Brown M P, Topham D J, Sangster M Y, Zhao J, Flynn K J, Surman S L, Woodland D L, Doherty P C, Farr A G, Pattengale P K, Brenner M K
Cell and Gene Therapy Program, St Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.
Nat Med. 1998 Nov;4(11):1253-60. doi: 10.1038/3233.
Inherited deficiency of the CD40 ligand (X-linked hyper-IgM syndrome) is characterized by failure of immunoglobulin isotype switching and severe defects of cell-mediated immunity. To test the potential for gene transfer therapy to correct this disorder, we transduced murine bone marrow or thymic cells with a retroviral vector containing the cDNA for the murine CD40 ligand (CD40L) and injected them into CD40L-/- mice. Even low-level, constitutive expression of the transgene stimulated humoral and cellular immune functions in these mice. With extended follow-up, however, 12 of 19 treated mice developed T-lymphoproliferative disorders, ranging from polyclonal increases of lymphoblasts to overt monoclonal T-lymphoblastic lymphomas that involved multiple organs. Our findings show that constitutive (rather than tightly regulated), low-level expression of CD40L can produce abnormal proliferative responses in developing T lymphocytes, apparently through aberrant interaction between CD40L+ and TCRalphabeta+CD40+ thymocytes. Current methods of gene therapy may prove inappropriate for disorders involving highly regulated genes in essential positions in proliferative cascades.
CD40配体的遗传性缺陷(X连锁高IgM综合征)的特征是免疫球蛋白同种型转换失败和细胞介导的免疫严重缺陷。为了测试基因转移疗法纠正这种疾病的潜力,我们用含有小鼠CD40配体(CD40L)cDNA的逆转录病毒载体转导小鼠骨髓或胸腺细胞,并将其注入CD40L-/-小鼠体内。即使转基因的低水平组成型表达也能刺激这些小鼠的体液和细胞免疫功能。然而,随着随访时间的延长,19只接受治疗的小鼠中有12只出现了T淋巴细胞增殖性疾病,范围从淋巴母细胞的多克隆增加到涉及多个器官的明显单克隆T淋巴细胞淋巴瘤。我们的研究结果表明,CD40L的组成型(而非严格调控的)低水平表达可在发育中的T淋巴细胞中产生异常增殖反应,显然是通过CD40L+与TCRαβ+CD40+胸腺细胞之间的异常相互作用。目前的基因治疗方法可能不适用于涉及增殖级联反应中关键位置高度调控基因的疾病。