Carnazza Michelle, Werner Robert, Tiwari Raj K, Geliebter Jan, Li Xiu-Min, Yang Nan
General Nutraceutical Technology, LLC, Elmsford, NY 10523, USA.
Department of Pathology, Microbiology & Immunology, New York Medical College, Valhalla, NY 10595, USA.
Int J Mol Sci. 2025 Feb 13;26(4):1563. doi: 10.3390/ijms26041563.
Immunoglobulin E (IgE)-mediated food allergy has been dramatically increasing in incidence over the last few decades. The combinations of both genetic and environmental factors that affect the microbiome and immune system have demonstrated significant roles in its pathogenesis. The morbidity, and at times mortality, that occurs as the result of this specific, reproducible, but impaired immune response is due to the nature of the shift from a regulatory T (Treg) cellular response to a T helper 2 (Th2) cellular response. This imbalance caused by food allergens results in an interleukin (IL)-4 and IL-13 dominant environment that drives B cell activation and differentiation into IgE-producing plasma cells. The resulting symptoms can range from mild to more severe anaphylaxis, and even death. Current therapeutic strategies involve avoidance and broad symptom management upon accidental exposure; however, no definitive cure exists. This narrative review highlights how the elucidation of the pathogenesis of IgE-mediated food allergy resulted in the development of therapeutics that are more specific to these individual receptors and molecules which have been relatively successful in mitigating this potentially life-threatening allergic response. However, potential adverse effects and re-sensitization following the conclusion of treatment has urged the need for improved therapeutic methods. Therefore, given the understanding of their mechanism of action and the overlap with the mechanism of IgE-mediated food allergies, probiotics and small molecule natural compounds may provide novel therapeutic and preventative strategies. This is compelling, as they have demonstrated success in clinical trials and may provide hope to improve quality of life in allergy patients.
在过去几十年中,免疫球蛋白E(IgE)介导的食物过敏发病率急剧上升。影响微生物群和免疫系统的遗传和环境因素的综合作用已在其发病机制中显示出重要作用。这种特定的、可重复但受损的免疫反应所导致的发病率,有时甚至是死亡率,是由于从调节性T(Treg)细胞反应向辅助性T2(Th2)细胞反应转变的性质所致。食物过敏原引起的这种失衡导致白细胞介素(IL)-4和IL-13占主导的环境,驱动B细胞活化并分化为产生IgE的浆细胞。由此产生的症状范围从轻度到更严重的过敏反应,甚至死亡。目前的治疗策略包括避免接触以及在意外接触后进行广泛的症状管理;然而,尚无确切的治愈方法。这篇叙述性综述强调了对IgE介导食物过敏发病机制的确切了解如何促成了更针对这些特定受体和分子的治疗方法的开发,这些方法在减轻这种潜在的危及生命的过敏反应方面相对成功。然而,治疗结束后的潜在不良反应和重新致敏促使人们需要改进治疗方法。因此,鉴于对益生菌和小分子天然化合物作用机制的了解以及它们与IgE介导食物过敏机制的重叠,它们可能提供新的治疗和预防策略。这很有吸引力,因为它们在临床试验中已显示出成效,可能为改善过敏患者的生活质量带来希望。