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爱泼斯坦-巴尔病毒的克隆性缺失潜伏膜蛋白1变体在欧洲结外NK/T细胞淋巴瘤中占主导地位,并在成功治疗过程中消失。

Clonal deleted latent membrane protein 1 variants of Epstein-Barr virus are predominant in European extranodal NK/T lymphomas and disappear during successful treatment.

作者信息

Halabi Mohamad Adnan, Jaccard Arnaud, Moulinas Rémi, Bahri Racha, Al Mouhammad Hazar, Mammari Nour, Feuillard Jean, Ranger-Rogez Sylvie

机构信息

Department of Microbiology, Faculty of Pharmacy, Limoges, France.

Department of Clinical Hematology, University Hospital Dupuytren, Limoges, France.

出版信息

Int J Cancer. 2016 Aug 15;139(4):793-802. doi: 10.1002/ijc.30128. Epub 2016 Apr 29.

Abstract

Extranodal natural killer/T-cell lymphomas (NK/TL), rare in Europe, are Epstein-Barr virus (EBV) associated lymphomas with poor outcomes. Here, we determined the virus type and analyzed the EBV latent membrane protein-1 (LMP1) gene sequence in NK/TL from French patients. Six clones of viral LMP1 were sequenced by Sanger technology in blood from 13 patients before treatment with an l-asparaginase based regimen and, for 8 of them, throughout the treatment. Blood LMP1 sequences from 21 patients without any known malignancy were tested as controls. EBV Type A was identified for 11/13 patients and for all controls. Before treatment, a clonal LMP1 gene containing a 30 bp deletion (del30) was found in 46.1% of NK/TL and only in 4.8% of controls. Treatment was less effective in these patients who died more rapidly than the others. Patients with a deleted strain evolving toward a wild-type strain during treatment reached complete remission. The LMP1 gene was sequenced by highly sensitive next-generation sequencing technology in five NK/TL nasopharyngeal biopsies, two of them originating from the previous patients. Del30 was present in 100% of the biopsies; two viruses at least coexisted in three biopsies. These results suggest that del30 may be associated with poor prognosis NK/TL and that strain evolution could be used as a potential marker to monitor treatment.

摘要

结外自然杀伤细胞/ T细胞淋巴瘤(NK/TL)在欧洲较为罕见,是与EB病毒(EBV)相关的淋巴瘤,预后较差。在此,我们确定了病毒类型,并分析了法国患者NK/TL中EB病毒潜伏膜蛋白1(LMP1)基因序列。在用基于左旋门冬酰胺酶的方案治疗前,通过桑格技术对13例患者血液中的病毒LMP1的6个克隆进行了测序,其中8例患者在整个治疗过程中都进行了测序。将21例无任何已知恶性肿瘤患者的血液LMP1序列作为对照进行检测。11/13例患者及所有对照均鉴定为EBV A型。治疗前,46.1%的NK/TL中发现含有30 bp缺失(del30)的克隆性LMP1基因,而对照中仅为4.8%。这些患者的治疗效果较差,死亡速度比其他患者更快。治疗期间缺失株向野生型株演变的患者达到完全缓解。通过高灵敏度的下一代测序技术对5例NK/TL鼻咽活检组织中的LMP1基因进行了测序,其中2例来自之前的患者。100% 的活检组织中存在del30;在3例活检组织中至少共存两种病毒。这些结果表明,del30可能与预后不良的NK/TL相关,并且毒株演变可作为监测治疗的潜在标志物。

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