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Association of TNF-alpha, TGF-beta 1, IL-10, IL-6, and IFN-gamma gene polymorphism with acute rejection and infection in lung transplant recipients

机译:TNF-α,TGF-β1,IL-10,IL-6和IFN-γ基因多态性与肺移植受者急性排斥反应和感染的关系

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摘要

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- (-308 A/G), TGF-1 (+869 T/C, +915 G/C), IL-10 (-592 C/A, -819 T/C, -1082 G/A), IL-6 (-174 G/C), and IFN- (+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 ((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.
机译:感染和排斥是肺移植受者(LTR)面临的常见并发症,并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中起重要作用。在这项研究中,我们探讨了TNF-(-308 A / G),TGF-1(+869 T / C,+ 915 G / C),IL-10(-592 C / A,-819 T / C,-1082 G / A),IL-6(-174 G / C)和IFN-(+874 T / A)基因多态性以及急性排斥和感染的发生率。在2004年12月至2012年11月期间,回顾性队列研究了来自单个中心的113个LTR的移植结局。使用基于序列特异性引物的PCR测量细胞因子多态性。对捐赠者和接受者进行HLA分型。我们发现具有IL-10 -819 CC和-592 CC基因型的LTR具有显着降低的感染风险(p = 0.017,OR = 0.177,95%CI = 0.04-0.85)。但是,我们发现细胞因子多态性与急性排斥反应之间无显着关联。此外,数据显示急性排斥反应的发生与感染发作密切相关((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LTR可能受到保护,以免发生感染。我们的结果表明,感染是LTR急性排斥的重要原因。

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