosorbent assay. IgE-inhibition studies were performed to analyse cross-reactivity with other profilins. To determine the allergenic activity of the recombinant protein, basophil histamine release assays using sera of patients with adverse reactions to tomato were performed. RESULTS: Profilin was identified as a new minor allergen in tomato fruits. The recombinant tomato profilin comprises 131 amino acids and high sequence identity to other allergenic food and pollen profilins. It was shown to be IgE-reactive with a prevalence of 22% (11/50) in tomato-allergic patients. In patients with tomato allergy and multiple sensitization to other foods and birch pollen, IgE directed against tomato profilin showed a strong cross-reactivity with profilins from plant food sources and birch pollen. The tomato profilin was able to induce mediator release from human basophils. CONCLUSION: The tomato profilin is a minor allergen in tomato fruit. Thus, it shows biological activity, as confirmed by in vitro histamine release assays with human basophils and thereby has the potential to account for clinical symptoms in tomato-allergic patients.


Asunto(s)
Alérgenos/inmunología , Proteínas Contráctiles/inmunología , Hipersensibilidad a los Alimentos/etiología , Hipersensibilidad a los Alimentos/inmunología , Inmunoglobulina E/inmunología , Proteínas de Microfilamentos/inmunología , Solanum lycopersicum/efectos adversos , Solanum lycopersicum/inmunología , Adulto , Alérgenos/genética , Alérgenos/metabolismo , Secuencia de Aminoácidos , Antígenos de Plantas , Basófilos/metabolismo , Betula/inmunología , Clonación Molecular , Proteínas Contráctiles/genética , Proteínas Contráctiles/metabolismo , Reacciones Cruzadas , ADN Complementario , Escherichia coli/metabolismo , Femenino , Liberación de Histamina , Humanos , Inmunización , Masculino , Proteínas de Microfilamentos/genética , Proteínas de Microfilamentos/metabolismo , Persona de Mediana Edad , Datos de Secuencia Molecular , Polen/inmunología , Profilinas , Proteínas Recombinantes/inmunología
6.
Hautarzt ; 52(10 Pt 2): 985-8, 2001 Oct.
Artículo en Alemán | MEDLINE | ID: mdl-11715400

RESUMEN

Granulomatous slack skin (GSS) is a rare cutaneous T-cell lymphoma which typically runs a protracted and indolent course. On histopathological assessment lymphoid infiltrates with multinucleated giant cells in the dermis and subcutis with elastophagocytosis can be observed. Skin lesions are characterized by pendulous folds. We report on the successful response of the lesions to intralesional interferon alpha combined with PUVA.


Asunto(s)
Antineoplásicos/administración & dosificación , Interferón-alfa/administración & dosificación , Linfoma Cutáneo de Células T/tratamiento farmacológico , Terapia PUVA , Neoplasias Cutáneas/tratamiento farmacológico , Adulto , Estudios de Seguimiento , Humanos , Inyecciones Intralesiones , Linfoma Cutáneo de Células T/diagnóstico , Linfoma Cutáneo de Células T/patología , Masculino , Inducción de Remisión , Piel/patología , Neoplasias Cutáneas/diagnóstico , Neoplasias Cutáneas/patología , Factores de Tiempo
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