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The Pre-/Post-Transplant Hepatitis C Antibody Associated with the IL-28B RS8099917 TT Genotype and miRNA-122 Expression May Protect Acute Cellular Rejection After LDLT.

作者信息

Chiu King-Wah, Lin Yu-Cheng, Li Wei-Feng, Huang Kuang-Tzu, Hsu Li-Wen, Wang Chih-Chi

机构信息

Division of Hepato-Gastroenterology, Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 83301, Taiwan.

Liver Transplantation Program, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 83301, Taiwan.

出版信息

Curr Issues Mol Biol. 2024 Nov 10;46(11):12772-12783. doi: 10.3390/cimb46110760.

Abstract

This study aimed to investigate the relationship between the IL-28B SNP rs8099917 genotype, miRNA-122 expression, and the immune mechanism of ACR after LT using anti-HCV antibody calibration. A total of 45 patients with HCV received LT. IL-28B SNP rs8099917 genotyping was used to divide patients into TT and GT groups. The relative expression levels of miRNA-122 were calculated by quantitative PCR. Anti-HCV titers before and after LT were tracked to observe the relationship with ACR. The ACR rates were 27.6% for genotype TT and 62.5% for genotype GT, indicating a significantly higher rate in the GT group compared to the TT group ( = 0.024). In the rs8099917 genotype, TT was significantly associated with higher serum miRNA-122 levels than GT ( < 0.001). The TT group had significantly better outcomes than the GT group ( = 0.005). The Mann-Whitney U test showed significant differences in pre-LT and post-LT anti-HCV titers between the IL-28B genotypes (TT and GT) ( values of 0.006 and 0.027, respectively). These results suggested that the IL-28B rs8099917 genotype TT may play a significant role in modulating immune responses, both in terms of anti-HCV titers and the risk of ACR, possibly mediated through miRNA-122 levels.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3545/11592417/5e19610bf86e/cimb-46-00760-g001.jpg

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引用本文的文献

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