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Age and cellular composition influence overall survival in a collective of non-immunocompromised patients with EBV-positive diffuse large B-cell lymphoma from a German lymphoma center

机译:年龄和细胞组成会影响来自德国淋巴瘤中心的一组非免疫妥协的EBV阳性弥漫性大B细胞淋巴瘤患者的总体生存

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We investigated 41 diffuse large B-cell lymphomas (DLBCL) diagnosed at one center harboring >= 50% of latently Epstein-Barr virus (EBV)-infected neoplastic cells occurring in 34 patients aged >= 50 years and in 7 patients younger than 50 years in the absence of any known immunodeficiency for the expression patterns of EBV latent and immediate-early proteins, for the differentiation stage of the neoplastic cells, the presence of cytogenetic alterations and a possible co-infection with the human herpes virus (HHV)-8. Here, we show that EBV-positive DLBCLs rarely arise from naive and more frequently from post-germinal center B-cells that often contain crippling immunoglobulin gene mutations. Most of the lymphomas did not exhibit breaks in the BCL2, BCL6, and MYC genes and none of the cases investigated contained HHV-8 sequences. Patients aged <50 years performed better than older ones while in patients aged >= 50 years only the cellular composition had an impact on overall survival.
机译:我们调查了在一个中心诊断出的41例弥漫性大B细胞淋巴瘤(DLBCL),其中> = 50岁的34例患者和年龄小于50岁的7例患者中感染了50%的潜在爱泼斯坦-巴尔病毒(EBV)感染的肿瘤细胞多年以来,尚无任何已知的EBV潜伏蛋白和即早蛋白质表达模式,肿瘤细胞分化阶段,细胞遗传学改变以及可能与人疱疹病毒(HHV)共同感染的免疫缺陷病- 8。在这里,我们显示EBV阳性DLBCLs很少来自幼稚的地方,而更常见的是来自萌发后的中枢B细胞,后者通常包含严重的免疫球蛋白基因突变。大多数淋巴瘤在BCL2,BCL6和MYC基因上均未出现断裂,所调查的病例均未包含​​HHV-8序列。 <50岁的患者比老年患者表现更好,而> = 50岁的患者仅细胞组成对总体存活率有影响。

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