Suppr超能文献

来自91例患者的伯基特淋巴瘤活检细胞上的表面免疫球蛋白

Surface immunoglobulins on Burkitt's lymphoma biopsy cells from 91 patients.

作者信息

Gunvén P, Klein G, Klein E, Norin T, Singh S

机构信息

Department of Tumor Biology, Karolinska Institutet, S-104 01 Stockholm, Sweden.

出版信息

Int J Cancer. 1980 Jun 15;25(6):711-9. doi: 10.1002/ijc.2910250605.

Abstract

One hundred and fourteen biopsies from 91 cases of African Burkitt's lymphoma were examined by immunofluorescence methods for the presence of surface-associated mu, gamma, delta, kappa and lambda chains, as well as for the Fc region of gamma chains and for beta1C. Only 5% of the biopsies were surface-Ig-negative; 18% were negative for mu chains and 61% for gamma chains. Delta chain staining was absent, or borderline in a few tumors. Mu chains, gamma chains in a few highly reactive tumors and, in many cases, the predominant light chain seemed to be clonal markers. They gave no convincing evidence of more than one cell clone, either within single tumors or within syn- or metachronous tumors in one individual. Gamma chains in moderately stained tumors, Fc and beta1C correlated with each other and the first two reactivities decreased after incubation at low pH, indicating that their presence resulted from outside coating of the cells. The results indicated that one clone of B cells is involved in Burkitt's lymphoma in the large majority of cases. This clone is in a state of differentiation at which surface delta chains are not expressed. No prognostic information resulted from the analysis of the markers studied.

摘要

采用免疫荧光法对91例非洲伯基特淋巴瘤患者的114份活检标本进行检测,以确定其表面相关的μ、γ、δ、κ和λ链的存在情况,以及γ链的Fc区和β1C的情况。仅5%的活检标本表面免疫球蛋白呈阴性;18%的标本μ链呈阴性,61%的标本γ链呈阴性。少数肿瘤未检测到δ链染色,或呈临界状态。μ链、少数高反应性肿瘤中的γ链以及在许多情况下,优势轻链似乎是克隆标志物。无论是在单个肿瘤内还是在同一个体的同步或异时肿瘤内,均未提供令人信服的证据表明存在多个细胞克隆。中度染色肿瘤中的γ链、Fc和β1C相互关联,前两种反应性在低pH孵育后降低,表明它们的存在是由于细胞外包裹所致。结果表明,在大多数情况下,伯基特淋巴瘤涉及一个B细胞克隆。该克隆处于不表达表面δ链的分化状态。对所研究标志物的分析未得出预后信息。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验