Bacteriology Laboratory, Butantan Institute, São Paulo, SP, Brazil.
Toxins (Basel). 2012 Sep;4(9):729-47. doi: 10.3390/toxins4090729. Epub 2012 Sep 18.
Monoclonal antibodies (MAbs) have been employed either for diagnosis or treatment of infections caused by different pathogens. Specifically for Shiga toxin-producing Escherichia coli (STEC), numerous immunoassays have been developed for STEC diagnosis, showing variability in sensitivity and specificity when evaluated by reference laboratories, and no therapy or vaccines are currently approved. Thus, the aim of this work was the characterization of the interaction between MAbs against Stx1 and Stx2 toxins and their neutralizing abilities to enable their use as tools for diagnosis and therapy. The selected clones designated 3E2 (anti-Stx1) and 2E11 (anti-Stx2) were classified as IgG1. 3E2 recognized the B subunit of Stx1 with an affinity constant of 2.5 × 10(-10) M, detected as little as 6.2 ng of Stx1 and was stable up to 50 ºC. In contrast, 2E11 recognized the A subunit of Stx2, was stable up to 70 ºC, had a high dissociation constant of 6.1 × 10(-10) M, and detected as little as 12.5 ng of Stx2. Neutralization tests showed that 160 ng of 3E2 MAb inhibited 80% of Stx1 activity and 500 µg 2E11 MAb were required for 60% inhibition of Stx2 activity. These MAb amounts reversed 25 to 80% of the cytotoxicity triggered by different STEC isolates. In conclusion, these MAbs show suitable characteristics for their use in STEC diagnosis and encourage future studies to investigate their protective efficacy.
单克隆抗体 (MAbs) 已被用于诊断或治疗由不同病原体引起的感染。特别是对于产志贺毒素大肠杆菌 (STEC),已经开发出许多免疫测定法用于 STEC 诊断,在经过参考实验室评估时,其敏感性和特异性存在差异,并且目前尚无治疗方法或疫苗获得批准。因此,本工作的目的是表征针对 Stx1 和 Stx2 毒素的 MAb 之间的相互作用及其中和能力,以使它们能够用作诊断和治疗工具。选定的克隆命名为 3E2(抗 Stx1)和 2E11(抗 Stx2),被归类为 IgG1。3E2 以 2.5×10(-10) M 的亲和力常数识别 Stx1 的 B 亚基,能够检测到低至 6.2 ng 的 Stx1,并且在 50°C 下稳定。相比之下,2E11 识别 Stx2 的 A 亚基,在 70°C 下稳定,具有高解离常数 6.1×10(-10) M,并且能够检测到低至 12.5 ng 的 Stx2。中和试验表明,160 ng 的 3E2 MAb 抑制了 80%的 Stx1 活性,而 500 µg 的 2E11 MAb 则需要 60%抑制 Stx2 活性。这些 MAb 量逆转了不同 STEC 分离株引起的细胞毒性的 25%至 80%。总之,这些 MAb 显示出适合用于 STEC 诊断的特征,并鼓励未来的研究调查其保护效力。