Toll-like receptor polymorphisms and tuberculosis susceptibility: A comprehensive meta-analysis

Author(s):  
Qin Sun ◽  
Qing Zhang ◽  
He-ping Xiao ◽  
Chong Bai
PLoS ONE ◽  
2013 ◽  
Vol 8 (5) ◽  
pp. e63357 ◽  
Author(s):  
Yuxiang Zhang ◽  
Tingting Jiang ◽  
Xiuyun Yang ◽  
Yun Xue ◽  
Chong Wang ◽  
...  

2013 ◽  
Vol 49 (8) ◽  
pp. 2068-2070 ◽  
Author(s):  
Xinxin Zhao ◽  
Lingling Liu ◽  
Shan Kang ◽  
Dongfeng Zhang

2011 ◽  
Vol 39 (4) ◽  
pp. 3393-3400 ◽  
Author(s):  
Qin Wang ◽  
Ping Zhan ◽  
Li-Xin Qiu ◽  
Qian Qian ◽  
Li-Ke Yu

2011 ◽  
Vol 10 (12) ◽  
pp. 790-792 ◽  
Author(s):  
Lorena Alvarez-Rodriguez ◽  
Pedro Muñoz Cacho ◽  
Marcos Lopez-Hoyos ◽  
Ignacio Beares ◽  
Cristina Mata ◽  
...  

2018 ◽  
Vol 146 (5) ◽  
pp. 642-647 ◽  
Author(s):  
Xiaochun Jin ◽  
Shuzhou Yin ◽  
Youtao Zhang ◽  
Xu Chen

AbstractToll-like receptor 2 (TLR2) is a key member of TLRs, which is crucial in the initial inflammatory response against bacteria. TLR2, is also the initial barrier against bacterial infection and plays an important role in recognising a variety of bacterial lipoproteins. Several studies have been performed to investigate the TLR2 + 2477G/A polymorphism and bacterial meningitis susceptibility. Unfortunately, the results of previous studies were controversial. Therefore, we performed a meta-analysis to derive a more precise estimation of the association. The association between the TLR2 + 2477G/A polymorphism and bacterial meningitis susceptibility was assessed by odds ratios together with their 95% confidence intervals (CI). Six studies were enrolled in the present meta-analysis. Overall, no significant association between TLR2 + 2477G/A polymorphism and bacterial meningitis risk were found under allele contrast (A vs. G: OR = 1.15, 95% CI = 0.93–1.43, P = 0.202), recessive genetic model (AA vs. AG/GG: OR = 1.12, 95% CI = 0.90–1.41, P = 0.313). The significant association was found between TLR2 + 2477G/A polymorphism and pneumococcal meningitis risk under allele contrast (A vs. G: OR = 1.54, 95% CI = 1.01–2.36, P = 0.046), recessive genetic model (AA vs. AG/GG: OR = 1.63, 95% CI = 1.03–2.57, P = 0.035). We conclude that TLR2 + 2477G/A polymorphism is not associated with meningococcal meningitis risk but contributes an increased risk of pneumococcal meningitis.


2012 ◽  
Vol 40 (4) ◽  
pp. 3015-3020 ◽  
Author(s):  
F. S. Belforte ◽  
F. Coluccio Leskow ◽  
E. Poskus ◽  
A. Penas Steinhardt

2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Hwa Chia Chai ◽  
Kek Heng Chua ◽  
Soo Kun Lim ◽  
Maude Elvira Phipps

Polymorphisms in genes involved in toll-like receptor/interferon signalling pathways have been reported previously to be associated with SLE in many populations. This study aimed to investigate the role of seven single nucleotide polymorphisms withinTNFAIP3,STAT4,andIRF5, which are involved in upstream and downstream pathways of type I interferon production, in SLE in the South East Asian populations. Genotyping of 360 Malaysian SLE patients and 430 normal healthy individuals revealed that minor alleles ofSTAT4rs7574865 and rs10168266 were associated with elevated risk of SLE in the Chinese and Malay patients, respectively (P=0.028, odds ratio(OR)=1.42;P=0.035,OR=1.80, respectively). Polymorphisms inTNFAIP3andIRF5did not show significant associations with SLE in any of the ethnicities. Combined analysis of the Malays, Chinese, and Indians for each SNP indicated thatSTAT4rs10168266 was significantly associated with the Malaysian SLE as a whole (P=0.014;OR=1.435). The meta-analysis ofSTAT4rs10168266, which combined the data of other studies and this study, further confirmed its importance as the risk factor for SLE by having pooled OR of 1.559 andPvalue of <0.001.


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