Livingston P O, Ragupathi G
Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York City, NY 10021, USA.
Cancer Immunol Immunother. 1997 Oct;45(1):10-9. doi: 10.1007/s002620050395.
The primary function of antibodies is the elimination of circulating viral or bacterial pathogens from the blood-stream, lymphatics and interstitial spaces, and so, once induced, antibodies should be ideally suited for eliminating tumor cells and micrometastases from these spaces as well. Natural or tumor-induced and vaccine-induced antibodies against human cancer-associated antigens have been correlated with an improved clinical outcome. In the mouse, passive administration of monoclonal antibodies against cell-surface antigens 1–4 days after tumor challenge, and active induction of antibodies with vaccines, has resulted in prolonged survival or complete protection from tumor growth. This is a setting similar to the adjuvant setting in humans. Carbohydrates are the most abundant antigens at the cell surface of cancer cells, where they play important roles in cell-cell interactions, proliferation and the metastatic process. They have been shown to be excellent targets for immune attack by antibodies against human cancers, especially in the adjuvant setting. Vaccines containing these carbohydrate antigens covalently attached to immunogenic carrier proteins, such as KLH, plus potent immunological adjuvants, such as QS-21, effectively induce antibodies against these antigens in patients, which can result in complement-mediated lysis of antigen-positive tumor cells. Phase III trials with KLH conjugate vaccines have been initiated in the adjuvant setting against two carbohydrate antigens, the ganglioside GM2 and the blood-group-related antigen sTn. As the immunogenicity of additional vaccines is confirmed in small pilot trials, trials with polyvalent vaccines against two to five different antigens tailored for particular cancer types are planned.
抗体的主要功能是清除血液、淋巴管和组织间隙中循环的病毒或细菌病原体,因此,一旦被诱导产生,抗体理论上也应同样适用于清除这些部位的肿瘤细胞和微转移灶。针对人类癌症相关抗原的天然抗体、肿瘤诱导产生的抗体以及疫苗诱导产生的抗体都与临床预后改善相关。在小鼠中,肿瘤攻击后1 - 4天被动给予针对细胞表面抗原的单克隆抗体,以及用疫苗主动诱导抗体产生,已导致生存期延长或完全免受肿瘤生长。这与人类的辅助治疗情况相似。碳水化合物是癌细胞表面最丰富的抗原,它们在细胞间相互作用、增殖和转移过程中发挥重要作用。它们已被证明是针对人类癌症进行免疫攻击的极佳靶点,尤其是在辅助治疗中。含有这些共价连接到免疫原性载体蛋白(如钥孔血蓝蛋白)上的碳水化合物抗原的疫苗,加上强效免疫佐剂(如QS - 21),能有效地在患者体内诱导针对这些抗原的抗体,这可导致补体介导的抗原阳性肿瘤细胞裂解。针对两种碳水化合物抗原(神经节苷脂GM2和血型相关抗原sTn)的钥孔血蓝蛋白共轭疫苗已在辅助治疗中启动III期试验。随着更多疫苗在小型试点试验中免疫原性得到证实,计划开展针对特定癌症类型定制的二价至五价疫苗试验。