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J Immunol ; 208(2): 267-277, 2022 01 15.
Artículo en Inglés | MEDLINE | ID: mdl-35017216

RESUMEN

Alpha-gal syndrome (AGS) describes a collection of symptoms associated with IgE-mediated hypersensitivity responses to the glycan galactose-alpha-1,3-galactose (alpha-gal). Individuals with AGS develop delayed hypersensitivity reactions, with symptoms occurring >2 h after consuming mammalian ("red") meat and other mammal-derived food products. The mechanisms of pathogenesis driving this paradigm-breaking food allergy are not fully understood. We review the role of tick bites in the development of alpha-gal-specific IgE and highlight innate and adaptive immune cells possibly involved in alpha-gal sensitization. We discuss the impact of alpha-gal glycosylation on digestion and metabolism of alpha-gal glycolipids and glycoproteins, and the implications for basophil and mast cell activation and mediator release that generate allergic symptoms in AGS.


Asunto(s)
Hipersensibilidad a los Alimentos/inmunología , Hipersensibilidad a los Alimentos/fisiopatología , Inmunoglobulina E/inmunología , Mordeduras de Garrapatas/fisiopatología , Animales , Bacterias/inmunología , Modelos Animales de Enfermedad , Glucolípidos/metabolismo , Glicoproteínas/metabolismo , Humanos , Hipersensibilidad Inmediata/inmunología , Hipersensibilidad Inmediata/patología , Linfocitos/inmunología , Ratones , Carne Roja/efectos adversos , Mordeduras de Garrapatas/microbiología
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