Mu Hui-Jun, Xie Ping, Chen Jing-Yu, Gao Fei, Zou Jian, Zhang Ji, Zhang Bin
Department of Clinical Laboratory Science, Wuxi People's Hospital affiliated to Nanjing Medical University, Wuxi, China; Jiangsu Key laboratory of Organ Transplantation, Wuxi, China.
Clin Transplant. 2014 Sep;28(9):1016-24. doi: 10.1111/ctr.12411. Epub 2014 Jul 24.
Infection and rejection are common complications faced by lung transplant recipients (LTRs) and have become major impediments to long-term survival. Cytokines may play an important role in the development of these complications. In this study, we explored the correlation between TNF-α (-308 A/G), TGF-β1 (+869 T/C, +915 G/C), IL-10 (-592 C/A, -819 T/C, -1082 G/A), IL-6 (-174 G/C), and IFN-γ (+874 T/A) gene polymorphisms and the incidence of acute rejection and infection. Transplant outcomes were reviewed in a retrospective cohort of 113 LTRs from a single center between December 2004 and November 2012. Cytokine polymorphisms were measured using sequence-specific primer-based PCR. HLA typing was performed for the donors and recipients. We found that the LTRs with the IL-10 -819 CC and -592 CC genotypes had a significantly decreased risk of infection (p = 0.017, OR = 0.177, 95% CI = 0.04-0.85). However, we found no significant association between cytokine polymorphisms and acute rejection. Furthermore, the data revealed that the occurrence of acute rejection was strongly associated with infection episodes (χ(2) = 8.5256, p < 0.01). These results suggest that LTRs possessing the IL-10 -819 CC and -592 CC genotype may be protected from the occurrence of infection. Our results demonstrated that infection is an important cause of acute rejection for LTRs.
感染和排斥反应是肺移植受者(LTRs)常见的并发症,已成为长期生存的主要障碍。细胞因子可能在这些并发症的发生发展中起重要作用。在本研究中,我们探讨了肿瘤坏死因子-α(TNF-α,-308 A/G)、转化生长因子-β1(TGF-β1,+869 T/C、+915 G/C)、白细胞介素-10(IL-10,-592 C/A、-819 T/C、-1082 G/A)、白细胞介素-6(IL-6,-174 G/C)和干扰素-γ(IFN-γ,+874 T/A)基因多态性与急性排斥反应和感染发生率之间的相关性。回顾性分析了2004年12月至2012年11月来自单一中心的113例LTRs队列的移植结局。采用序列特异性引物PCR检测细胞因子多态性。对供体和受体进行HLA分型。我们发现,IL-10 -819 CC和-592 CC基因型的LTRs感染风险显著降低(p = 0.017,OR = 0.177,95% CI = 0.04-0.85)。然而,我们未发现细胞因子多态性与急性排斥反应之间存在显著关联。此外,数据显示急性排斥反应的发生与感染发作密切相关(χ(2) = 8.5256,p < 0.01)。这些结果表明,具有IL-10 -819 CC和-592 CC基因型的LTRs可能免受感染的发生。我们的结果表明,感染是LTRs急性排斥反应的重要原因。