Mansbach Jonathan M, Hasegawa Kohei, Ajami Nadim J, Petrosino Joseph F, Piedra Pedro A, Tierney Courtney N, Espinola Janice A, Camargo Carlos A
Department of Medicine, Boston Children's Hospital.
Department of Emergency Medicine, Massachusetts General Hospital, Harvard Medical School, Boston.
Clin Infect Dis. 2017 Sep 15;65(6):967-975. doi: 10.1093/cid/cix483.
LL-37 is a host defense peptide with antimicrobial and immunomodulatory properties. We examined the relation of serum LL-37 levels to the severity of bronchiolitis and viral etiology.
We performed a 17-center prospective cohort study in infants hospitalized with bronchiolitis over 3 winters (2011-2014). Site teams collected clinical data, nasopharyngeal aspirates and serum. We used real-time polymerase chain reaction to test nasopharyngeal aspirates for 16 viruses. We tested serum for LL-37. Severity of bronchiolitis was defined by intensive care use and hospital length of stay. Viral etiology was defined as respiratory syncytial virus (RSV) or rhinovirus (RV), including coinfections with other viruses.
The median age of the 1005 enrolled infants was 3 months (interquartile range, 2-6 months). After adjustment for 12 variables, LL-37 levels in the lowest quartile, compared with the highest, were associated both with intensive care use (adjusted odds ratio [aOR], 1.97; P = .01) and longer hospital stay (1.34; P < .001). In separate multivariable models, infants with LL-37 levels in the lowest 3 quartiles, compared with the highest, were more likely to have RSV (eg, aOR, 2.6 [lowest quartile]; P < .001 [all quartiles]). By contrast, infants with the lowest 3 LL-37 quartiles were less likely to have RV (eg, aOR, 0.5 [lowest quartile]; Pall quartiles ≤ .03 [all quartiles]).
In a large multicenter study of infants hospitalized with bronchiolitis, lower levels of serum LL-37 were associated with increased severity of illness. There was also an inverse relationship between LL-37 levels and the most common virus causing bronchiolitis, RSV. These findings highlight the role of LL-37 in the pathogenesis of bronchiolitis.
LL-37是一种具有抗菌和免疫调节特性的宿主防御肽。我们研究了血清LL-37水平与细支气管炎严重程度及病毒病因之间的关系。
我们在3个冬季(2011 - 2014年)对因细支气管炎住院的婴儿进行了一项17中心的前瞻性队列研究。各研究点团队收集临床数据、鼻咽抽吸物和血清。我们使用实时聚合酶链反应检测鼻咽抽吸物中的16种病毒。检测血清中的LL-37。细支气管炎的严重程度通过重症监护的使用情况和住院时间来定义。病毒病因定义为呼吸道合胞病毒(RSV)或鼻病毒(RV),包括与其他病毒的混合感染。
1005名入组婴儿的中位年龄为3个月(四分位间距,2 - 6个月)。在对12个变量进行调整后,与最高四分位相比,最低四分位的LL-37水平与重症监护的使用(调整后的优势比[aOR],1.97;P = 0.01)以及更长的住院时间(1.34;P < 0.001)均相关。在单独的多变量模型中,与最高四分位相比,LL-37水平处于最低3个四分位的婴儿更有可能感染RSV(例如,最低四分位的aOR为2.6;所有四分位的P < 0.001)。相比之下,LL-37处于最低3个四分位的婴儿感染RV的可能性较小(例如,最低四分位的aOR为0.5;所有四分位的P ≤ 0.03)。
在一项对因细支气管炎住院婴儿的大型多中心研究中,血清LL-37水平较低与疾病严重程度增加相关。LL-37水平与引起细支气管炎最常见的病毒RSV之间也存在负相关关系。这些发现突出了LL-37在细支气管炎发病机制中的作用。