| Literature DB >> 35017216 |
Audrey S Carson1, Aliyah Gardner1, Onyinye I Iweala2.
Abstract
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.Entities:
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Year: 2022 PMID: 35017216 PMCID: PMC8928418 DOI: 10.4049/jimmunol.2100712
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422