Tawfeek Gehan Abd-Elfatah, Alhassanin Suzan
a Clinical Pathology Department, Faculty of Medicine , Menoufia University , Al Minufiyah , Egypt.
b Clinical Oncology Department, Faculty of Medicine , Menoufia University , Al Minufiyah , Egypt.
Immunol Invest. 2018 Apr;47(3):315-325. doi: 10.1080/08820139.2018.1430826. Epub 2018 Feb 1.
Non-Hodgkin lymphoma (NHL) is a major cancer in Egypt and worldwide and has many risk factors including genes involved in the immune response.
we investigated the HLA-G 14bp gene polymorphism as a risk factor for NHL and its clinic pathologic features. The study involved 150 patients with NHL and 100 healthy control. Full histories, clinical examination, C.T scan and laboratory investigations such as CBC, LDH, ?2microglobulin and HCV RNA by qualitative real time PCR were performed for all subjects. HLA-G 14bp ins/del gene polymorphism was determined by PCR.
in our study, del/del, ins/del and dominant genotypes increased the risk of NHL by 11.01, 10.55 and 10.88 fold respectively (p<0.001) but the recessive genotype did not increase the risk of NHL (p=0.112). Cases with the del allele had a greater risk of NHL than those with the ins allele (p<0.001). del/del and ins/del genotypes were significantly associated with higher LDH and ?2microglobulin levels (p<0.001), lower Hb and platelet values (p<0.001), extra nodal sites (p=0.001), poor performance status (p=0.04) and relapse (p=0.001). Conclusions: the results suggest that HLA-G 14bp ins/del gene polymorphism is a risk factor for NHL in our Egyptian population and is associated with poor clinical pathological features.
Non-Hodgkin lymphoma (NHL), Diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL), Epstein-Barr virus (EBV), human T-cell lymphotropic/leukemia virus-1 (HTLV-1).
非霍奇金淋巴瘤(NHL)是埃及和全球范围内的一种主要癌症,有许多风险因素,包括参与免疫反应的基因。
我们研究了HLA - G 14bp基因多态性作为NHL的一个风险因素及其临床病理特征。该研究纳入了150例NHL患者和100名健康对照者。对所有受试者进行了全面病史、临床检查、CT扫描以及实验室检查,如血常规、乳酸脱氢酶(LDH)、β2微球蛋白和通过实时定量PCR检测丙型肝炎病毒RNA。通过PCR确定HLA - G 14bp插入/缺失基因多态性。
在我们的研究中,缺失/缺失、插入/缺失和显性基因型使NHL风险分别增加了11.01倍、10.55倍和10.88倍(p<0.001),但隐性基因型并未增加NHL风险(p = 0.112)。携带缺失等位基因的病例患NHL的风险高于携带插入等位基因的病例(p<0.001)。缺失/缺失和插入/缺失基因型与较高的LDH和β2微球蛋白水平显著相关(p<0.001),与较低的血红蛋白和血小板值显著相关(p<0.001),与结外部位(p = 0.001)、较差的体能状态(p = 0.04)和复发(p = 0.001)显著相关。结论:结果表明,HLA - G 14bp插入/缺失基因多态性是我们埃及人群中NHL的一个风险因素,并且与不良临床病理特征相关。
非霍奇金淋巴瘤(NHL)、弥漫性大B细胞淋巴瘤(DLBCL)、滤泡性淋巴瘤(FL)、爱泼斯坦 - 巴尔病毒(EBV)、人类嗜T淋巴细胞病毒1型(HTLV - 1)