Cooper Philip J
Laboratorio de Investigaciones, Hospital Pedro Vicente Maldonado, Pichincha Province, Ecuador.
Clin Rev Allergy Immunol. 2004 Feb;26(1):5-14. doi: 10.1385/CRIAI:26:1:5.
Microbial exposures in early life may provide important signals for immune maturation and the development of an antiinflammatory network thereby preventing the development of dysregulated immune responses such as that associated with allergic disease. The human immune system has evolved in the presence of intense helminth infections and has developed regulatory mechanisms to limit the harmful inflammation that can be caused by the potent allergens secreted by these chronic pathogens. Geohelminth infections are highly prevalent childhood infections, and there is strong evidence that chronic geohelminth infections provide protection against atopy in the rural tropics. Because the early environmental exposures that may lead to the development of atopy are likely to occur in the first few years of life, geohelminth infections may exert their protective effects at this time. Early exposures to geohelminth antigens could occur transplacentally, through breast milk, or through early infant exposures, and could induce tolerance to parasite antigens resulting in suppressed allergic responses to the parasite. Tolerization to parasite antigens could suppress allergic responses to inhalant allergens through bystander effects or through tolerization of crossreactive epitopes that are shared between geohelminth parasites and inhalant allergens. Tolerization to crossreactive allergens could occur by thymic deletion or through peripheral mechanisms such as regulatory T cells. Immunologic studies of the mechanisms by which early exposures to geohelminth infections affect immune polarization to inhalant allergens are likely to provide important insights into the early regulation of the immune response and may lead to the design of novel interventions for the prevention of allergic disease.
生命早期的微生物暴露可能为免疫成熟和抗炎网络的发展提供重要信号,从而预防失调的免疫反应的发生,如与过敏性疾病相关的免疫反应。人类免疫系统在严重的蠕虫感染环境中进化,并发展出调节机制来限制这些慢性病原体分泌的强效过敏原可能引起的有害炎症。土源性蠕虫感染是儿童期高度流行的感染,有强有力的证据表明,慢性土源性蠕虫感染可预防热带农村地区的特应性疾病。由于可能导致特应性疾病发生的早期环境暴露很可能发生在生命的最初几年,土源性蠕虫感染可能在这个时期发挥其保护作用。早期接触土源性蠕虫抗原可能通过胎盘、母乳或婴儿早期接触发生,并可诱导对寄生虫抗原的耐受,从而抑制对寄生虫的过敏反应。对寄生虫抗原的耐受可通过旁观者效应或通过对土源性蠕虫寄生虫和吸入性过敏原共有的交叉反应表位的耐受来抑制对吸入性过敏原的过敏反应。对交叉反应性过敏原的耐受可通过胸腺缺失或通过外周机制如调节性T细胞发生。对早期接触土源性蠕虫感染影响对吸入性过敏原的免疫极化的机制进行免疫学研究,可能会为免疫反应的早期调节提供重要见解,并可能导致设计预防过敏性疾病的新型干预措施。