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原发性脑淋巴瘤中的免疫球蛋白重链重排。一项使用聚合酶链反应扩增互补决定区III的研究。

Immunoglobulin heavy chain rearrangements in primary brain lymphomas. A study using PCR to amplify CDR-III.

作者信息

Albrecht S, Bruner J M, Segall G K

机构信息

Department of Pathology, Baylor College of Medicine, Houston, Texas.

出版信息

J Pathol. 1993 Mar;169(3):297-302. doi: 10.1002/path.1711690304.

Abstract

Primary brain lymphomas (PBLs) have only rarely been analysed for immunoglobulin heavy chain (IgH) rearrangements. In this study, DNA was extracted from paraffin blocks in 23 cases of PBL and examined for IgH rearrangements using the polymerase chain reaction (PCR) to amplify the complementarity-determining region III (CDR-III) of rearranged IgH genes. Fifteen of the cases were phenotyped on paraffin-embedded tissue using a pan-B and pan-T antibody (L26 and UCHL-1, respectively). The remaining eight cases were not phenotyped for lack of tissue. For comparison, we used DNA extracted from paraffin blocks of normal brain, lymph nodes with lymphoid hyperplasia, and non-lymphoid malignancies. PCR products were examined by polyacrylamide gel electrophoresis. Among the ten B-cell PBL; four had a pattern indicative of IgH rearrangement, one had a germline pattern, and five had no detectable PCR products. Among the five T-cell PBLs, one had a germline pattern and four had no detectable products. Among the eight untyped PBLs, two had IgH rearrangement, four had a germline pattern, and two gave no detectable products. DNA from non-lymphoid tissues gave a consistent germline pattern, while DNA from polyclonal lymphoid populations (lymph node) had a pattern of polyclonal IgH rearrangement. In a dilution study, a clonal rearrangement could be detected as long as the clone's DNA constituted at least 10 per cent of the total DNA. PCR to amplify CDR-III can be successfully applied to DNA extracted from paraffin blocks, and it detected a clonal rearrangement in 50 per cent of cases that gave a detectable pattern.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

原发性脑淋巴瘤(PBLs)很少进行免疫球蛋白重链(IgH)重排分析。在本研究中,从23例PBL的石蜡块中提取DNA,使用聚合酶链反应(PCR)扩增重排IgH基因的互补决定区III(CDR-III),检测IgH重排。其中15例在石蜡包埋组织上使用泛B和泛T抗体(分别为L26和UCHL-1)进行表型分析。其余8例因缺乏组织未进行表型分析。为作比较,我们使用从正常脑、淋巴组织增生的淋巴结和非淋巴恶性肿瘤的石蜡块中提取的DNA。PCR产物通过聚丙烯酰胺凝胶电泳检测。在10例B细胞PBL中,4例有提示IgH重排的模式,1例为种系模式,5例未检测到PCR产物。在5例T细胞PBL中,1例为种系模式,4例未检测到产物。在8例未分型的PBL中,2例有IgH重排,4例为种系模式,2例未检测到产物。非淋巴组织的DNA呈现一致的种系模式,而多克隆淋巴群体(淋巴结)的DNA有多克隆IgH重排模式。在稀释研究中,只要克隆的DNA占总DNA的至少10%,就能检测到克隆重排。扩增CDR-III的PCR可成功应用于从石蜡块中提取的DNA,在50%能检测到模式的病例中检测到了克隆重排。(摘要截短至250字)

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