Département Médicaments et Technologies pour la Santé (DMTS), Université Paris-Saclay, CEA, INRAe, Service de Pharmacologie et d'Immunoanalyse, 91190 Gif-sur-Yvette, France.
INRAe, UR1268 Biopolymères, Intéractions et Assemblages (BIA), 44316 Nantes, France.
Nutrients. 2022 Feb 14;14(4):790. doi: 10.3390/nu14040790.
Symptom occurrence at the first ingestion suggests that food allergy may result from earlier sensitization via non-oral routes. We aimed to characterize the cellular populations recruited at various mucosal and immune sites after experimental sensitization though different routes. BALB/cJ mice were exposed to a major allergenic food (peanut) mixed with cholera toxin via the intra-gastric (i.g.), respiratory, cutaneous, or intra-peritoneal (i.p.) route. We assessed sensitization and elicitation of the allergic reaction and frequencies of T cells, innate lymphoid cells (ILC), and inflammatory and dendritic cells (DC) in broncho-alveolar lavages (BAL), lungs, skin, intestine, and various lymph nodes. All cellular data were analyzed through non-supervised and supervised uni/multivariate analysis. All exposure routes, except cutaneous, induced sensitization, but intestinal allergy was induced only in i.g.- and i.p.-exposed mice. Multivariate analysis of all cellular constituents did not discriminate i.g. from control mice. Conversely, respiratory-sensitized mice constituted a distinct cluster, characterized by high local inflammation and immune cells recruitment. Those mice also evidenced changes in ILC frequencies at distant site (intestine). Despite absence of sensitization, cutaneous-exposed mice evidenced comparable changes, albeit less intense. Our study highlights that the initial route of sensitization to a food allergen influences the nature of the immune responses at various mucosal sites. Interconnections of mucosal immune systems may participate in the complexity of clinical manifestations as well as in the atopic march.
症状首次出现提示食物过敏可能是由非口服途径的早期致敏引起的。我们旨在通过不同途径描述实验致敏后各种粘膜和免疫部位募集的细胞群体。将 BALB/cJ 小鼠通过胃内(i.g.)、呼吸、皮肤或腹腔(i.p.)途径暴露于主要过敏原食物(花生)与霍乱毒素混合。我们评估了过敏反应的致敏和激发以及支气管肺泡灌洗液(BAL)、肺、皮肤、肠道和各种淋巴结中的 T 细胞、先天淋巴细胞(ILC)、炎症和树突状细胞(DC)的频率。所有细胞数据均通过非监督和监督的单变量/多变量分析进行分析。除了皮肤,所有暴露途径都诱导了致敏,但仅在 i.g.和 i.p.暴露的小鼠中诱导了肠道过敏。所有细胞成分的多元分析未能将 i.g.与对照小鼠区分开来。相反,呼吸致敏的小鼠构成了一个独特的簇,其特征是局部炎症和免疫细胞募集增加。这些小鼠还在远处部位(肠道)的 ILC 频率上发生了变化。尽管没有致敏,但皮肤暴露的小鼠也出现了类似的变化,尽管强度较低。我们的研究强调,食物过敏原的初始致敏途径会影响各种粘膜部位的免疫反应性质。粘膜免疫系统的相互联系可能参与了临床表现的复杂性以及特应性进展。