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亲和力和独特型表位识别对大鼠单克隆抗独特型抗体调节人恶性B细胞表面免疫球蛋白的影响。

Influence of avidity and idiotope recognition on the modulation of surface immunoglobulin on malignant human B cells by rat monoclonal anti-idiotype antibodies.

作者信息

Campbell M, Bieber M, Levy R, Teng N N

出版信息

J Immunol. 1986 Apr 15;136(8):2983-8.

PMID:3485677
Abstract

Immunoglobulin (Ig) was obtained from the tumor cells of patients with B cell malignancies by somatic cell hybridization to mouse-human heteromyeloma cells. The human Ig secreted by one of these hybridomas was used as an immunogen for the production of rat monoclonal antibodies (mAb). A panel of mAb specific for the idiotype (Id) was produced and characterized. Competitive binding studies that made use of [Se]-labeled anti-Id mAb (MAID) demonstrated several distinct yet topographically related Id on the Id-bearing Ig. These antibodies were shown to have avidities ranging from 0.38 to 45.3 X 10(8) l/mol. Additional studies demonstrated varying degrees of antigenic modulation of surface Id in vitro by MAID. The degree of modulation correlates with antibody avidity.

摘要

通过将B细胞恶性肿瘤患者的肿瘤细胞与小鼠 - 人异源骨髓瘤细胞进行体细胞杂交获得免疫球蛋白(Ig)。其中一种杂交瘤分泌的人Ig被用作免疫原,用于制备大鼠单克隆抗体(mAb)。制备并鉴定了一组针对独特型(Id)的单克隆抗体。利用[Se]标记的抗独特型单克隆抗体(MAID)进行的竞争性结合研究表明,携带Id的Ig上存在几种不同但在拓扑结构上相关的Id。这些抗体的亲和力范围为0.38至45.3×10⁸ l/mol。进一步的研究表明,MAID在体外对表面Id具有不同程度的抗原调节作用。调节程度与抗体亲和力相关。

相似文献

1
Influence of avidity and idiotope recognition on the modulation of surface immunoglobulin on malignant human B cells by rat monoclonal anti-idiotype antibodies.亲和力和独特型表位识别对大鼠单克隆抗独特型抗体调节人恶性B细胞表面免疫球蛋白的影响。
J Immunol. 1986 Apr 15;136(8):2983-8.
2
Strategies for production of monoclonal anti-idiotype antibodies against human B cell lymphomas.针对人类B细胞淋巴瘤产生单克隆抗独特型抗体的策略。
J Immunol. 1984 Jul;133(1):495-501.
3
Idiotypic analysis of anti-I-Ak monoclonal antibodies. I. Production and characterization of syngeneic anti-idiotypic mAb against an anti-I-Ak mAb.抗I-Ak单克隆抗体的独特型分析。I. 针对一种抗I-Ak单克隆抗体的同基因抗独特型单克隆抗体的产生与特性鉴定
J Immunol. 1984 Nov;133(5):2587-94.
4
Expression of idiotype on the surface of human B cells producing anti-DNA antibody.产生抗DNA抗体的人B细胞表面独特型的表达。
J Immunol. 1986 Feb 15;136(4):1241-6.
5
Anti-idiotypic antibodies recognizing stable epitopes limit the emergence of idiotype variants in a murine B cell lymphoma.识别稳定表位的抗独特型抗体限制了小鼠B细胞淋巴瘤中独特型变体的出现。
J Immunol. 1990 Mar 15;144(6):2436-45.
6
Analysis of the interaction of antibodies with immunoglobulin idiotypes on neoplastic B lymphocytes: implications for immunotherapy.肿瘤性B淋巴细胞上抗体与免疫球蛋白独特型相互作用的分析:对免疫治疗的意义。
J Immunol. 1987 Feb 1;138(3):981-8.
7
Immunoglobulin-specific T-B cell interaction. IV. B cell presentation of idiotypic determinant(s) of monoclonal anti-surface immunoglobulin antibody to idiotope-recognizing helper T clones.免疫球蛋白特异性T-B细胞相互作用。IV. 单克隆抗表面免疫球蛋白抗体独特型决定簇向识别独特位的辅助性T细胞克隆的B细胞呈递。
Eur J Immunol. 1990 Aug;20(8):1691-6. doi: 10.1002/eji.1830200811.
8
Idiotope mapping on the variable region of an antibody clonotype produced by normal (nonmalignant) human B cells.对正常(非恶性)人类B细胞产生的抗体克隆型可变区进行独特型定位。
J Immunol. 1985 Dec;135(6):4066-72.
9
Idiotype variants emerging after anti-idiotype monoclonal antibody therapy of a murine B cell lymphoma.鼠源B细胞淋巴瘤经抗独特型单克隆抗体治疗后出现的独特型变体。
J Immunol. 1989 Jan 1;142(1):343-51.
10
Shared idiotope on monoclonal anti-Ia.7 antibodies reactive with determinants in a structural domain of the I-E molecules.与I-E分子结构域中的决定簇反应的单克隆抗Ia.7抗体上的共享独特型。
J Immunol. 1984 Mar;132(3):1353-60.

引用本文的文献

1
Antibody-induced modulation of CD26 surface expression.抗体诱导的CD26表面表达调节。
Immunology. 1995 Apr;84(4):595-600.
2
Construction of an extended three-dimensional idiotope map by electron microscopic analysis of idiotope-anti-idiotope complexes.通过对独特型-抗独特型复合物进行电子显微镜分析构建扩展的三维独特型图谱。
Proc Natl Acad Sci U S A. 1987 Jul;84(14):4984-8. doi: 10.1073/pnas.84.14.4984.
3
Dual conformations of an immunoglobulin light-chain dimer: heterogeneity of antigen specificity and idiotope profile may result from multiple variable-domain interaction mechanisms.
免疫球蛋白轻链二聚体的双重构象:抗原特异性和独特型谱的异质性可能源于多种可变结构域相互作用机制。
Proc Natl Acad Sci U S A. 1988 Sep;85(18):6895-9. doi: 10.1073/pnas.85.18.6895.