Fu F, Li Y, Qian S, Lu L, Chambers F, Starzl T E, Fung J J, Thomson A W
Pittsburgh Transplantation Institute, University of Pittsburg, Pennsylvania 15213, USA.
Transplantation. 1996 Sep 15;62(5):659-65. doi: 10.1097/00007890-199609150-00021.
We have shown previously that granulocyte-macrophage colony-stimulating factor-stimulated mouse bone marrow-derived MHC class II+ dendritic cell (DC) progenitors that are deficient in cell surface expression of the costimulatory molecules B7-1 (CD80) and B7-2 (CD86) can induce alloantigen-specific T-cell anergy in vitro. To test the in vivo relevance of these findings, 2 x 10(6) B10 (H2b) mouse bone marrow-derived DC progenitors (NLDC 145+, MHC class II+, B7-1dim, B7-2-/dim) that induced T-cell hyporesponsiveness in vitro were injected systemically into normal C3H (H2k) recipients. Seven days later, the mice received heterotopic heart transplants from B10 donors. No immunosuppressive treatment was given. Median graft survival time was prolonged significantly from 9.5 to 22 days. Median graft survival time was also increased, although to a lesser extent (16.5 days), in mice that received third-party (BALB/c; H2d) DC progenitors. Ex vivo analysis of host T-cell responses to donor and third-party alloantigens 7 days after the injection of DC progenitors (the time of heart transplant) revealed minimal anti-donor mixed leukocyte reaction and cytotoxic T lymphocyte reactivity. These responses were reduced substantially compared with those of spleen cells from animals pretreated with "mature" granulocyte-macrophage colony-stimulating factor + interleukin-4-stimulated DC (MHC class IIbright, B7-1+, B7-2bright), many of which rejected their heart grafts in an accelerated fashion. Among the injected donor MHC class II+ DC progenitors that migrated to recipient secondary lymphoid tissue were cells that appeared to have up-regulated cell surface B7-1 and B7-2 molecule expression. This observation may explain, at least in part, the temporary or unstable nature of the hyporesponsiveness induced by the DC progenitors in nonimmunosuppressed recipients.
我们之前已经表明,粒细胞巨噬细胞集落刺激因子刺激的小鼠骨髓来源的MHC II类+树突状细胞(DC)祖细胞,其共刺激分子B7-1(CD80)和B7-2(CD86)的细胞表面表达缺陷,能够在体外诱导同种抗原特异性T细胞无反应性。为了测试这些发现的体内相关性,将2×10⁶个在体外诱导T细胞低反应性的B10(H2b)小鼠骨髓来源的DC祖细胞(NLDC 145⁺、MHC II类⁺、B7-1dim、B7-2⁻/dim)全身注射到正常C3H(H2k)受体中。7天后,这些小鼠接受来自B10供体的异位心脏移植。未给予免疫抑制治疗。中位移植物存活时间从9.5天显著延长至22天。在接受第三方(BALB/c;H2d)DC祖细胞的小鼠中,中位移植物存活时间也有所增加,尽管增加幅度较小(16.5天)。在注射DC祖细胞后7天(心脏移植时)对宿主T细胞对供体和第三方同种抗原的反应进行的体外分析显示,抗供体混合淋巴细胞反应和细胞毒性T淋巴细胞反应性极低。与用“成熟的”粒细胞巨噬细胞集落刺激因子+白细胞介素-4刺激的DC(MHC II类bright、B7-1⁺、B7-2bright)预处理的动物的脾细胞相比,这些反应显著降低,其中许多动物以加速方式排斥了它们的心脏移植物。在迁移到受体二级淋巴组织的注射供体MHC II类⁺DC祖细胞中,有一些细胞似乎上调了细胞表面B7-1和B7-2分子的表达。这一观察结果至少可以部分解释DC祖细胞在未免疫抑制的受体中诱导的低反应性的暂时或不稳定性质。