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Antigen-specific human T-cell responses and T cell–dependent production of human antibodies in a humanized mouse model

机译:在人源化小鼠模型中抗原特异性的人类T细胞反应和人类抗体的T细胞依赖性产生

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摘要

Humanized mice with a functional human immune system would be very useful for in vivo studies of human immunobiology. We have previously shown that cotransplantation of human fetal thymus/liver tissues and CD34+ fetal liver cells into immunodeficient nonobese diabetic severe combined immunodeficiency (NOD/SCID) mice leads to the development of multiple lineages of human lymphohematopoietic cells and formation of secondary lymphoid organs with normal architecture. Here, we evaluated the ability of these humanized mice to develop antigen-specific, T cell–dependent antibody responses after in vivo immunization with T-dependent antigen, 2,4-dinitrophenyl hapten-keyhole limpet hemocyanin (DNP23-KLH). Human T cells from DNP23-KLH–immunized mice showed strong proliferation in response to KLH in vitro. Furthermore, T cell–dependent production of DNP-specific human antibodies (mainly IgG1 and IgG2) was detected in all immunized mice. These results confirm that a functional human immune system can be established in immunodeficient mice through cotransplantation of human fetal thymus/liver tissues and CD34+ hematopoietic stem/progenitor cells.
机译:具有人体免疫系统功能的人源化小鼠对于人体免疫生物学的体内研究非常有用。先前我们已经表明,将人胎胸腺/肝组织和CD34 +胎肝细胞共移植到免疫缺陷性非肥胖糖尿病严重合并免疫缺陷症(NOD / SCID)小鼠中会导致人淋巴造血细胞多种谱系的发育并形成正常的继发性淋巴器官建筑。在这里,我们评估了这些人源化小鼠体内用T依赖性抗原2,4-二硝基苯基半抗原-匙孔戚血蓝蛋白(DNP23-KLH)免疫后产生抗原特异性,T细胞依赖性抗体反应的能力。来自DNP23-KLH免疫小鼠的人类T细胞在体外对KLH表现出强烈的增殖。此外,在所有免疫小鼠中都检测到了T细胞依赖性DNP特异性人类抗体(主要是IgG1和IgG2)的产生。这些结果证实,可以通过人胚胎胸腺/肝组织和CD34 +造血干细胞/祖细胞的共移植,在免疫缺陷小鼠中建立功能性的人免疫系统。

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