离体
移植物抗宿主病
白细胞介素2受体
白细胞介素-7受体
免疫学
免疫抑制
医学
体内
疾病
生物
T细胞
免疫系统
内科学
生物技术
作者
Piotr Trzonkowski,Maria Bieniaszewska,Jolanta Juścińska,Anita Dobyszuk,Adam Krzystyniak,Natalia Marek-Trzonkowska,Jolanta Myśliwska,Andrzej Hellmann
标识
DOI:10.1016/j.clim.2009.06.001
摘要
Here, we describe a procedure and first-in-man clinical effects of adoptive transfer of ex vivo expanded CD4+CD25+CD127− T regulatory cells (Tregs) in the treatment of graft versus host disease (GvHD). The cells were sorted from buffy coats taken from two family donors, expanded ex vivo and transferred to respective recipients who suffered from either acute or chronic GvHD. The therapy allowed for significant alleviation of the symptoms and reduction of pharmacologic immunosuppression in the case of chronic GvHD, while in the case of grade IV acute GvHD it only transiently improved the condition, for the longest time within all immunosuppressants used nonetheless.
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