Polymorphisms in the toll-like receptor 9 gene associated with sepsis and multiple organ dysfunction after major blunt trauma

被引:30
作者
Chen, K. -H. [1 ]
Zeng, L. [1 ]
Gu, W. [1 ]
Zhou, J. [2 ]
Du, D. -Y. [3 ]
Jiang, J. -X. [1 ]
机构
[1] Third Mil Med Univ, Daping Hosp, Inst Surg Res, State Key Lab Trauma Burns & Combined Injury, Chongqing 400042, Peoples R China
[2] Third Mil Med Univ, Daping Hosp, Dept Traumat Surg, Chongqing 400042, Peoples R China
[3] Chongqing Emergency Med Ctr, Chongqing, Peoples R China
关键词
SINGLE-NUCLEOTIDE POLYMORPHISMS; SYSTEMIC-LUPUS-ERYTHEMATOSUS; DNA; POPULATION; ACTIVATION; HAPLOTYPES; TLR9;
D O I
10.1002/bjs.7532
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Toll-like receptor (TLR) 9 is the pattern recognition receptor for microbial DNA. Genetic variation within pattern recognition receptors for bacterial endotoxin and exotoxin has been shown to be associated with the risk of sepsis and organ dysfunction in critical illness. However, little is known about the clinical relevance of TLR9 gene polymorphisms in critical illness. Methods: A total of 557 patients with major blunt trauma were included in the study. Genetic variation data for the entire TLR9 gene were obtained from the HapMap Project. The genotypes of TLR9 gene polymorphisms were determined using a pyrosequencing method. Whole peripheral blood samples obtained immediately after admission were stimulated with bacterial DNA and production of tumour necrosis factor (TNF) alpha was then determined. Sepsis morbidity rate and multiple organ dysfunction (MOD) scores were assessed. Results: Of five single-nucleotide polymorphisms (SNPs) genotyped, four (rs187084, rs352139, rs352140 and rs352162) existed as common SNPs and were in strong linkage disequilibrium. Both rs187084 and rs352162 were significantly associated with TNF-alpha production by peripheral blood leucocytes in response to bacterial DNA stimulation and a higher sepsis morbidity rate in patients with major trauma. In addition, the rs352162 polymorphism was significantly associated with MOD scores, whereas rs187084 showed a trend to be associated with MOD score. Conclusion: TLR9 polymorphisms rs187084 and rs352162 might be used to provide relevant risk estimates for the development of sepsis and MOD in patients with major trauma.
引用
收藏
页码:1252 / 1259
页数:8
相关论文
共 23 条
[1]   TLR9-Dependent Activation of Dendritic Cells by DNA from Leishmania major Favors Th1 Cell Development and the Resolution of Lesions [J].
Abou Fakher, Faihaa Hkima ;
Rachinel, Nicolas ;
Klimczak, Martine ;
Louis, Jacques ;
Doyen, Noelle .
JOURNAL OF IMMUNOLOGY, 2009, 182 (03) :1386-1396
[2]   Determination of single-nucleotide polymorphisms by real-time pyrophosphate DNA sequencing [J].
Alderborn, A ;
Kristofferson, A ;
Hammerling, U .
GENOME RESEARCH, 2000, 10 (08) :1249-1258
[3]  
*ASS ADV AUT MED, ABBR INJ SCAL 2005 R
[4]   Expression and function of Toll-like receptor 9 in severely injured patients prone to sepsis [J].
Baiyee, E. E. ;
Flohe, S. ;
Lendemans, S. ;
Bauer, S. ;
Mueller, N. ;
Kreuzfelder, E. ;
Grosse-Wilde, H. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2006, 145 (03) :456-462
[5]   The association of innate immune response gene polymorphisms and puerperal group A streptococcal sepsis [J].
Davis, Sarah M. ;
Clark, Erin A. S. ;
Nelson, Lesa T. ;
Silver, Robert M. .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2010, 202 (03) :308.e1-308.e8
[6]  
Dupont W D., Ps Power and Sample Size Program
[7]   BCR-mediated uptake of antigen linked to TLR9 ligand stimulates B-cell proliferation and antigen-specific plasma cell formation [J].
Eckl-Dorna, Julia ;
Batista, Facundo D. .
BLOOD, 2009, 113 (17) :3969-3977
[8]  
ETEM EO, 2010, RHEUMATOL INT
[9]   Functional significance of gene polymorphisms in the promoter of myeloid differentiation-2 [J].
Gu, Wei ;
Shan, You-an ;
Zhou, Jian ;
Jiang, Dong-po ;
Zhang, Lianyang ;
Du, Ding-Yuan ;
Wang, Zheng-guo ;
Jiang, Jian-xin .
ANNALS OF SURGERY, 2007, 246 (01) :151-158
[10]   A Toll-like receptor recognizes bacterial DNA [J].
Hemmi, H ;
Takeuchi, O ;
Kawai, T ;
Kaisho, T ;
Sato, S ;
Sanjo, H ;
Matsumoto, M ;
Hoshino, K ;
Wagner, H ;
Takeda, K ;
Akira, S .
NATURE, 2000, 408 (6813) :740-745