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通过遗传编程生成稳定的单克隆抗体产生的 B 细胞受体阳性人类记忆 B 细胞。

Generation of stable monoclonal antibody-producing B cell receptor-positive human memory B cells by genetic programming.

机构信息

AIMM Therapeutics, Academic Medical Center, Amsterdam, The Netherlands.

出版信息

Nat Med. 2010 Jan;16(1):123-8. doi: 10.1038/nm.2071. Epub 2009 Dec 20.

Abstract

The B cell lymphoma-6 (Bcl-6) and Bcl-xL proteins are expressed in germinal center B cells and enable them to endure the proliferative and mutagenic environment of the germinal center. By introducing these genes into peripheral blood memory B cells and culturing these cells with two factors produced by follicular helper T cells, CD40 ligand (CD40L) and interleukin-21 (IL-21), we convert them to highly proliferating, cell surface B cell receptor (BCR)-positive, immunoglobulin-secreting B cells with features of germinal center B cells, including expression of activation-induced cytidine deaminase (AID). We generated cloned lines of B cells specific for respiratory syncytial virus and used these cells as a source of antibodies that effectively neutralized this virus in vivo. This method provides a new tool to study B cell biology and signal transduction through antigen-specific B cell receptors and for the rapid generation of high-affinity human monoclonal antibodies.

摘要

B 细胞淋巴瘤-6(Bcl-6)和 Bcl-xL 蛋白在生发中心 B 细胞中表达,使它们能够耐受生发中心的增殖和诱变环境。通过将这些基因引入外周血记忆 B 细胞,并与滤泡辅助 T 细胞产生的两种因子(CD40 配体[CD40L]和白细胞介素-21[IL-21])一起培养这些细胞,我们将其转化为高增殖、细胞膜 B 细胞受体(BCR)阳性、分泌免疫球蛋白的 B 细胞,具有生发中心 B 细胞的特征,包括激活诱导胞苷脱氨酶(AID)的表达。我们生成了针对呼吸道合胞病毒的特异性 B 细胞克隆系,并将这些细胞用作体内有效中和该病毒的抗体的来源。这种方法为通过抗原特异性 B 细胞受体研究 B 细胞生物学和信号转导以及快速产生高亲和力人单克隆抗体提供了一种新工具。

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