Ragupathi Govind, Koide Fusataka, Sathyan Natarajan, Kagan Ella, Spassova Maria, Bornmann William, Gregor Polly, Reis Celso A, Clausen Henrik, Danishefsky Samuel J, Livingston Philip O
Laboratory of Tumor Vaccinology, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.
Cancer Immunol Immunother. 2003 Oct;52(10):608-16. doi: 10.1007/s00262-003-0399-2. Epub 2003 Jun 17.
Previously using a series of monovalent vaccines, we demonstrated that the optimal method for inducing an antibody response against cancer cell-surface antigens is covalent conjugation of the antigens to keyhole limpet hemocyanin (KLH) and the use of a saponin adjuvant. We have prepared a heptavalent-KLH conjugate vaccine containing the seven epithelial cancer antigens GM2, Globo H, Lewis(y), TF(c), Tn(c), STn(c), and glycosylated MUC1. In preparation for testing this vaccine in the clinic, we tested the impact on antibody induction of administering the individual conjugates plus adjuvant compared with a mixture of the seven conjugates plus adjuvant, and of several variables thought to augment immunogenicity. These include approaches for decreasing suppressor cell activity or increasing helper T-lymphocyte activity (low dose cyclophosphamide or anti-CTLA-4 MAb), different saponin adjuvants at various doses (QS-21 and GPI-0100), and different methods of formulation (lyophilization and use of polysorbate 80). We find that: (1). Immunization with the heptavalent-KLH conjugate plus GPI-0100 vaccine induces antibodies against the seven antigens of comparable titer to those induced by the individual-KLH conjugate vaccines, high titers of antibodies against Tn (median ELISA titer IgM/IgG 320/10240), STn (640/5120), TF (320/10240), MUC1 (80/20480), and globo H (640/40); while lower titers of antibodies against Lewis(y)()(160/0) and only occasional antibodies against GM2 are induced. (2). These antibodies reacted with the purified synthetic antigens by ELISA, and with naturally expressed antigens on the cancer cell surface by FACS. (3). None of the approaches for further altering the suppressor cell/helper T-cell balance nor changes to the standard formulation by lyophilization or use of polysorbate 80 had any impact on antibody titers. (4). An optimal dose of saponin adjuvant, QS-21 (50 microg) or GPI-0100 (1000 microg), is required for optimal antibody titers. This heptavalent vaccine is sufficiently optimized for testing in the clinic.
此前,我们使用一系列单价疫苗证明,诱导针对癌细胞表面抗原的抗体反应的最佳方法是将抗原与钥孔戚血蓝蛋白(KLH)共价偶联,并使用皂苷佐剂。我们制备了一种七价KLH偶联疫苗,其包含七种上皮癌抗原GM2、Globo H、Lewis(y)、TF(c)、Tn(c)、STn(c)和糖基化MUC1。为准备在临床中测试这种疫苗,我们测试了与七种偶联物加佐剂的混合物相比,单独给予偶联物加佐剂对抗体诱导的影响,以及几种被认为可增强免疫原性的变量的影响。这些变量包括降低抑制细胞活性或增加辅助性T淋巴细胞活性的方法(低剂量环磷酰胺或抗CTLA-4单克隆抗体)、不同剂量的不同皂苷佐剂(QS-21和GPI-0100)以及不同的制剂方法(冻干和使用聚山梨酯80)。我们发现:(1)。用七价KLH偶联物加GPI-0100疫苗免疫诱导的针对这七种抗原的抗体效价与单独的KLH偶联物疫苗诱导的抗体效价相当,针对Tn(酶联免疫吸附测定法(ELISA)IgM/IgG中位效价320/10240)、STn(640/5120)、TF(320/10240)、MUC1(80/20480)和Globo H(640/40)产生高滴度抗体;而针对Lewis(y)(160/0)的抗体滴度较低,仅偶尔诱导出针对GM2的抗体。(2)。这些抗体通过ELISA与纯化的合成抗原反应,并通过荧光激活细胞分选术(FACS)与癌细胞表面天然表达的抗原反应。(3)。进一步改变抑制细胞/辅助性T细胞平衡的方法,以及通过冻干或使用聚山梨酯80改变标准制剂的方法,均未对抗体滴度产生任何影响。(4)。为获得最佳抗体滴度,需要最佳剂量的皂苷佐剂QS-21(50微克)或GPI-0100(1000微克)。这种七价疫苗已充分优化,可用于临床测试。