Müller H, End C, Weiss C, Renner M, Bhandiwad A, Helmke B M, Gassler N, Hafner M, Poustka A, Mollenhauer J, Poeschl J
Division of Neonatology, Department of Pediatrics, University of Heidelberg, Heidelberg, Germany.
Clin Exp Immunol. 2008 Jan;151(1):123-9. doi: 10.1111/j.1365-2249.2007.03528.x. Epub 2007 Nov 7.
Deleted in Malignant Brain Tumours 1 (DMBT1) is a secreted scavenger receptor cysteine-rich protein that binds and aggregates various bacteria and viruses in vitro. Studies in adults have shown that DMBT1 is expressed mainly by mucosal epithelia and glands, in particular within the respiratory tract, and plays a role in innate immune defence. We hypothesized that respiratory DMBT1 levels may be influenced by various developmental and clinical factors such as maturity, age and bacterial infection. DMBT1 levels were studied in 205 tracheal aspirate samples of 82 ventilated preterm and full-term infants by enzyme-linked immunosorbent assay. Possible effects of various clinical parameters were tested by multiple regression analysis. DMBT1 levels increased significantly with lung maturity (P < 0.0001 for both gestational and postnatal age) and in small-for-gestational-age infants (P = 0.0179). An increase of respiratory DMBT1 levels was detected in neonatal infections (P < 0.0001). These results were supported by Western blotting. Immunohistochemical analyses of archived newborn lung sections (n = 17) demonstrated high concentrations of DMBT1 in lungs of neonates with bacterial infections. Our data show that preterm infants are able to up-regulate DMBT1 in infection as an unspecific immune reaction.
恶性脑肿瘤缺失基因1(DMBT1)是一种分泌型富含半胱氨酸的清道夫受体蛋白,在体外可结合并聚集多种细菌和病毒。针对成年人的研究表明,DMBT1主要由黏膜上皮和腺体表达,尤其是在呼吸道内,并且在先天性免疫防御中发挥作用。我们推测,呼吸道DMBT1水平可能受多种发育和临床因素影响,如成熟度、年龄和细菌感染。通过酶联免疫吸附测定法,对82例接受机械通气的早产儿和足月儿的205份气管吸出物样本中的DMBT1水平进行了研究。通过多元回归分析测试了各种临床参数的可能影响。DMBT1水平随肺成熟度显著升高(胎龄和出生后年龄的P值均<0.0001),并且在小于胎龄儿中也升高(P = 0.0179)。在新生儿感染中检测到呼吸道DMBT1水平升高(P < 0.0001)。蛋白质印迹法支持了这些结果。对存档的新生儿肺组织切片(n = 17)进行的免疫组织化学分析表明,细菌感染新生儿的肺中DMBT1浓度较高。我们的数据表明,早产儿在感染时能够上调DMBT1作为一种非特异性免疫反应。