Traggiai Elisabetta, Chicha Laurie, Mazzucchelli Luca, Bronz Lucio, Piffaretti Jean-Claude, Lanzavecchia Antonio, Manz Markus G
Institute for Research in Biomedicine (IRB), Via Vela 6, 6500 Bellinzona, Switzerland.
Science. 2004 Apr 2;304(5667):104-7. doi: 10.1126/science.1093933.
Because ethical restrictions limit in vivo studies of the human hemato-lymphoid system, substitute human to small animal xenotransplantation models have been employed. Existing models, however, sustain only limited development and maintenance of human lymphoid cells and rarely produce immune responses. Here we show that intrahepatic injection of CD34+ human cord blood cells into conditioned newborn Rag2-/-gammac-/- mice leads to de novo development of B, T, and dendritic cells; formation of structured primary and secondary lymphoid organs; and production of functional immune responses. This provides a valuable model to study development and function of the human adaptive immune system in vivo.
由于伦理限制阻碍了对人类血液淋巴系统的体内研究,因此采用了将人类细胞移植到小动物体内的异种移植模型。然而,现有的模型只能维持人类淋巴细胞的有限发育和维持,并且很少产生免疫反应。在这里,我们表明,将CD34+人类脐带血细胞肝内注射到经过预处理的新生Rag2-/-gammac-/-小鼠体内,会导致B细胞、T细胞和树突状细胞的从头发育;形成结构化的一级和二级淋巴器官;并产生功能性免疫反应。这为体内研究人类适应性免疫系统的发育和功能提供了一个有价值的模型。