In vitro polyclonal activation of conventional T cells with a CD28 superagonist protects mice from acute graft versus host disease

被引:8
作者
Beyersdorf, Niklas [1 ]
Werner, Sandra [1 ]
Wolf, Nelli [1 ]
Huenig, Thomas [1 ]
Kerkau, Thomas [1 ]
机构
[1] Univ Wurzburg, Inst Virol & Immunobiol, D-97078 Wurzburg, Germany
关键词
aGvHD; Conventional T cells; CD28; superagonist; GvT effect; BONE-MARROW-TRANSPLANTATION; TUMOR VACCINE EFFICACY; EX-VIVO; PHASE-1; TRIAL; EXPANSION; LYMPHOCYTES; INDUCTION; PRESERVE; LEUKEMIA; MODEL;
D O I
10.1002/eji.201445317
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Upon transplantation of T cells from a CD28 superagonist (CD28-SA) treated donor into an irradiated allogeneic host, the CD28-SA-induced activation and expansion of T-reg cells inhibits acute graft versus host disease (aGvHD), while not abrogating the desired graft versus tumor effect. Human peripheral blood CD4(+) T cells, however, harbor only very few T-reg cells. Therefore, we studied whether polyclonal in vitro prestimulation of conventional, that is T-reg-cell-depleted, CD4(+) T cells of C57BL/6 mice with CD28-SA-coated paramagnetic beads is sufficient to protect recipient BALB/c mice from aGvHD. CD28-SA prestimulation of conventional CD4(+) T cells efficiently protected BALB/c recipient mice from aGvHD and CD28-SA-stimulated CD4(+) and CD8(+) T cells were capable of mediating long-term protection from the BCL1 lymphoma. The recently completed successful phase I testing of the human CD28-SA TGN1412/TAB08 should greatly facilitate further development of this straightforward method into a novel immunotherapy for patients.
引用
收藏
页码:1997 / 2007
页数:11
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