Takayama T, Morelli A E, Robbins P D, Tahara H, Thomson A W
Thomas E Starzl Transplantation Institute, University of Pittsburgh Medical Center, PA 15213, USA.
Gene Ther. 2000 Aug;7(15):1265-73. doi: 10.1038/sj.gt.3301244.
Dendritic cells (DC) are highly specialised, bone marrow (BM)-derived antigen-presenting cells (APC) that initiate and regulate immune responses. They provide costimulatory signals (in particular, CD40 and the CD28 ligands CD80 and CD86) necessary for naive T cell activation. Functional expression of CD80 and CD86 is blocked by the fusion protein cytotoxic T lymphocyte antigen 4-immunoglobulin (CTLA4Ig), that promotes tolerance induction in animals. Here, replicating mouse (B10; H2b) myeloid DC progenitors, were retrovirally transduced to express CTLA4Ig using the centrifugal enhancement method. Gene product was detected by immunocyto- or histochemistry. Maximal DC transduction efficiency was 62%. Compared with control, zeomycin-resistance gene (Zeo)-transduced DC, CTLA4Ig-expressing cells showed markedly impaired capacity to stimulate naive allogeneic (C3H; H2k) T cell proliferation and cytotoxic T lymphocyte (CTL) generation. Their ability to induce alloantigen-specific T cell hyporesponsiveness was reversed by exogenous IL-2 in secondary mixed leukocyte reactions (MLR). Following local (s.c.) transfer to allogeneic recipients, the genetically modified DC trafficked to T cell areas of draining lymphoid tissue, where transgene expression was detected. Ex vivo analysis of proliferative and CTL responses revealed donor-specific inhibition of alloimmune reactivity by the CTLA4Ig-transduced DC. This effect was associated with marked inhibition of interferon (IFN)-gamma production, but significant augmentation of IL-4 and IL-10 secretion. Thus, retroviral transduction of DC permits in vivo delivery of CTLA4Ig to the precise microenvironment where antigen (Ag) presentation occurs. Comparatively nonimmunogenic retroviral vectors, that allow permanent transgene expression in DC, and promote localized delivery of the immunosuppressive transgene product, promote immune deviation and Ag-specific T cell hyporesponsiveness.
树突状细胞(DC)是高度特化的、源自骨髓(BM)的抗原呈递细胞(APC),可启动并调节免疫反应。它们提供幼稚T细胞活化所需的共刺激信号(特别是CD40以及CD28配体CD80和CD86)。CD80和CD86的功能性表达被融合蛋白细胞毒性T淋巴细胞抗原4-免疫球蛋白(CTLA4Ig)阻断,CTLA4Ig可促进动物体内的耐受性诱导。在此,使用离心增强法通过逆转录病毒转导复制型小鼠(B10;H2b)髓样DC祖细胞以表达CTLA4Ig。通过免疫细胞化学或组织化学检测基因产物。最大DC转导效率为62%。与对照的、转导了博来霉素抗性基因(Zeo)的DC相比,表达CTLA4Ig的细胞刺激幼稚同种异体(C3H;H2k)T细胞增殖和细胞毒性T淋巴细胞(CTL)生成的能力明显受损。在二次混合淋巴细胞反应(MLR)中,外源性IL-2可逆转它们诱导同种抗原特异性T细胞低反应性的能力。将其局部(皮下)转移至同种异体受体后,转基因DC迁移至引流淋巴组织的T细胞区域,并在该区域检测到转基因表达。对增殖反应和CTL反应的体外分析显示,转导了CTLA4Ig的DC对同种免疫反应具有供体特异性抑制作用。这种作用与干扰素(IFN)-γ产生的显著抑制相关,但IL-4和IL-10分泌显著增加。因此,DC的逆转录病毒转导可将CTLA4Ig体内递送至发生抗原(Ag)呈递的精确微环境。相对无免疫原性的逆转录病毒载体可使DC中实现转基因的永久表达,并促进免疫抑制转基因产物的局部递送,从而促进免疫偏离和Ag特异性T细胞低反应性。