Seferian P G, Rodkey L S
Department of Pathology and Laboratory Medicine, University of Texas Medical School, Houston 77225-0708.
Appl Biochem Biotechnol. 1994 May-Jun;47(2-3):213-26; discussion 226-7. doi: 10.1007/BF02787936.
In this study, immunization with a vaccine consisting of multiple F(ab')2 fragments of affinity-purified antitetanus toxoid antibodies covalently bound to a carrier protein successfully induced antitetanus toxoid antibodies. Further studies showed that this vaccine preparation contained no biologically detectable tetanus antigen. The induced antitetanus antibody (Ab1') titer was higher than the titer of antibodies binding control antigens. The immunizing F(ab')2 preparation did not elicit a secondary antitetanus response from mice primed with tetanus toxoid and, hence, appeared free of tetanus epitopes. The specificity of Ab1' was established by absorption and inhibition with antigen. Immunization with antitetanus F(ab')2 (Ab1') fragments appears to have elicited naturally occurring autologous antitetanus toxoid antibody (Ab1') through an idiotypic pathway. As predicted by network theory, anti-idiotype (Ab2) and antitetanus (Ab1') cycled reciprocally. Clonotypic characterization of Ab1' using isoelectric focusing and affinity immunoblotting showed increases in Ab1' titer to be the result of increased synthesis by limited subsets of antitetanus toxoid B-cell clones and not increased synthesis by multiple clones, as is characteristic of antigen-driven Ab1 responses. Many Ab1 and Ab1' clonotypes had identical pIs, suggesting that they either share V region genes or are the product of the same B-cell clones. These findings indicate that immunization with polyclonal multivalent Ab1 preparations can trigger active synthesis of antibodies with the same specificity. The results provide further evidence for naturally occurring idiotypic cascades that could be exploited for studies of catalytic antibodies.
在本研究中,用一种疫苗进行免疫接种,该疫苗由亲和纯化的抗破伤风类毒素抗体的多个F(ab')2片段共价结合到一种载体蛋白组成,成功诱导出抗破伤风类毒素抗体。进一步研究表明,这种疫苗制剂中没有生物学上可检测到的破伤风抗原。诱导产生的抗破伤风抗体(Ab1')滴度高于结合对照抗原的抗体滴度。免疫用的F(ab')2制剂未引发用破伤风类毒素致敏的小鼠产生二次抗破伤风反应,因此似乎不含破伤风表位。通过用抗原进行吸收和抑制来确定Ab1'的特异性。用抗破伤风F(ab')2(Ab1')片段进行免疫接种似乎通过独特型途径引发了天然存在的自身抗破伤风类毒素抗体(Ab1')。如网络理论所预测,抗独特型(Ab2)和抗破伤风(Ab1')相互循环。使用等电聚焦和亲和免疫印迹对Ab1'进行克隆型表征表明,Ab1'滴度的增加是由抗破伤风类毒素B细胞克隆的有限亚群合成增加所致,而不是像抗原驱动的Ab1反应那样由多个克隆合成增加所致。许多Ab1和Ab1'克隆型具有相同的等电点,这表明它们要么共享V区基因,要么是同一B细胞克隆的产物。这些发现表明,用多克隆多价Ab1制剂进行免疫接种可触发具有相同特异性的抗体的活性合成。这些结果为天然存在的独特型级联反应提供了进一步的证据,可用于催化抗体的研究。