Department of Microbiology and Immunology, Cornell University, Ithaca, NY, 14853, USA.
World J Pediatr. 2010 May;6(2):111-8. doi: 10.1007/s12519-010-0026-1. Epub 2010 May 21.
Childhood susceptibility to diseases linked with immune dysfunction affects over a quarter of the pediatric population in some countries. While this alone is a significant health issue, the actual impact of immune-related diseases extends over a lifetime and involves additional secondary conditions. Some comorbidities are well known (e.g., allergic rhinitis and asthma). However, no systematic approach has been used to identify life-long patterns of immune-based disease where the primary condition arises in childhood. Such information is useful for both disease prevention and treatment approaches.
Recent primary research papers as well as review articles were obtained from PubMed, Chem Abstracts, Biosis and from the personal files of the authors. Search words used were: the diseases and conditions shown Figs. 1 and 2 in conjunction with comorbid, comorbidities, pediatric, childhood, adult, immune, immune dysfunction, allergy, autoimmune, inflammatory, infectious, health risks, environment, risk factors.
Childhood diseases such as asthma, type-1 diabetes, inflammatory bowel disease, respiratory infections /rhinitis, recurrent otitis media, pediatric celiac, juvenile arthritis and Kawasaki disease are examples of significant childhood health problems where immune dysfunction plays a significant role. Each of these pediatric diseases is associated with increased risk of several secondary conditions, many of which appear only later in life. To illustrate, four prototypes of immune-related disease patterns (i.e., allergy, autoimmunity, inflammation and infectious disease) are shown as tools for: 1) enhanced disease prevention; 2) improved management of immune-based pediatric diseases; and 3) better recognition of underlying pediatric immune dysfunction.
Identification of immune-related disease patterns beginning in childhood provides the framework for examining the underlying immune dysfunctions that can contribute to additional diseases in later life. Many pediatric diseases associated with dysfunctional immune responses have been linked with an elevated risk of other diseases or conditions as the child ages. Diseases within a pattern may be interlinked based on underlying immune dysfunctions and/or current therapeutic approaches for managing the entryway diseases. It may be beneficial to consider treatment options for the earliest presenting diseases that will concomitantly reduce the risk of immune-linked secondary conditions. Additionally, improved disease prevention is possible with more relevant and age-specific immune safety testing.
儿童易患与免疫功能障碍相关的疾病,在一些国家影响了超过四分之一的儿科人群。虽然这本身就是一个重大的健康问题,但免疫相关疾病的实际影响会持续一生,并涉及到其他继发性疾病。一些合并症是众所周知的(例如过敏性鼻炎和哮喘)。然而,目前还没有系统的方法来确定儿童期出现原发性疾病的终生免疫性疾病模式。这些信息对于疾病预防和治疗方法都很有用。
最近的主要研究论文和综述文章均来自 PubMed、Chem Abstracts、Biosis 和作者的个人文件。使用的搜索词是:图 1 和图 2 所示的疾病和病症,以及合并症、合并症、儿科、儿童、成人、免疫、免疫功能障碍、过敏、自身免疫、炎症、感染、健康风险、环境、危险因素。
哮喘、1 型糖尿病、炎症性肠病、呼吸道感染/鼻炎、复发性中耳炎、小儿乳糜泻、青少年关节炎和川崎病等儿童疾病就是免疫功能障碍起重要作用的重大儿童健康问题的例子。这些儿科疾病中的每一种都与多种继发性疾病的风险增加有关,其中许多疾病仅在以后的生活中出现。例如,免疫相关疾病模式的四种原型(即过敏、自身免疫、炎症和传染病)可用作以下工具:1)增强疾病预防;2)改善免疫性儿科疾病的管理;3)更好地认识潜在的儿科免疫功能障碍。
从儿童期开始识别与免疫相关的疾病模式为研究导致以后生活中其他疾病的潜在免疫功能障碍提供了框架。许多与免疫反应功能障碍相关的儿科疾病与随着儿童年龄增长而患其他疾病或病症的风险增加有关。模式内的疾病可能基于潜在的免疫功能障碍和/或管理入门疾病的当前治疗方法而相互关联。考虑对最早出现的疾病进行治疗选择可能会同时降低免疫相关继发性疾病的风险,这可能是有益的。此外,通过更相关和特定于年龄的免疫安全性测试,还可以更好地进行疾病预防。