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KIR 和 HLA 相互作用与实体器官移植受者原发性 CMV 感染的控制有关。

KIR and HLA interactions are associated with control of primary CMV infection in solid organ transplant recipients.

出版信息

Am J Transplant. 2014 Jan;14(1):156-62. doi: 10.1111/ajt.12532.

Abstract

Cytomegalovirus (CMV) infection remains a major source of morbidity and mortality in solid organ transplant recipients. Killer immunoglobulin-like receptors(KIR) are genetically polymorphic natural killer(NK) cell receptors important in antiviral responses. A retrospective, single-center cohort study was performed to study the interaction of KIR genotype and primary control of CMV infection after transplantation.Time to first CMV viremia was determined for a cohort of 531 CMV serology donor positive/recipient negative solid organ transplant recipients. Of the KIR genes,KIR2DL3 and KIR2DS2 were most strongly associated with time to CMV viremia in random survival forest analysis. As KIR2DL3 and KIR2DS2 both interact with HLA-C1, these interactions were evaluated. Seventy six recipients were found to be positive for both KIR2DL3 and KIR2DS2 and expressed only HLA-C1 antigens in both recipient and donor. These patients had a substantially reduced hazard of CMV viremia in the first year after solid organ transplantation (hazard ratio 0.44, 95% CI 0.27–0.72, p=0.0012). In KIR2DL3+/KIR2DS2+/HLA-C1/1 recipients who received an organ from a non-C1/1 donor, this protective effect was not observed. These results improve our understanding of human NK cell function in primary CMV infection after transplant.

摘要

巨细胞病毒(CMV)感染仍然是实体器官移植受者发病率和死亡率的主要原因。细胞毒性免疫球蛋白样受体(KIR)是遗传多态性天然杀伤(NK)细胞受体,在抗病毒反应中很重要。进行了一项回顾性、单中心队列研究,以研究移植后 KIR 基因型和 CMV 感染的主要控制之间的相互作用。对 531 例 CMV 血清学供体阳性/受体阴性实体器官移植受者的队列进行了首次 CMV 血症时间的研究。在随机生存森林分析中,KIR 基因中 KIR2DL3 和 KIR2DS2 与 CMV 病毒血症时间最密切相关。由于 KIR2DL3 和 KIR2DS2 均与 HLA-C1 相互作用,因此评估了这些相互作用。发现 76 例受者同时为 KIR2DL3 和 KIR2DS2 阳性,并且在受者和供者中仅表达 HLA-C1 抗原。这些患者在实体器官移植后第一年 CMV 病毒血症的风险显著降低(危险比 0.44,95%CI 0.27-0.72,p=0.0012)。在 KIR2DL3+/KIR2DS2+/HLA-C1/1 受者中,如果接受非 C1/1 供体的器官,则未观察到这种保护作用。这些结果提高了我们对移植后原发性 CMV 感染中人类 NK 细胞功能的理解。

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