Saglani Sejal, Malmström Kristiina, Pelkonen Anna S, Malmberg L Pekka, Lindahl Harry, Kajosaari Merja, Turpeinen Markku, Rogers Andrew V, Payne Donald N, Bush Andrew, Haahtela Tari, Mäkelä Mika J, Jeffery Peter K
Lung Pathology, Royal Brompton Hospital, Sydney Street, London SW3 6NP, UK.
Am J Respir Crit Care Med. 2005 Apr 1;171(7):722-7. doi: 10.1164/rccm.200410-1404OC. Epub 2005 Jan 18.
We hypothesized that the epithelial reticular basement membrane (RBM) thickening and eosinophilic inflammation characteristic of asthma would be present in symptomatic infants with reversible airflow obstruction.
RBM thickness and numbers of inflammatory cells were determined in ultrathin sections of endobronchial biopsies obtained from 53 infants during clinical bronchoscopy for severe wheeze and/or cough. Group A: 16 infants with a median age of 12 months (range 3.4-26 months), with decreased specific airway conductance (sGaw) and bronchodilator reversibility; Group B: 22 infants with a median age of 12.4 months (5.1-25.9 months), with decreased sGaw but without bronchodilator reversibility; and Group C: 15 infants with a median age of 11.5 months (3.4-24.3 months) with normal sGaw. Additional comparisons were made with the following groups. Group D: 17 children, median age 10.3 years (6-16 years), with difficult asthma; Group E: 10 pediatric control subjects without asthma, median age 10 years (6-16 years); and Group F: nine adult normal, healthy control subjects, median age 27 years (21-42 years).
There were no significant differences in RBM thickness or inflammatory cell number between the infant groups. RBM thickness was similar in the infants and Groups E and F. However, the RBM in all infant groups (Group A: median 4.3 microm [range 2.8-9.2 microm]; Group B: median 4.15 microm [range 2.7-5.8 microm]; Group C: median 3.8 microm [range 2.7-5.5 microm]) was significantly less thick than that in the older children with asthma (Group D: median 8.3 microm [range 5.3-12.7 microm]; p < 0.001).
RBM thickening and the eosinophilic inflammation characteristic of asthma in older children and adults are not present in symptomatic infants with reversible airflow obstruction, even in the presence of atopy.
我们假设哮喘所特有的上皮网状基底膜(RBM)增厚和嗜酸性粒细胞炎症会出现在有可逆性气流阻塞的有症状婴儿中。
在53例因严重喘息和/或咳嗽而接受临床支气管镜检查的婴儿的支气管活检超薄切片中测定RBM厚度和炎症细胞数量。A组:16例婴儿,中位年龄12个月(范围3.4 - 26个月),特异性气道传导率(sGaw)降低且支气管扩张剂可逆性降低;B组:22例婴儿,中位年龄12.4个月(5.1 - 25.9个月),sGaw降低但无支气管扩张剂可逆性;C组:15例婴儿,中位年龄11.5个月(3.4 - 24.3个月),sGaw正常。还与以下几组进行了额外比较。D组:17名儿童,中位年龄10.3岁(6 - 16岁),患有难治性哮喘;E组:10名无哮喘的儿科对照受试者,中位年龄10岁(6 - 16岁);F组:9名正常健康的成人对照受试者,中位年龄27岁(21 - 42岁)。
婴儿组之间的RBM厚度或炎症细胞数量无显著差异。婴儿组与E组和F组的RBM厚度相似。然而,所有婴儿组(A组:中位4.3微米[范围2.8 - 9.2微米];B组:中位4.15微米[范围2.7 - 5.8微米];C组:中位3.8微米[范围2,7 - 5.5微米])的RBM明显比患有哮喘的大龄儿童(D组:中位8.3微米[范围5.3 - 12.7微米];p < 0.001)薄。
即使存在特应性,有可逆性气流阻塞的有症状婴儿中不存在大龄儿童和成人哮喘所特有的RBM增厚和嗜酸性粒细胞炎症。