Emerging molecular and environmental biomarkers of shrimp allergy in African Americans in the US.

IF 3.1 Q2 ALLERGY
Frontiers in allergy Pub Date : 2026-04-10 eCollection Date: 2026-01-01 DOI:10.3389/falgy.2026.1817101
Tanmoy Mondal, Dalyngs Duvelsaint, Kingston Griffin, McKenzie Williams, Oluwaseyitodun Johnson, Zara Campbell, Carla M Davis
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Abstract

Shrimp allergy (SA), a major cause of food-induced anaphylaxis, represents a disproportionate and under-characterized burden among African American (AA) populations in the United States. Unlike many childhood food allergies, SA is often persistent and commonly presents in adolescence or adulthood, suggesting a role for cumulative environmental exposures in disrupting oral tolerance. A key diagnostic challenge in AA communities is the high prevalence of IgE sensitization to shrimp tropomyosin (Pen a 1), which shares strong structural homology with cockroach and house dust mite tropomyosins, leading to frequent cross-reactive but clinically irrelevant sensitization in urban settings. This review critically examines molecular and environmental biomarkers of SA with a focus on AA populations. We assess the limitations of extract-based IgE testing and component-resolved diagnostics, highlighting how single-component assays may overestimate true clinical allergy. We emphasize the added value of functional assays, particularly the basophil activation test, in distinguishing sensitization from challenge-confirmed allergies. Mechanistically, we discuss how chronic exposure to indoor arthropod allergens, air pollution, and socioenvironmental stressors may drive epithelial barrier dysfunction, IL-33 release, and amplification of type 2 immune pathways, lowering reaction thresholds and influencing disease persistence. We identify key gaps, including limited oral food challenge-confirmed data and underrepresentation of AA cohorts. Finally, we propose equity-centered, integrative research frameworks combining molecular diagnostics, functional assays, environmental assessment, and multi-omics to improve diagnostic precision and advance clinical equity in SA care.

美国非裔美国人虾过敏的新兴分子和环境生物标志物。
虾过敏(SA)是食物过敏性反应的主要原因,在美国非裔美国人(AA)人群中表现出不成比例和特征不足的负担。与许多儿童食物过敏不同,SA通常是持续性的,通常出现在青春期或成年期,这表明累积的环境暴露在破坏口腔耐受方面的作用。在AA社区中,一个关键的诊断挑战是对虾原肌球蛋白的IgE致敏率很高(Pen A 1),虾原肌球蛋白与蟑螂和屋尘螨原肌球蛋白具有很强的结构同源性,导致城市环境中频繁的交叉反应但与临床无关的致敏。这篇综述对SA的分子和环境生物标志物进行了批判性的研究,重点是AA群体。我们评估了基于提取物的IgE检测和成分分解诊断的局限性,强调了单组分分析可能高估真实的临床过敏。我们强调功能分析的附加价值,特别是嗜碱性细胞激活试验,在区分致敏性和挑战确认的过敏。从机制上讲,我们讨论了长期暴露于室内节肢动物过敏原、空气污染和社会环境压力因素如何驱动上皮屏障功能障碍、IL-33释放和2型免疫途径的扩增,降低反应阈值并影响疾病的持久性。我们确定了关键的差距,包括有限的口腔食物挑战证实的数据和AA队列的代表性不足。最后,我们提出了以公平为中心的综合研究框架,结合分子诊断、功能分析、环境评估和多组学,以提高诊断精度和促进SA护理的临床公平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.80
自引率
0.00%
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0
审稿时长
12 weeks
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