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艾滋病相关淋巴瘤的肿瘤病毒格局

The tumor virus landscape of AIDS-related lymphomas.

作者信息

Arvey Aaron, Ojesina Akinyemi I, Pedamallu Chandra Sekhar, Ballon Gianna, Jung Joonil, Duke Fujiko, Leoncini Lorenzo, De Falco Giulia, Bressman Eric, Tam Wayne, Chadburn Amy, Meyerson Matthew, Cesarman Ethel

机构信息

Department of Immunology and Microbial Pathogenesis, Memorial Sloan-Kettering Cancer Center, New York, NY;

Cancer Program, Broad Institute of MIT and Harvard, Cambridge, MA; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA;

出版信息

Blood. 2015 May 14;125(20):e14-22. doi: 10.1182/blood-2014-11-599951. Epub 2015 Mar 31.

Abstract

Immunodeficiency dramatically increases susceptibility to cancer as a result of reduced immune surveillance and enhanced opportunities for virus-mediated oncogenesis. Although AIDS-related lymphomas (ARLs) are frequently associated with known oncogenic viruses, many cases contain no known transforming virus. To discover novel transforming viruses, we profiled a set of ARL samples using whole transcriptome sequencing. We determined that Epstein-Barr virus (EBV) was the only virus detected in the tumor samples of this cohort, suggesting that if unidentified pathogens exist in this disease, they are present in <10% of cases or undetectable by our methods. To evaluate the role of EBV in ARL pathogenesis, we analyzed viral gene expression and found highly heterogeneous patterns of viral transcription across samples. We also found significant heterogeneity of viral antigen expression across a large cohort, with many patient samples presenting with restricted type I viral latency, indicating that EBV latency proteins are under increased immunosurveillance in the post-combined antiretroviral therapies era. Furthermore, EBV infection of lymphoma cells in HIV-positive individuals was associated with a distinct host gene expression program. These findings provide insight into the joint host-virus regulatory network of primary ARL tumor samples and expand our understanding of virus-associated oncogenesis. Our findings may also have therapeutic implications, as treatment may be personalized to target specific viral and virus-associated host processes that are only present in a subset of patients.

摘要

免疫缺陷会因免疫监视功能降低以及病毒介导的肿瘤发生机会增加而显著提高患癌易感性。尽管艾滋病相关淋巴瘤(ARL)常与已知致癌病毒有关,但许多病例中并未发现已知的转化病毒。为了发现新型转化病毒,我们使用全转录组测序对一组ARL样本进行了分析。我们确定,爱泼斯坦-巴尔病毒(EBV)是该队列肿瘤样本中检测到的唯一病毒,这表明如果该疾病中存在未识别的病原体,那么它们在不到10%的病例中存在,或者用我们的方法无法检测到。为了评估EBV在ARL发病机制中的作用,我们分析了病毒基因表达,发现样本间病毒转录模式高度异质性。我们还发现,在一大群患者中,病毒抗原表达存在显著异质性,许多患者样本呈现I型病毒潜伏期受限,这表明在联合抗逆转录病毒治疗时代,EBV潜伏期蛋白受到了更强的免疫监视。此外,HIV阳性个体中淋巴瘤细胞的EBV感染与独特的宿主基因表达程序相关。这些发现为原发性ARL肿瘤样本的宿主-病毒联合调控网络提供了见解,并扩展了我们对病毒相关肿瘤发生的理解。我们的发现也可能具有治疗意义,因为治疗可能会针对仅在一部分患者中存在的特定病毒及病毒相关宿主过程进行个性化定制。

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