Kageyama Shinichi, Kitano Shigehisa, Hirayama Michiko, Nagata Yasuhiro, Imai Hiroshi, Shiraishi Taizo, Akiyoshi Kazunari, Scott Andrew M, Murphy Roger, Hoffman Eric W, Old Lloyd J, Katayama Naoyuki, Shiku Hiroshi
Department of Immuno-Gene Therapy, Mie University Graduate School of Medicine, 2-174 Edobashi, Tsu, Mie 514-8507, Japan.
Cancer Sci. 2008 Mar;99(3):601-7. doi: 10.1111/j.1349-7006.2007.00705.x. Epub 2007 Dec 15.
The CHP-HER2 vaccine, comprising truncated 146HER2 protein complexed with nanogels of cholesteryl pullulan (CHP), is a novel protein antigen vaccine that elicits 146HER2-specific CD8(+) and CD4(+) T-cell immune responses in patients with HER2-expressing tumors. We analyzed the humoral responses in patients vaccinated with CHP-HER2 and those with CHP-HER2 plus granulocyte-macrophage colony-stimulating factor (GM-CSF). The vaccine was injected subcutaneously at a dose of 300 microg protein. Nine patients received the vaccine alone over the first four injections, followed by CHP-HER2 with GM-CSF or OK-432, whereas six received CHP-HER2 plus GM-CSF from the first cycle. 146HER2-specific IgG antibodies were induced in 14 patients, who were negative at baseline. The antibodies became detectable after the second or third vaccination and reached plateau levels after the third or fourth cycle in patients vaccinated with CHP-HER2 plus GM-CSF. In contrast, the antibodies appeared only after the third to sixth vaccination and the plateau appeared after the fourth to eighth cycle in patients vaccinated with the CHP-HER2 vaccine alone over the first four cycles. The antibodies induced by the vaccine were not reactive with HER2 antigen expressed on the cell surface in any of the patients. Epitope analysis using overlapping peptides revealed a single region in the 146HER2 protein, amino acids 127-146, in eight patients who were initially vaccinated with CHP-HER2 alone. Similarly, the same HER2 region was recognized dominantly in patients vaccinated with GM-CSF. Our results indicate that CHP-HER2 induced HER2-specific humoral responses in patients with HER2-expressing tumors and that GM-CSF seems to accelerate the responses.
CHP-HER2疫苗由截短的146HER2蛋白与胆固醇普鲁兰聚糖(CHP)纳米凝胶复合而成,是一种新型蛋白抗原疫苗,可在HER2表达肿瘤患者中引发146HER2特异性CD8(+)和CD4(+) T细胞免疫反应。我们分析了接种CHP-HER2疫苗以及接种CHP-HER2加粒细胞-巨噬细胞集落刺激因子(GM-CSF)的患者的体液反应。疫苗以300微克蛋白的剂量皮下注射。9名患者在前四次注射时单独接种疫苗,随后接种CHP-HER2加GM-CSF或OK-432,而6名患者从第一个周期开始就接种CHP-HER2加GM-CSF。14名基线时为阴性的患者诱导产生了146HER2特异性IgG抗体。在用CHP-HER2加GM-CSF接种的患者中,抗体在第二次或第三次接种后可检测到,并在第三次或第四次周期后达到平台期水平。相比之下,在最初四个周期单独接种CHP-HER2疫苗的患者中,抗体仅在第三次至第六次接种后出现,平台期在第四次至第八次周期后出现。疫苗诱导产生的抗体在任何患者中均不与细胞表面表达的HER2抗原发生反应。使用重叠肽进行的表位分析显示,在最初单独接种CHP-HER2的8名患者中,146HER2蛋白的127-146位氨基酸区域为单一表位。同样,在接种GM-CSF的患者中,相同的HER2区域也被主要识别。我们的结果表明,CHP-HER2在HER2表达肿瘤患者中诱导了HER2特异性体液反应,并且GM-CSF似乎加速了这些反应。