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慢性淋巴细胞白血病中一个保守的κ轻链可变区基因的高频表达

High-frequency expression of a conserved kappa light-chain variable-region gene in chronic lymphocytic leukemia.

作者信息

Kipps T J, Fong S, Tomhave E, Chen P P, Goldfien R D, Carson D A

出版信息

Proc Natl Acad Sci U S A. 1987 May;84(9):2916-20. doi: 10.1073/pnas.84.9.2916.

Abstract

Malignant B lymphocytes from several patients with chronic lymphocytic leukemia (CLL) were examined for reactivity with murine monoclonal antibody 17.109. This antibody, prepared against the rheumatoid factor (RF) paraprotein Sie, recognizes a crossreactive idiotype on 48% of human IgM RF paraproteins, but does not react with IgM paraproteins without RF activity or substantially with normal pooled immunoglobulin. The 17.109-reactive idiotype is a marker for a kappa III variable-region gene, designated V kappa RF, that is conserved in outbred human populations. In a limited study of 31 CLL patients, the leukemic cells from 5 of 20 patients with kappa light chain-expressing CLL were recognized by the 17.109 monoclonal antibody. Despite having malignant cells specifically reactive with this antibody, patients with 17.109-positive CLL did not have elevated serum levels of circulating antibody bearing 17.109-reactive determinants. Total RNAs isolated from the CLL B lymphocytes, or from hybridomas produced by fusing the CLL cells with the WI-L2-729-HF2 cell line, were fractionated electrophoretically and examined by blot hybridization. Under stringent hybridization conditions capable of discerning a single base-pair mismatch, RNA from the 17.109-idiotype-positive CLL cells hybridized to synthetic oligonucleotide probes corresponding to framework and complementary-determining regions in the V kappa RF gene. The high frequency of the 17.109-associated idiotype and the V kappa RF gene in CLL suggests that the disease may arise from B lymphocytes that express a restricted set of inherited immunoglobulin variable-region genes with little or no somatic mutation.

摘要

对多名慢性淋巴细胞白血病(CLL)患者的恶性B淋巴细胞进行检测,观察其与鼠单克隆抗体17.109的反应性。该抗体是针对类风湿因子(RF)副蛋白Sie制备的,可识别48%的人IgM RF副蛋白上的交叉反应独特型,但不与无RF活性的IgM副蛋白反应,也基本不与正常混合免疫球蛋白反应。17.109反应性独特型是κIII可变区基因(命名为VκRF)的标志物,该基因在远交人群中保守。在对31例CLL患者的有限研究中,20例表达κ轻链的CLL患者中有5例的白血病细胞可被17.109单克隆抗体识别。尽管17.109阳性CLL患者的恶性细胞与该抗体有特异性反应,但这些患者血清中携带17.109反应性决定簇的循环抗体水平并未升高。从CLL B淋巴细胞或通过将CLL细胞与WI-L2-729-HF2细胞系融合产生的杂交瘤中分离的总RNA进行电泳分级分离,并通过印迹杂交检测。在能够辨别单个碱基对错配的严格杂交条件下,17.109独特型阳性CLL细胞的RNA与对应于VκRF基因框架区和互补决定区的合成寡核苷酸探针杂交。CLL中17.109相关独特型和VκRF基因的高频率表明,该疾病可能源于表达一组有限的遗传性免疫球蛋白可变区基因且几乎没有或没有体细胞突变的B淋巴细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e346/304771/d56c1a73d380/pnas00274-0365-a.jpg

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