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Blood Epstein-Barr virus DNA load and risk of progression to AIDS-related systemic B lymphoma

机译:血液爱泼斯坦-巴尔病毒DNA负载和发展为AIDS相关的系统性B淋巴瘤的风险

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Background: AIDS-related lymphoma (ARL) remains the main cause of AIDS-related deaths in the combined antiretroviral therapy (cART) era. Although most ARLs are associated with the Epstein-Barr virus (EBV), whether patients with high EBV burden are more at risk of developing ARL is unknown. This study investigated the relationship between high blood EBV DNA loads and subsequent progression to ARL. Methods: We identified 43 cases of ARL diagnosed between 1988 and 2007 within two cohorts (ANRS SEROCO/HEMOCO and PRIMO) and for which stored serum and peripheral blood mononuclear cell (PBMC) samples were available within 3 years before ARL diagnosis. For each case, two controls matched for the cohort and CD4 cell count in the year of ARL diagnosis were selected. EBV DNA was measured in PBMCs and serum samples with a commercial kit. Results: High levels of EBV DNA in PBMCs collected a median of 10 months before diagnosis were associated with an increased risk of developing systemic B lymphoma (adjusted odds ratio 2.47; 95% confidence interval 1.15; 5.32 for each 1log copies/10 6 PBMC increase in EBV load) but not with primary brain lymphoma. Conclusion: In this study, HIV-infected patients with undetectable EBV DNA in PBMCs did not develop ARL in the following 3 years, while high levels of EBV DNA in PBMCs predicted subsequent progression to systemic B lymphoma. Clinicians should be aware of the increased risk of developing systemic B lymphoma in HIV-infected patients with a high blood EBV DNA load.
机译:背景:在联合抗逆转录病毒疗法(cART)时代,艾滋病相关淋巴瘤(ARL)仍然是艾滋病相关死亡的主要原因。尽管大多数ARL与爱泼斯坦巴尔病毒(EBV)相关,但高EBV负担患者是否更容易患ARL。这项研究调查了高血EBV DNA负荷与随后发展为ARL之间的关系。方法:我们在两个队列(ANRS SEROCO / HEMOCO和PRIMO)中确定了1988年至2007年之间确诊的43例ARL病例,对于这些病例,在ARL诊断之前的3年内可获得血清和外周血单个核细胞(PBMC)样本。对于每种情况,选择两个在ARL诊断年匹配队列和CD4细胞计数的对照。使用商用试剂盒测量PBMC和血清样品中的EBV DNA。结果:在诊断前中位收集的PBMC中,EBMC DNA的高水平在诊断前10个月与发展为系统性B淋巴瘤的风险增加相关(校正比值比2.47; 95%置信区间1.15;每1log拷贝/ 10 6 PBMC增加5.32 EBV负荷),但不伴原发性脑淋巴瘤。结论:在这项研究中,HIV感染的PBMC中未检测到EBV DNA的患者在接下来的3年中没有发展为ARL,而PBMC中高水平的EBV DNA则预示了系统性B淋巴瘤的后续发展。临床医生应意识到,血液中EBV DNA负荷高的HIV感染患者发生全身性B淋巴瘤的风险增加。

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