首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Killer Immunoglobulin-Like Receptor 2DS2 (KIR2DS2) KIR2DL2-HLA-C1 and KIR2DL3 as Genetic Markers for Stratifying the Risk of Cytomegalovirus Infection in Kidney Transplant Recipients
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Killer Immunoglobulin-Like Receptor 2DS2 (KIR2DS2) KIR2DL2-HLA-C1 and KIR2DL3 as Genetic Markers for Stratifying the Risk of Cytomegalovirus Infection in Kidney Transplant Recipients

机译:致死性免疫球蛋白样受体2DS2(KIR2DS2)KIR2DL2-HLA-C1和KIR2DL3作为遗传标记可用于确定肾脏移植受者巨细胞病毒感染的风险

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摘要

Infection with cytomegalovirus (CMV) remains a major problem in kidney transplant recipients, resulting in serious infectious complications and occasionally mortality. Accumulating evidence indicates that natural killer cell immunoglobulin-like receptors (KIRs) and their ligands affect the susceptibility to various diseases, including viral infections (e.g., CMV infection). We investigated whether KIR genes and their ligands affect the occurrence of CMV infection in a group of 138 kidney transplant recipients who were observed for 720 days posttransplantation. We typed the recipients for the presence of KIR genes (human leukocyte antigen C1 [HLA-C1], HLA-C2, HLA-A, HLA-B, and HLA-DR1) by polymerase chain reaction with sequence-specific primers. The multivariate analysis revealed that the lack of KIR2DS2 (p = 0.035), the presence of KIR2DL3 (p = 0.075), and the presence of KIR2DL2–HLA-C1 (p = 0.044) were risk factors for posttransplant CMV infection. We also found that a lower estimated glomerular filtration rate (p = 0.036), an earlier time of antiviral prophylaxis initiation (p = 0.025), lymphocytopenia (p = 0.012), and pretransplant serostatus (donor-positive/recipient-negative; p = 0.042) were independent risk factors for posttransplant CMV infection. In conclusion, our findings confirm that the KIR/HLA genotype plays a significant role in anti-CMV immunity and suggest the contribution of both environmental and genetic factors to the incidence of CMV infection after kidney transplantation.
机译:巨细胞病毒(CMV)感染仍然是肾移植受者中的主要问题,导致严重的感染并发症和偶发性死亡。越来越多的证据表明,天然杀伤细胞免疫球蛋白样受体(KIR)及其配体会影响对各种疾病的敏感性,包括病毒感染(例如CMV感染)。我们调查了KIR基因及其配体是否影响了在移植后720天观察的一组138位肾移植受者中CMV感染的发生。我们通过与序列特异性引物的聚合酶链反应,为KIR基因(人类白细胞抗原C1 [HLA-C1],HLA-C2,HLA-A,HLA-B和HLA-DR1)的存在键入了受体。多元分析表明,缺乏KIR2DS2(p = 0.035),存在KIR2DL3(p = 0.075)和存在KIR2DL2-HLA-C1(p = 0.044)是移植后CMV感染的危险因素。我们还发现较低的估计肾小球滤过率(p = 0.036),较早的抗病毒预防启动时间(p = 0.025),淋巴细胞减少(p = 0.012)和移植前血清状态(供体阳性/受体阴性; p = 0.042)是移植后CMV感染的独立危险因素。总之,我们的发现证实了KIR / HLA基因型在抗CMV免疫中起着重要作用,并暗示了环境和遗传因素对肾脏移植后CMV感染发生率的贡献。

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