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对一名患有慢性淋巴细胞白血病和大细胞淋巴瘤(里氏综合征)患者的抗独特型抗体分析。

Analysis with antiidiotype antibody of a patient with chronic lymphocytic leukemia and a large cell lymphoma (Richter's syndrome).

作者信息

Bertoli L F, Kubagawa H, Borzillo G V, Mayumi M, Prchal J T, Kearney J F, Durant J R, Cooper M D

出版信息

Blood. 1987 Jul;70(1):45-50.

PMID:3297206
Abstract

A murine monoclonal antibody made against an idiotypic determinant (Id) of surface IgM/IgD lambda molecules on chronic lymphocytic leukemia (CLL) cells of a 71-year-old woman was used for clonal analysis by two-color immunofluorescence. The anti-Id antibody identified IgM+/IgD+/lambda+ B cells as the predominant cell type of her CLL clone. In addition, substantial proportions of the IgG and IgA B cells and most of the IgM plasma cells in her bone marrow and blood were Id+. Six years after diagnosis, the patient died of respiratory failure due to infiltration of lungs by malignant cells. Autopsy revealed a dramatic change in the tumor cell morphology. The lungs, hilar nodes, and liver were infiltrated by a diffuse large cell lymphoma admixed with the leukemic cells. By immunohistologic staining these anaplastic lymphoma cells were IgM+/IgD-/lambda+ B cells expressing the same Id noted earlier on the CLL cells. The immunoglobulin gene rearrangement pattern on Southern blot analysis was also the same in leukemic blood cells and in the tissues involved by the lymphoma. Thus, the combination of antiidiotype and immunoglobulin gene analyses in this patient with Richter's syndrome revealed that a CLL clone, seemingly "frozen" in differentiation, was actually undergoing isotype switching, differentiation into plasma cells, and evolution into a rapidly growing and fetal lymphoma.

摘要

用针对一名71岁女性慢性淋巴细胞白血病(CLL)细胞表面IgM/IgD λ分子的独特型决定簇(Id)制备的鼠单克隆抗体,通过双色免疫荧光进行克隆分析。抗Id抗体将IgM+/IgD+/λ+ B细胞鉴定为她的CLL克隆的主要细胞类型。此外,她骨髓和血液中相当比例的IgG和IgA B细胞以及大多数IgM浆细胞都是Id阳性。诊断6年后,患者死于恶性细胞浸润肺部导致的呼吸衰竭。尸检显示肿瘤细胞形态发生了显著变化。肺、肺门淋巴结和肝脏被弥漫性大细胞淋巴瘤浸润,其中混有白血病细胞。通过免疫组织化学染色,这些间变性淋巴瘤细胞是IgM+/IgD-/λ+ B细胞,表达与早期CLL细胞相同的Id。Southern印迹分析显示白血病血细胞和淋巴瘤累及组织中的免疫球蛋白基因重排模式也相同。因此,对该Richter综合征患者进行抗独特型和免疫球蛋白基因分析表明,一个看似在分化中“停滞”的CLL克隆实际上正在进行同种型转换、分化为浆细胞,并演变成快速生长的侵袭性淋巴瘤。

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