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排泄/分泌产物:一个尚未开发的针对食物过敏的耐受性免疫治疗药物库。

excretory/secretory products: an untapped library of tolerogenic immunotherapeutics against food allergy.

作者信息

Rogers Madeleine, Kamath Sandip, McManus Donald, Jones Malcolm, Gordon Catherine, Navarro Severine

机构信息

Faculty of Medicine University of Queensland Brisbane QLD Australia.

QIMR Berghofer Medical Research Institute Brisbane QLD Australia.

出版信息

Clin Transl Immunology. 2024 Aug 29;13(9):e70001. doi: 10.1002/cti2.70001. eCollection 2024 Sep.

Abstract

Food allergy (FA) is considered the 'second wave' of the allergy epidemic in developed countries after asthma and allergic rhinitis with a steadily growing burden of 40%. The absence of early childhood pathogen stimulation embodied by the hygiene hypothesis is one explanation, and in particular, the eradication of parasitic helminths could be at play. Infections with parasites spp. have been found to have a negative correlation with allergic diseases. Schistosomes induce regulatory responses to evade immune detection and ensure their long-term survival. This is achieved via excretory/secretory (E/S) products, consisting of proteins, lipids, metabolites, nucleic acids and extracellular vesicles, representing an untapped therapeutic avenue for the treatment of FA without the unpleasant side-effects and risks associated with live infection. Schistosome-derived immunotherapeutic development is in its infancy and novel discoveries are heavily technology dependent; thus, it is essential to better understand how newly identified molecules interact with host immune systems to ensure safety and successful translation. This review will outline the identified -derived E/S products at all life cycle stages and discuss known mechanisms of action and their ability to suppress FA.

摘要

食物过敏(FA)被认为是发达国家继哮喘和过敏性鼻炎之后过敏流行的“第二波浪潮”,其负担正以40%的速度稳步增长。卫生假说所体现的幼儿期病原体刺激的缺失是一种解释,特别是寄生虫的根除可能起到了作用。已发现感染寄生虫与过敏性疾病呈负相关。血吸虫诱导调节性反应以逃避免疫检测并确保其长期存活。这是通过排泄/分泌(E/S)产物实现的,这些产物由蛋白质、脂质、代谢物、核酸和细胞外囊泡组成,代表了一种未开发的治疗FA的途径,且没有与活感染相关的不良副作用和风险。血吸虫衍生的免疫疗法尚处于起步阶段,新发现严重依赖技术;因此,更好地了解新鉴定的分子如何与宿主免疫系统相互作用以确保安全性和成功转化至关重要。本综述将概述在血吸虫所有生命周期阶段鉴定出的E/S产物,并讨论已知的作用机制及其抑制FA的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/297b/11359118/02c71035ba7e/CTI2-13-e70001-g006.jpg

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