Transplantation Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02129, USA.
J Immunol Methods. 2013 May 31;391(1-2):103-11. doi: 10.1016/j.jim.2013.02.015. Epub 2013 Mar 5.
Targeted cell therapies are possible through the generation of recombinant fusion proteins that combine a toxin, such as diphtheria toxin (DT), with an antibody or other molecule that confers specificity. Upon binding of the fusion protein to the cell of interest, the diphtheria toxin is internalized which results in protein synthesis inhibition and subsequent cell death. We have recently expressed and purified the recombinant soluble porcine CTLA-4 both with and without N-glycosylation in yeast Pichia pastoris for in vivo use in our preclinical swine model. The glycosylated and non-N-glycosylated versions of this recombinant protein each bind to a porcine CD80 expressing B-cell lymphoma line (LCL13271) with equal affinity (K(D)=13 nM). In this study we have linked each of the glycosylated and non-N-glycosylated soluble porcine CTLA-4 proteins to the truncated diphtheria toxin DT390 through genetic engineering yielding three versions of the porcine CTLA-4 fusion toxins: 1) monovalent glycosylated soluble porcine CTLA-4 fusion toxin; 2) monovalent non-N-glycosylated soluble porcine CTLA-4 fusion toxin and 3) bivalent non-N-glycosylated soluble porcine CTLA-4 fusion toxin. Protein synthesis inhibition analysis demonstrated that while all three fusion toxins are capable of inhibiting protein synthesis in vitro, the non-N-glycosylated porcine CTLA-4 isoforms function most efficiently. Binding analysis using flow cytometry of the porcine CTLA-4 fusion toxins to LCL13271 cells also demonstrated that the non-N-glycosylated porcine CTLA-4 isoforms bind to these cells with higher affinity compared to the glycosylated fusion toxin. The monovalent non-N-glycosylated porcine CTLA-4 fusion toxin was tested in vivo. NSG (NOD/SCID IL-2 receptor γ(-)/(-)) mice were injected with porcine CD80(+) LCL13271 tumor cells. All animals succumbed to tumors and those treated with the monovalent non-N-glycosylated porcine CTLA-4 fusion toxin survived longer based on a symptomatic scoring system compared to the untreated controls. This recombinant protein may therefore provide a novel approach for in vivo depletion of porcine antigen presenting cells (APCs) for studies investigating the induction of transplantation tolerance, autoimmune disease and cancer treatment.
靶向细胞疗法是通过生成重组融合蛋白来实现的,这些融合蛋白将毒素(如白喉毒素 (DT))与抗体或其他赋予特异性的分子结合。当融合蛋白与靶细胞结合时,白喉毒素被内化,导致蛋白质合成抑制和随后的细胞死亡。我们最近在毕赤酵母中表达和纯化了具有和不具有 N-糖基化的重组可溶性猪 CTLA-4,用于我们的临床前猪模型中的体内使用。该重组蛋白的糖基化和非 N-糖基化版本都以相等的亲和力(K(D)=13 nM)结合表达猪 CD80 的 B 细胞淋巴瘤系 (LCL13271)。在这项研究中,我们通过基因工程将每个糖基化和非 N-糖基化的可溶性猪 CTLA-4 蛋白与截短的白喉毒素 DT390 连接,得到了三种猪 CTLA-4 融合毒素:1)单价糖基化可溶性猪 CTLA-4 融合毒素;2)单价非 N-糖基化可溶性猪 CTLA-4 融合毒素和 3)二价非 N-糖基化可溶性猪 CTLA-4 融合毒素。蛋白质合成抑制分析表明,虽然所有三种融合毒素都能够在体外抑制蛋白质合成,但非 N-糖基化的猪 CTLA-4 同工型的作用效率最高。使用流式细胞术分析猪 CTLA-4 融合毒素与 LCL13271 细胞的结合也表明,与糖基化融合毒素相比,非 N-糖基化的猪 CTLA-4 同工型与这些细胞的结合具有更高的亲和力。单价非 N-糖基化的猪 CTLA-4 融合毒素在体内进行了测试。NSG(NOD/SCID IL-2 受体 γ(-)/(-))小鼠注射了猪 CD80(+) LCL13271 肿瘤细胞。所有动物都因肿瘤而死亡,与未治疗的对照组相比,用单价非 N-糖基化的猪 CTLA-4 融合毒素治疗的动物根据症状评分系统存活时间更长。因此,这种重组蛋白可能为体内耗尽猪抗原呈递细胞 (APC) 提供一种新方法,用于研究诱导移植耐受、自身免疫性疾病和癌症治疗。