Serum LL-37 Levels Associated With Severity of Bronchiolitis and Viral Etiology

被引:28
作者
Mansbach, Jonathan M. [1 ]
Hasegawa, Kohei [2 ]
Ajami, Nadim J. [3 ]
Petrosino, Joseph F. [3 ]
Piedra, Pedro A. [4 ]
Tierney, Courtney N. [2 ]
Espinola, Janice A. [2 ]
Camargo, Carlos A. [2 ]
机构
[1] Boston Childrens Hosp, Dept Med, Boston, MA 02115 USA
[2] Harvard Med Sch, Massachusetts Gen Hosp, Dept Emergency Med, Boston, MA USA
[3] Alkek Ctr Metagen & Microbiome Res, Dept Mol Virol & Microbiol, Houston, TX USA
[4] Baylor Coll Med, Dept Mol Virol & Microbiol & Pediat, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
bronchiolitis; LL-37; respiratory syncytial virus; microbiota; severity of illness; RESPIRATORY SYNCYTIAL VIRUS; LENGTH-OF-STAY; REAL-TIME PCR; VITAMIN-D; PROSPECTIVE MULTICENTER; ANTIMICROBIAL PEPTIDES; UNITED-STATES; NASOPHARYNGEAL MICROBIOTA; HUMAN CATHELICIDIN; CONTROLLED-TRIAL;
D O I
10.1093/cid/cix483
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. 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. Methods. We performed a 17-center prospective cohort study in infants hospitalized with bronchiolitis over 3 winters (20112014). 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. Results. 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]; P (all quartiles) <= .03 [all quartiles]). Conclusions. 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.
引用
收藏
页码:967 / 975
页数:9
相关论文
共 38 条
[1]   Mechanisms and consequences of bacterial resistance to antimicrobial peptides [J].
Andersson, D. I. ;
Hughes, D. ;
Kubicek-Sutherland, J. Z. .
DRUG RESISTANCE UPDATES, 2016, 26 :43-57
[2]   Respiratory viral infections in patients with chronic, obstructive pulmonary disease [J].
Beckham, JD ;
Cadena, A ;
Lin, JJ ;
Piedra, PA ;
Glezen, WP ;
Greenberg, SB ;
Atmar, RL .
JOURNAL OF INFECTION, 2005, 50 (04) :322-330
[3]   Cathelicidins Have Direct Antiviral Activity against Respiratory Syncytial Virus In Vitro and Protective Function In Vivo in Mice and Humans [J].
Currie, Silke M. ;
Findlay, Emily Gwyer ;
McFarlane, Amanda J. ;
Fitch, Paul M. ;
Boettcher, Bettina ;
Colegrave, Nick ;
Paras, Allan ;
Jozwik, Agnieszka ;
Chiu, Christopher ;
Schwarze, Juergen ;
Davidson, Donald J. .
JOURNAL OF IMMUNOLOGY, 2016, 196 (06) :2699-2710
[4]   The Human Cathelicidin LL-37 Has Antiviral Activity against Respiratory Syncytial Virus [J].
Currie, Silke M. ;
Findlay, Emily Gwyer ;
McHugh, Brian J. ;
Mackellar, Annie ;
Man, Tian ;
Macmillan, Derek ;
Wang, Hongwei ;
Fitch, Paul M. ;
Schwarze, Juergen ;
Davidson, Donald J. .
PLOS ONE, 2013, 8 (08)
[5]   LL-37, the only human member of the cathelicidin family of antimicrobial peptides [J].
Durr, Ulrich H. N. ;
Sudheendra, U. S. ;
Ramamoorthy, Ayyalusamy .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2006, 1758 (09) :1408-1425
[6]   Low Plasma Level of Cathelicidin Antimicrobial Peptide (hCAP18) Predicts Increased Infectious Disease Mortality in Patients Undergoing Hemodialysis [J].
Gombart, Adrian F. ;
Bhan, Ishir ;
Borregaard, Niels ;
Tamez, Hector ;
Camargo, Carlos A. ;
Koeffler, H. Phillip ;
Thadhani, Ravi .
CLINICAL INFECTIOUS DISEASES, 2009, 48 (04) :418-424
[7]   Human cathelicidin antimicrobial peptide (CAMP) gene is a direct target of the vitamin D receptor and is strongly up-regulated in myeloid cells by 1,25-dihydroxyvitamin D3 [J].
Gombart, AF ;
Borregaard, N ;
Koeffler, HP .
FASEB JOURNAL, 2005, 19 (09) :1067-1077
[8]   High dose vitamin D administration in ventilated intensive care unit patients: A pilot double blind randomized controlled trial [J].
Han, Jenny E. ;
Jones, Jennifer L. ;
Tangpricha, Vin ;
Brown, Mona A. ;
Hao, Li ;
Hebbar, Gautam ;
Lee, Moon Jeong ;
Liu, Shuling ;
Brown, Lou Ann S. ;
Ziegler, Thomas R. ;
Martin, Greg S. .
JOURNAL OF CLINICAL AND TRANSLATIONAL ENDOCRINOLOGY, 2016, 4 :59-65
[9]   Human cathelicidin, LL-37, inhibits respiratory syncytial virus infection in polarized airway epithelial cells [J].
Harcourt J.L. ;
McDonald M. ;
Svoboda P. ;
Pohl J. ;
Tatti K. ;
Haynes L.M. .
BMC Research Notes, 9 (1)
[10]   Serumcathelicidin, nasopharyngeal microbiota, and disease severity among infants hospitalized with bronchiolitis [J].
Hasegawa, Kohei ;
Mansbach, Jonathan M. ;
Ajami, Nadim J. ;
Petrosino, Joseph F. ;
Freishtat, Robert J. ;
Teach, Stephen J. ;
Piedra, Pedro A. ;
Camargo, Carlos A., Jr. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2017, 139 (04) :1383-1386