Wei Jingjing, Kurumi Hiroki, Isomoto Hajime, Ogihara Ryohei, Matsushima Kayoko, Machida Haruhisa, Ishida Tetsuya, Hirayama Tatsuro, Yamaguchi Naoyuki, Yoshida Yukina, Tsukamoto Kazuhiro
Department of Endoscopy, The First Affiliated Hospital of Fujian Medical University, Fuzhou 350004, China.
Department of Endoscopy, National Regional Medical Center, Binhai Campus of the First Affiliated Hospital of Fujian Medical University, Fuzhou 350212, China.
Diagnostics (Basel). 2025 Apr 10;15(8):971. doi: 10.3390/diagnostics15080971.
: To explore the possible relationship between Toll-like receptor (TLR) gene encoding and a predictive outcome for the loss of response (LOR) to IFX treatment among Japanese patients with Crohn's disease (CD). : An association analysis that involved 25 single-nucleotide polymorphisms (SNPs) across the TLR1, TLR2, TLR4, TLR6, TLR9, and TLR10 genes was performed on a cohort of 127 Japanese patients with CD. The therapeutic responses were evaluated at 10 weeks, 1 year, and 2 years using three different inheritance models. : The CD patients with a G/G genotype of rs5743565 in TLR1 were significantly less likely in the responders at 10 weeks compared with the non-responders ( = 0.023, OR = 0.206). The frequencies of the C/T or T/T genotypes of rs5743604 in the TLR1, G/A, or A/A genotypes of rs13105517 in TLR2, both in the minor allele dominant model, were significantly higher in the responders at 10 weeks as compared with those in the non-responders ( = 0.035, OR = 4.401; = 0.017, OR = 5.473). The patients with an A/A genotype of rs13105517 in TLR2 in the minor allele recessive model were significantly less likely in the responders at one year of IFX treatment compared with those in the non-responders ( = 0.004, OR = 0.195). : The polymorphisms of TLR1 and TLR2 can be useful as biomarkers for predicting initial and secondary LOR to IFX in Japanese CD patients. The IFX response in genetic testing may target molecules for new drugs to overcome the non-response and LOR to IFX.
探讨日本克罗恩病(CD)患者中Toll样受体(TLR)基因编码与英夫利昔单抗(IFX)治疗反应丧失(LOR)预测结果之间的可能关系。
对127例日本CD患者队列进行关联分析,涉及TLR1、TLR2、TLR4、TLR6、TLR9和TLR10基因的25个单核苷酸多态性(SNP)。使用三种不同的遗传模型在10周、1年和2年时评估治疗反应。
TLR1中rs5743565的G/G基因型CD患者在10周时应答者的可能性明显低于无应答者(P=0.023,OR=0.206)。在次要等位基因显性模型中,TLR1中rs5743604的C/T或T/T基因型、TLR2中rs13105517的G/A或A/A基因型在10周时应答者中的频率显著高于无应答者(P=0.035,OR=4.401;P=0.017,OR=5.473)。在次要等位基因隐性模型中,TLR2中rs13105517的A/A基因型患者在IFX治疗1年时应答者的可能性明显低于无应答者(P=0.004,OR=0.195)。
TLR1和TLR2的多态性可作为预测日本CD患者对IFX初始和继发性LOR的生物标志物。基因检测中的IFX反应可能为新药靶向分子,以克服对IFX的无反应和LOR。