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本文引用的文献

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Activation of mouse complement by monoclonal mouse antibodies.单克隆小鼠抗体对小鼠补体的激活作用。
Eur J Immunol. 1981 Dec;11(12):1012-6. doi: 10.1002/eji.1830111212.
2
Preparation of monoclonal antibodies: strategies and procedures.单克隆抗体的制备:策略与程序
Methods Enzymol. 1981;73(Pt B):3-46. doi: 10.1016/0076-6879(81)73054-4.
3
Arrangement of human immunoglobulin heavy chain constant region genes implies evolutionary duplication of a segment containing gamma, epsilon and alpha genes.人类免疫球蛋白重链恒定区基因的排列意味着包含γ、ε和α基因的片段发生了进化性重复。
Nature. 1982 Dec 23;300(5894):709-13. doi: 10.1038/300709a0.
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Structure of human immunoglobulin gamma genes: implications for evolution of a gene family.人类免疫球蛋白γ基因的结构:对一个基因家族进化的启示
Cell. 1982 Jun;29(2):671-9. doi: 10.1016/0092-8674(82)90183-0.
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Regulation of the antibody response against hapten-coupled erythrocytes by monoclonal antihapten antibodies of various isotypes.不同同种型的单克隆抗半抗原抗体对针对半抗原偶联红细胞的抗体反应的调节。
Cell Immunol. 1982 Aug;71(2):365-73. doi: 10.1016/0008-8749(82)90270-2.
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Enhancer-dependent expression of human kappa immunoglobulin genes introduced into mouse pre-B lymphocytes by electroporation.通过电穿孔导入小鼠前B淋巴细胞的人κ免疫球蛋白基因的增强子依赖性表达。
Proc Natl Acad Sci U S A. 1984 Nov;81(22):7161-5. doi: 10.1073/pnas.81.22.7161.
7
Chimeric human antibody molecules: mouse antigen-binding domains with human constant region domains.嵌合人源抗体分子:具有人恒定区结构域的小鼠抗原结合结构域。
Proc Natl Acad Sci U S A. 1984 Nov;81(21):6851-5. doi: 10.1073/pnas.81.21.6851.
8
Mechanisms of divergence and convergence of the human immunoglobulin alpha 1 and alpha 2 constant region gene sequences.人类免疫球蛋白α1和α2恒定区基因序列的分化与趋同机制
Cell. 1984 Mar;36(3):681-8. doi: 10.1016/0092-8674(84)90348-9.
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Immunoglobulin gene expression in transformed lymphoid cells.转化淋巴细胞中的免疫球蛋白基因表达。
Proc Natl Acad Sci U S A. 1983 Feb;80(3):825-9. doi: 10.1073/pnas.80.3.825.
10
Removal of T cells from bone marrow for transplantation: a monoclonal antilymphocyte antibody that fixes human complement.从骨髓中去除T细胞用于移植:一种能固定人补体的单克隆抗淋巴细胞抗体。
Blood. 1983 Oct;62(4):873-82.

使用一组匹配的嵌合抗体比较人免疫球蛋白的效应器功能。

Comparison of the effector functions of human immunoglobulins using a matched set of chimeric antibodies.

作者信息

Brüggemann M, Williams G T, Bindon C I, Clark M R, Walker M R, Jefferis R, Waldmann H, Neuberger M S

机构信息

Department of Pathology, Addenbrooke's Hospital, Cambridge, United Kingdom.

出版信息

J Exp Med. 1987 Nov 1;166(5):1351-61. doi: 10.1084/jem.166.5.1351.

DOI:10.1084/jem.166.5.1351
PMID:3500259
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2189658/
Abstract

Cell lines have been established that secrete a matched set of human chimeric IgM, IgG1, IgG2, IgG3, IgG4, IgE, and IgA2 antibodies that are directed against the hapten 4-hydroxy-3-nitrophenacetyl. These chimeric antibodies secreted from mouse plasmacytoma cells behave exactly like their authentic human counterparts in SDS-PAGE analysis, binding to protein A and in a wide range of serological assays. The antibodies have been compared in their ability to bind human C1q as well as in their efficacy in mediating lysis of human erythrocytes in the presence of human complement. A major conclusion to emerge is that whereas IgG3 bound C1q better than did IgG1, the chimeric IgG1 was much more effective than all the other IgG subclasses in complement-dependent hemolysis. The IgG1 antibody was also the most effective in mediating antibody-dependent cell-mediated cytotoxicity using both human effector and human target cells. These results suggest that IgG1 might be the favoured IgG subclass for therapeutic applications.

摘要

已经建立了一些细胞系,它们能分泌一组匹配的人源嵌合IgM、IgG1、IgG2、IgG3、IgG4、IgE和IgA2抗体,这些抗体针对半抗原4-羟基-3-硝基苯乙酰。从小鼠浆细胞瘤细胞分泌的这些嵌合抗体在SDS-PAGE分析、与蛋白A结合以及广泛的血清学检测中,其行为与真正的人源对应抗体完全一样。对这些抗体结合人C1q的能力以及在存在人补体的情况下介导人红细胞裂解的效力进行了比较。得出的一个主要结论是,虽然IgG3比IgG1更能结合C1q,但嵌合IgG1在补体依赖性溶血方面比所有其他IgG亚类都更有效。在使用人效应细胞和人靶细胞介导抗体依赖性细胞介导的细胞毒性方面,IgG1抗体也是最有效的。这些结果表明,IgG1可能是治疗应用中最受青睐的IgG亚类。