Michelet Marine, Schluckebier Dominique, Petit Laetitia-Marie, Caubet Jean-Christoph
Children Hospital, Pediatric Allergology Unit CHU Toulouse, Toulouse, France.
Geneva University Hospitals, Pediatric Gastroenterology Unit.
J Asthma Allergy. 2017 Jun 27;10:197-207. doi: 10.2147/JAA.S100379. eCollection 2017.
Food protein-induced enterocolitis syndrome (FPIES) is a potentially severe presentation of non-IgE-mediated gastrointestinal food allergy (non-IgE-GI-FA) with heterogeneous clinical manifestations. Acute FPIES is typically characterized by profuse vomiting and lethargy, occurring classically 1-4 hours after ingestion of the offending food. When continuously exposed to the incriminated food, a chronic form has been described with persistent vomiting, diarrhea, and/or failure to thrive. Although affecting mainly infants, FPIES has also been described in adults. Although FPIES is actually one of the most actively studied non-IgE-GI-FAs, epidemiologic data are lacking, and estimation of the prevalence is based on a limited number of prospective studies. The exact pathomechanisms of FPIES remain not well defined, but recent data suggest involvement of neutrophils and mast cells, in addition to T cells. There is a wide range of food allergens that can cause FPIES with some geographical variations. The most frequently incriminated foods are cow milk, soy, and grains in Europe and USA. Furthermore, FPIES can be induced by foods usually considered as hypoallergenic, such as chicken, potatoes or rice. The diagnosis relies currently on typical clinical manifestations, resolving after the elimination of the offending food from the infant's/child's diet and/or an oral food challenge (OFC). The prognosis is usually favorable, with the vast majority of the case resolving before 5 years of age. Usually, assessment of tolerance acquisition by OFC is proposed every 12-18 months. Of note, a switch to an IgE-mediated FA is possible and has been suggested to be associated with a more severe phenotype. Avoiding the offending food requires education of the family of the affected child. A multidisciplinary approach including ideally allergists, gastroenterologists, dieticians, specialized nurses, and caregivers is often useful to optimize the management of these patients, that might be difficult.
食物蛋白诱导的小肠结肠炎综合征(FPIES)是一种非IgE介导的胃肠道食物过敏(non-IgE-GI-FA)的潜在严重表现形式,临床表现具有异质性。急性FPIES的典型特征是大量呕吐和嗜睡,通常在摄入致病食物后1 - 4小时出现。当持续接触可疑食物时,会出现慢性形式,表现为持续性呕吐、腹泻和/或生长发育迟缓。虽然FPIES主要影响婴儿,但在成人中也有报道。尽管FPIES实际上是研究最活跃的非IgE-GI-FA之一,但缺乏流行病学数据,患病率估计基于有限数量的前瞻性研究。FPIES的确切发病机制仍未明确,但最近的数据表明,除了T细胞外,中性粒细胞和肥大细胞也参与其中。有多种食物过敏原可导致FPIES,存在一些地理差异。在欧洲和美国,最常被认为是致病的食物是牛奶、大豆和谷物。此外,FPIES可由通常被认为是低过敏性的食物诱发,如鸡肉、土豆或大米。目前,诊断依赖于典型的临床表现,在从婴儿/儿童饮食中去除致病食物和/或进行口服食物激发试验(OFC)后症状缓解。预后通常良好,绝大多数病例在5岁前痊愈。通常建议每12 - 18个月通过OFC评估耐受性的获得情况。值得注意的是,有可能转变为IgE介导的食物过敏,并且有人认为这与更严重的表型有关。避免食用致病食物需要对受影响儿童的家庭进行教育。多学科方法,理想情况下包括过敏症专科医生、胃肠病学家、营养师、专科护士和护理人员,通常有助于优化这些可能难以管理的患者的治疗。