Kalland T, Dohlsten M, Lind P, Sundstedt A, Abrahmsén L, Hedlund G, Björk P, Lando P A, Björklund M
Kabi Pharmacia Oncology, Lund, Sweden.
Med Oncol Tumor Pharmacother. 1993;10(1-2):37-47. doi: 10.1007/BF02987767.
We have developed a monoclonal antibody (mAb) based therapy intended for the treatment of solid tumors utilizing both main arms of the immune system by incorporating the colon carcinoma recognizing mAb C215 and the T cell activating bacterial staphylococcal enterotoxin A (SEA) in a single hybrid molecule. The recombinant tumor specific superantigen C215-SEA retained excellent antigen binding properties while the binding to MHC class II was markedly reduced and should allow targeting of a large fraction of T cells to tumors in vivo. C215-SEA mediated T cell killing of C215 expressing tumor cells irrespective of their expression of MHC class II antigens and induced levels of IFN-gamma and TNF in mononuclear cells sufficient to completely suppress the growth of colon carcinoma cells in vitro. In initial studies of anti-tumor effects, C215Fab-SEA was found to markedly inhibit the growth of colon carcinoma cells transplanted to Scid mice adoptively transferred with human mononuclear cells.
我们研发了一种基于单克隆抗体(mAb)的疗法,旨在通过将识别结肠癌的单克隆抗体C215和激活T细胞的细菌葡萄球菌肠毒素A(SEA)整合到一个单一的杂交分子中,利用免疫系统的两个主要分支来治疗实体瘤。重组肿瘤特异性超抗原C215-SEA保留了优异的抗原结合特性,而与II类主要组织相容性复合体(MHC)的结合则显著减少,这应能使体内大部分T细胞靶向肿瘤。C215-SEA介导表达C215的肿瘤细胞的T细胞杀伤,而不考虑其II类MHC抗原的表达,并在单核细胞中诱导产生足以在体外完全抑制结肠癌细胞生长的γ-干扰素(IFN-γ)和肿瘤坏死因子(TNF)水平。在抗肿瘤作用的初步研究中,发现C215Fab-SEA能显著抑制移植到用人单核细胞过继转移的重症联合免疫缺陷(Scid)小鼠体内的结肠癌细胞的生长。