Park Julie R, Digiusto David L, Slovak Marilyn, Wright Christine, Naranjo Araceli, Wagner Jamie, Meechoovet Hunsar B, Bautista Cherrilyn, Chang Wen-Chung, Ostberg Julie R, Jensen Michael C
Department of Pediatric Hematology-Oncology, Children's Hospital and Medical Center, Seattle, Washington, USA.
Mol Ther. 2007 Apr;15(4):825-33. doi: 10.1038/sj.mt.6300104. Epub 2007 Feb 13.
Metastatic neuroblastoma is a poor-prognosis malignancy arising during childhood that overexpresses the L1-cell adhesion molecule (CD171). We have previously described a tumor L1-cell adhesion molecule-specific, single chain antibody-derived, chimeric antigen receptor designated CE7R for re-directing the antigen-specific effector functioning of cytolytic T lymphocytes. Here, we report on the feasibility of isolating, and the safety of infusing, autologous CD8(+) cytolytic T lymphocyte clones co-expressing CE7R and the selection-suicide expression enzyme HyTK in children with recurrent/refractory neuroblastoma. The cytolytic T lymphocyte products were derived from peripheral blood mononuclear cells that were subjected to polyclonal activation, plasmid vector electrotransfer, limiting dilution hygromycin selection, and expansion to numbers sufficient for adoptive transfer. In total, 12 infusions (nine at 10(8) cells/m(2), three at 10(9) cells/m(2)) were administered to six patients. No overt toxicities to tissues known to express L1-cell adhesion molecule (e.g., central nervous system, adrenal medulla, and sympathetic ganglia) were observed. The persistence of cytolytic T lymphocyte clones in the circulation, measured by vector-specific quantitative polymerase chain reaction, was short (1-7 days) in patients with bulky disease, but significantly longer (42 days) in a patient with a limited disease burden. This first-in-humans pilot study sets the stage for clinical trials employing adoptive transfer in the context of minimal residual disease.
转移性神经母细胞瘤是一种发生于儿童期的预后不良的恶性肿瘤,其L1细胞黏附分子(CD171)过度表达。我们之前描述了一种肿瘤L1细胞黏附分子特异性的、源自单链抗体的嵌合抗原受体,命名为CE7R,用于重新引导溶细胞性T淋巴细胞的抗原特异性效应功能。在此,我们报告在复发性/难治性神经母细胞瘤患儿中分离共表达CE7R和选择-自杀表达酶HyTK的自体CD8(+)溶细胞性T淋巴细胞克隆的可行性及输注安全性。溶细胞性T淋巴细胞产物源自外周血单个核细胞,这些细胞经过多克隆激活、质粒载体电穿孔、有限稀释潮霉素筛选以及扩增至足以进行过继转移的数量。总共对6例患者进行了12次输注(9次为10(8)个细胞/m(2),3次为10(9)个细胞/m(2))。未观察到对已知表达L1细胞黏附分子的组织(如中枢神经系统、肾上腺髓质和交感神经节)有明显毒性。通过载体特异性定量聚合酶链反应测量,溶细胞性T淋巴细胞克隆在循环中的持续时间在肿瘤负荷大的患者中较短(1 - 7天),但在疾病负担有限的患者中明显更长(42天)。这项首次人体试验性研究为在微小残留病背景下采用过继转移的临床试验奠定了基础。