New Insights Into the Pathogenesis and Treatment of Necrotizing Enterocolitis: Toll-Like Receptors and Beyond

被引:112
作者
Afrazi, Amin
Sodhi, Chhinder P.
Richardson, Ward
Neal, Matthew
Good, Misty [2 ]
Siggers, Richard
Hackam, David J. [1 ]
机构
[1] Univ Pittsburgh, Childrens Hosp Pittsburgh, UPMC, Sch Med,Dept Surg, Pittsburgh, PA 15224 USA
[2] Univ Pittsburgh, Childrens Hosp Pittsburgh, Sch Med, Dept Pediat, Pittsburgh, PA 15224 USA
基金
美国国家卫生研究院;
关键词
PLATELET-ACTIVATING-FACTOR; BIRTH-WEIGHT INFANTS; NEONATAL-RAT MODEL; EPITHELIAL RESTITUTION; ENTEROCYTE MIGRATION; ADAPTIVE IMMUNITY; GENE-EXPRESSION; TLR4; LIPOPOLYSACCHARIDE; ENDOTOXIN;
D O I
10.1203/PDR.0b013e3182093280
中图分类号
R72 [儿科学];
学科分类号
100202 [儿科学];
摘要
Neerotizing enterocolitis (NEC) is the leading cause of death from gastrointestinal disease in the preterm infant. The dismal results of current treatment for NEC highlight the urgent need for greater understanding of the pathogenesis of this disease, and the importance of discovering novel, molecular-specific therapies for it. Current dogma indicates that NEC development reflects an abnormal response by the premature infant to the microbial flora that colonizes the gastrointestinal tract, although the mechanisms that mediate these abnormal bacterial-enterocyte interactions and the reasons for the particularly increased susceptibility of the premature infant to the development of NEC remain incompletely explained. Recent evidence has shed light on an emerging role for the Toll-like receptors (TLRs) of the innate immune system as central players in the pathways that signal in response to enteric bacteria resulting in the development of NEC. We now review recent advances in the field of NEC and identify several exciting potential avenues for novel treatments by focusing on abnormal TLR4 signaling in the premature intestine in the pathogenesis of NEC. In so doing, we seek to offer new hope to the patients and their families who are affected by this devastating disorder. (Pediatr Res 69: 183-188, 2011)
引用
收藏
页码:183 / 188
页数:6
相关论文
共 50 条
[1]
Platelet-activating factor concentration in the stool of human newborns: Effects of enteral feeding and neonatal necrotizing enterocolitis [J].
Amer, MD ;
Hedlund, E ;
Rochester, J ;
Caplan, MS .
BIOLOGY OF THE NEONATE, 2004, 85 (03) :159-166
[2]
Postoperative outcomes of extremely low birth-weight infants with necrotizing enterocolitis or isolated intestinal perforation - A prospective cohort study by the NICHD neonatal research network [J].
Blakely, ML ;
Lally, KP ;
McDonald, S ;
Brown, RL ;
Barnhart, DC ;
Ricketts, RR ;
Thompson, WR ;
Scherer, LR ;
Klein, MD ;
Letton, RW ;
Chwals, WJ ;
Touloukian, RJ ;
Kurkchubasche, AG ;
Skinner, MA ;
Moss, RL ;
Hilfiker, ML .
ANNALS OF SURGERY, 2005, 241 (06) :984-989
[3]
NOD2-associated diseases: Bridging innate immunity and autoinflammation [J].
Borzutzky, Arturo ;
Fried, Ari ;
Chou, Janet ;
Bonilla, Francisco A. ;
Kim, Susan ;
Dedeoglu, Fatma .
CLINICAL IMMUNOLOGY, 2010, 134 (03) :251-261
[4]
The role of recombinant platelet-activating factor acetylhydrolase in a neonatal rat model of necrotizing enterocolitis [J].
Caplan, MS ;
Lickerman, M ;
Adler, L ;
Dietsch, GN ;
Yu, A .
PEDIATRIC RESEARCH, 1997, 42 (06) :779-783
[5]
The platelet-activating factor receptor antagonist WEB 2170 prevents neonatal necrotizing enterocolitis in rats [J].
Caplan, MS ;
Hedlund, E ;
Adler, L ;
Lickerman, M ;
Hsueh, W .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 1997, 24 (03) :296-301
[6]
Caradonna L, 2000, AM J GASTROENTEROL, V95, P1495
[7]
Endotoxin inhibits intestinal epithelial restitution through activation of Rho-GTPase and increased focal adhesions [J].
Cetin, S ;
Ford, HR ;
Sysko, LR ;
Agarwal, C ;
Wang, J ;
Neal, MD ;
Baty, C ;
Apodaca, G ;
Hackam, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (23) :24592-24600
[8]
Role of LPS/CD14/TLR4-mediated inflammation in necrotizing enterocolitis: Pathogenesis and therapeutic implications [J].
Chan, Kwong L. ;
Wong, Kwong F. ;
Luk, John M. .
WORLD JOURNAL OF GASTROENTEROLOGY, 2009, 15 (38) :4745-4752
[9]
Extracellular High Mobility Group Box-1 (HMGB1) Inhibits Enterocyte Migration via Activation of Toll-like Receptor-4 and Increased Cell-Matrix Adhesiveness [J].
Dai, Shipan ;
Sodhi, Chhinder ;
Cetin, Selma ;
Richardson, Ward ;
Branca, Maria ;
Neal, Matthew D. ;
Prindle, Thomas ;
Ma, Congrong ;
Shapiro, Richard A. ;
Li, Bin ;
Wang, James H. -C. ;
Hackam, David J. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (07) :4995-5002
[10]
Concordance of bacterial cultures with endotoxin and interleukin-6 in necrotizing enterocolitis [J].
Duffy, LC ;
Zielezny, MA ;
Carrion, V ;
Griffiths, E ;
Dryja, D ;
Hilty, M ;
Rook, C ;
Morin, F .
DIGESTIVE DISEASES AND SCIENCES, 1997, 42 (02) :359-365