慢性丙型肝炎患者KIR基因型对肝癌进展的影响

Livers Pub Date : 2023-07-31 DOI:10.3390/livers3030027
Waleed Abdelmaguid, Doha Maher, M. Kohla, S. Ezzat, I. Moaz, Wael S. Abdel-Mageed, K. El-Halfawy, M. Abdel-Rahman
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引用次数: 0

摘要

在埃及,肝细胞癌(HCC)是男性最常见的癌症,也是女性第二常见的癌症。此外,埃及是世界上丙型肝炎感染率最高的国家之一。本工作的目的是研究16个KIR基因在埃及慢性丙型肝炎病毒(HCV)感染者预后中的潜在作用。该研究是在IRB批准的方案下进行的。使用序列特异性引物聚合酶链式反应(SSP-PCR)对83名HCC患者、100名无HCC的慢性HCV感染患者和120名匹配的健康对照的外周血白细胞或非肿瘤肝脏中提取的种系DNA进行KIR基因分型。在83名HCC患者中,只有7名(8.4%)接受了干扰素和/或干扰素-利巴韦林联合治疗,其余患者中有50名(60.2%)未接受过HCV治疗,26名(31.3%)接受了直接作用抗病毒(DAA)治疗。我们的研究结果表明,与慢性HCV(27/100,27.0%)(p=0.0005,OR=0.21[0.08-0.53])和健康对照组(29/119,24.4%)(p=0.001,OR=0.24[0.09-0.61])相比,HCC患者(6/83,7.2%)中含有更多抑制性KIR基因和更少激活基因的KIR单倍型AA的发生率显著较低。此外,与慢性HCV(8/100,8.0%)(p=0.02,OR=2.7[1.11–6.79])和健康对照组(8/119,6.7%)(p=0.006,OR=3.31[1.35–8.16])相比,HCC患者(16/83,19.3%)中包含所有KIR基因的基因型6(G6)的频率显著较高慢性HCV患者(36/100,36%和34/100,34%),p分别为0.028和0.027。我们的结果与先前对HCV患者HCC的研究相反,这些患者大多接受干扰素治疗。总之,KIR单倍型AA在宿主防御HCC进展中具有重要作用,尤其是在接受DAA治疗的患者中,这表明KIR基因型状态对慢性HCV感染的结果具有重要作用。
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KIR Genotypes Impact Progression to Hepatocellular Carcinoma in Patients with Chronic Hepatitis C Infection
In Egypt, hepatocellular carcinoma (HCC) is the most prevalent cancer in men and the second most prevalent cancer in women. In addition, Egypt has one of the highest prevalences of hepatitis C infection in the world. The aim of the present work was to study the potential role of the 16 KIR genes in the outcome of individuals with chronic hepatitis C virus (HCV) infection in Egypt. The study was carried out under an IRB-approved protocol. Sequence-Specific-Primer-PCR (SSP-PCR) was used for KIR genotyping of germline DNA extracted from peripheral blood leukocytes or from the non-tumor liver of 83 HCC patients, 100 patients with chronic HCV infection without HCC, and 120 matched healthy controls. Out of the 83 HCC patients, only 7 (8.4%) were treated by interferon and/or interferon Ribavirin combination, while for the remaining patients 50 (60.2%) received no prior HCV therapy and 26 (31.3%) were treated with direct-acting antiviral (DAA). Our results showed that KIR haplotype AA that contains more inhibitory KIR genes and fewer activating genes was observed with a significantly lower frequency in HCC patients (6/83, 7.2%) compared to chronic HCV (27/100, 27.0%) (p = 0.0005, OR = 0.21 [0.08–0.53]) and healthy controls (29/119, 24.4%) (p = 0.001, OR = 0.24 [0.09–0.61]). In addition, the frequency of genotype 6 (G6) which contains all the KIR genes was significantly high in the HCC patients (16/83, 19.3%) compared to chronic HCV (8/100, 8.0%) (p = 0.02, OR = 2.7 [1.11–6.79]) and healthy controls (8/119, 6.7%) (p = 0.006, OR = 3.31 [1.35–8.16]). Activating KIR genes 2DS1 and 3DS1 were significantly higher in HCC patients (48/83, 57.83% and 45/83, 54.22%) compared to the chronic HCV patients (36/100, 36% and 34/100, 34%), p = 0.028, 0.027, respectively. Our results are contrary to a prior work on HCC from patients with HCV who were mostly treated by interferon-based therapies. In conclusion, KIR haplotype AA has an important role in host defense against HCC progression especially in patients treated by DAA, suggesting an important role of the KIR genotype status on the outcome of chronic HCV infection.
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