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急性爱泼斯坦-巴尔病毒所致传染性单核细胞增多症患者血液淋巴细胞中的寡克隆性T细胞受体基因重排

Oligoclonal T cell receptor gene rearrangements in blood lymphocytes of patients with acute Epstein-Barr virus-induced infectious mononucleosis.

作者信息

Strickler J G, Movahed L A, Gajl-Peczalska K J, Horwitz C A, Brunning R D, Weiss L M

机构信息

Department of Pathology, University of Minnesota Hospital, Minneapolis 55455.

出版信息

J Clin Invest. 1990 Oct;86(4):1358-63. doi: 10.1172/JCI114847.

Abstract

Gene rearrangement studies were performed on blood lymphocytes from eight patients with acute Epstein-Barr virus-induced infectious mononucleosis. The diagnosis in each case was based on characteristic clinical, hematologic, and serologic findings. The blood lymphocytes in each patient consisted predominantly of CD8+ T cells. EBV DNA was detected in seven patients by Southern blot analysis (EBV Bam HI W probe, Bam HI). A germline configuration was found for the immunoglobulin heavy and light chain genes (JH probe, Bam HI and Eco RI; C kappa probe, Bam HI; and C lambda probe, Eco RI). T cell receptor gene rearrangements were detected with J gamma and J beta 1 + 2 probes. Using a J gamma probe with two different restriction enzymes (Bgl II and Eco RI), the blood from each patient showed several bands corresponding to the polyclonal pattern previously described in the blood of normal individuals. Using J beta 1 + 2 probes with two different restriction enzymes (Bgl II and Bam HI), each case showed from 3 to about 12 extragermline bands of varying intensity and in different locations from case to case. In addition, each case showed relative deletion of the J beta 1 germline band. This oligoclonal pattern of T cell receptor gene rearrangements has not been previously reported in benign or malignant T cell populations.

摘要

对8例急性爱泼斯坦-巴尔病毒引起的传染性单核细胞增多症患者的血液淋巴细胞进行了基因重排研究。每例患者的诊断均基于特征性的临床、血液学和血清学检查结果。每位患者的血液淋巴细胞主要由CD8 + T细胞组成。通过Southern印迹分析(EBV Bam HI W探针,Bam HI)在7例患者中检测到EBV DNA。免疫球蛋白重链和轻链基因(JH探针,Bam HI和Eco RI;Cκ探针,Bam HI;以及Cλ探针,Eco RI)呈现种系构型。用Jγ和Jβ1 + 2探针检测到T细胞受体基因重排。使用带有两种不同限制酶(Bgl II和Eco RI)的Jγ探针,每位患者的血液均显示出几条与正常个体血液中先前描述的多克隆模式相对应的条带。使用带有两种不同限制酶(Bgl II和Bam HI)的Jβ1 + 2探针,每例均显示出3至约12条种系外条带,强度各异且位置因病例而异。此外,每例均显示Jβ1种系条带相对缺失。这种T细胞受体基因重排的寡克隆模式在良性或恶性T细胞群体中此前尚未见报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e935/296871/0f1ea5f4c915/jcinvest00076-0352-a.jpg

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