Chanh T C, Hewetson J F
Department of Virology and Immunology, Southwest Foundation for Biomedical Research, San Antonio, Texas 78228-0147.
Immunology. 1993 Aug;79(4):681-4.
Protein G-purified goat anti-ricin IgG, previously demonstrated to protect against ricin toxicity in vitro and in vivo, was used to raise BALB/c mouse and New Zealand White rabbit polyclonal anti-idiotypic antibodies. The generated anti-idiotypic sera were repeatedly absorbed over agarose conjugated to normal goat immunoglobulins, and purified by protein A-agarose affinity chromatography. Immunization of BALB/c mice with BALB/c anti-idiotypes did not result in a significant anti-ricin antibody response. However, injection of BALB/c mice with BALB/c anti-idiotypes conjugated to keyhole limpet haemocyanin (KLH) or with unconjugated rabbit anti-idiotypes resulted in specific and anti-ricin immune responses. The anti-idiotype-induced anti-ricin antibody responses protected against the in vitro cytotoxicity of ricin, a potent plant-derived protein synthesis inhibitor, as assessed by the murine EL-4 leukaemia cell assays. Thus, anti-idiotype-based vaccines may represent an alternative, safe and effective means of inducing protective immunity against toxins such as ricin, whose extreme in vivo toxicity render them unsafe as immunogens.
蛋白G纯化的山羊抗蓖麻毒素IgG先前已证明在体外和体内均能抵御蓖麻毒素毒性,用其制备BALB/c小鼠和新西兰白兔的多克隆抗独特型抗体。所产生的抗独特型血清在与正常山羊免疫球蛋白偶联的琼脂糖上反复吸收,并通过蛋白A-琼脂糖亲和层析进行纯化。用BALB/c抗独特型免疫BALB/c小鼠未产生显著的抗蓖麻毒素抗体反应。然而,给BALB/c小鼠注射与钥孔戚血蓝蛋白(KLH)偶联的BALB/c抗独特型或未偶联的兔抗独特型会产生特异性的抗蓖麻毒素免疫反应。通过小鼠EL-4白血病细胞试验评估,抗独特型诱导的抗蓖麻毒素抗体反应能抵御蓖麻毒素(一种强效的植物源性蛋白质合成抑制剂)的体外细胞毒性。因此,基于抗独特型的疫苗可能是诱导针对蓖麻毒素等毒素产生保护性免疫的一种安全有效的替代方法,蓖麻毒素在体内的极端毒性使其作为免疫原不安全。