Ahnert-Hilger G, Bizzini B, Goretzki K, Müller H, Völckers C, Habermann E
Med Microbiol Immunol. 1983;172(2):123-35. doi: 10.1007/BF02124513.
Monoclonal antibodies against tetanus toxin and its toxoid were produced by immunizing mice with toxoid or toxin. They were measured by an enzyme-linked immunosorbent assay (ELISA), by a toxin neutralization test in mice (in vivo prevention test), and by their ability to prevent binding of 125I-toxin to brain membranes or gangliosides (in vitro prevention test). Six monoclonal antibodies obtained by immunization with toxoid (anti-toxoid 1-6) were investigated in more detail. They belonged to IgG class 1. Three of them (anti-toxoid 1, 2 and 3) recognized both toxoid and toxin as well as fragment B and the light chain of toxin, but not fragment C. Two other antibodies (anti-toxoid 4 and 5) were directed against toxoid only. Neither of them prevented toxin action in vitro or in vivo. Anti-toxoid 6 recognized toxin, toxoid and fragment C, but not light chain, and prevented toxin action in vitro and in vivo. Immunization against toxin was initiated with a toxin-antitoxin complex and boosted with toxin. We studied six antibodies in more detail, all of IgG type 2. Their KD against 125I-tetanus toxin varied from 10(-9) to 10(-10) M. Anti-toxin 2 recognized toxin, toxoid, light chain and fragment B, but not fragment C. The others reacted with toxin, toxoid and fragment C, but not with light chain or fragment B. All of them prevented toxin action in vitro and in vivo. As calculated from the maximal extinction achieved in the ELISA, tetanus toxin combined with a maximum of two different antibody molecules from our set. Gel filtration data indicate that tetanus toxin reacts with monoclonal antibodies one by one. Compared with polyclonal antiserum, monoclonal antibodies yield flatter slopes in both in vitro and in vivo prevention tests. Thus, they cannot substitute for the polyclonal antibodies in clinical situations, and cannot be calibrated in international units.
通过用类毒素或毒素免疫小鼠,制备了抗破伤风毒素及其类毒素的单克隆抗体。通过酶联免疫吸附测定法(ELISA)、小鼠体内毒素中和试验(体内预防试验)以及它们阻止¹²⁵I-毒素与脑膜或神经节苷脂结合的能力(体外预防试验)对这些抗体进行检测。对通过类毒素免疫获得的六种单克隆抗体(抗类毒素1-6)进行了更详细的研究。它们属于IgG1类。其中三种(抗类毒素1、2和3)能识别类毒素和毒素以及毒素的B片段和轻链,但不能识别C片段。另外两种抗体(抗类毒素4和5)仅针对类毒素。它们在体外或体内均不能阻止毒素作用。抗类毒素6能识别毒素、类毒素和C片段,但不能识别轻链,并能在体外和体内阻止毒素作用。用毒素-抗毒素复合物启动毒素免疫,并用毒素加强免疫。我们对六种均为IgG2型的抗体进行了更详细的研究。它们对¹²⁵I-破伤风毒素的解离常数(KD)在10⁻⁹至10⁻¹⁰M之间。抗毒素2能识别毒素、类毒素、轻链和B片段,但不能识别C片段。其他抗体与毒素、类毒素和C片段反应,但不与轻链或B片段反应。它们在体外和体内均能阻止毒素作用。根据ELISA中达到的最大吸光度计算,破伤风毒素最多可与我们所研究的两种不同抗体分子结合。凝胶过滤数据表明破伤风毒素与单克隆抗体逐个反应。与多克隆抗血清相比,单克隆抗体在体外和体内预防试验中的斜率更平缓。因此,在临床情况下它们不能替代多克隆抗体,也不能用国际单位进行校准。