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抗炭疽毒素单克隆抗体的组合在中和测定中表现出了新的特性。

Combinations of monoclonal antibodies to anthrax toxin manifest new properties in neutralization assays.

机构信息

Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, New York, USA.

出版信息

Infect Immun. 2013 Jun;81(6):1880-8. doi: 10.1128/IAI.01328-12. Epub 2013 Mar 18.

Abstract

Monoclonal antibodies (MAbs) are potential therapeutic agents against Bacillus anthracis toxins, since there is no current treatment to counteract the detrimental effects of toxemia. In hopes of isolating new protective MAbs to the toxin component lethal factor (LF), we used a strain of mice (C57BL/6) that had not been used in previous studies, generating MAbs to LF. Six LF-binding MAbs were obtained, representing 3 IgG isotypes and one IgM. One MAb (20C1) provided protection from lethal toxin (LeTx) in an in vitro mouse macrophage system but did not provide significant protection in vivo. However, the combination of two MAbs to LF (17F1 and 20C1) provided synergistic increases in protection both in vitro and in vivo. In addition, when these MAbs were mixed with MAbs to protective antigen (PA) previously generated in our laboratory, these MAb combinations produced synergistic toxin neutralization in vitro. But when 17F1 was combined with another MAb to LF, 19C9, the combination resulted in enhanced lethal toxicity. While no single MAb to LF provided significant toxin neutralization, LF-immunized mice were completely protected from infection with B. anthracis strain Sterne, which suggested that a polyclonal response is required for effective toxin neutralization. In total, these studies show that while a single MAb against LeTx may not be effective, combinations of multiple MAbs may provide the most effective form of passive immunotherapy, with the caveat that these may demonstrate emergent properties with regard to protective efficacy.

摘要

单克隆抗体(MAbs)是针对炭疽杆菌毒素的潜在治疗剂,因为目前没有治疗方法可以对抗毒血症的有害影响。为了分离针对毒素成分致死因子(LF)的新保护性 MAb,我们使用了一种以前的研究中未使用过的小鼠品系(C57BL/6),生成了 LF 的 MAb。获得了 6 种 LF 结合 MAb,代表 3 种 IgG 同种型和 1 种 IgM。一种 MAb(20C1)在体外小鼠巨噬细胞系统中提供了对致死毒素(LeTx)的保护,但在体内没有提供显著的保护。然而,两种 LF MAb(17F1 和 20C1)的组合在体外和体内都提供了协同的保护增加。此外,当这些 MAb 与我们实验室以前生成的保护性抗原(PA)的 MAb 混合时,这些 MAb 组合在体外产生协同的毒素中和作用。但是,当 17F1 与另一种 LF MAb,19C9 混合时,组合导致致死毒性增强。虽然没有单一的 LF MAb 提供显著的毒素中和作用,但 LF 免疫的小鼠完全免受炭疽杆菌菌株 Sterne 的感染,这表明需要多克隆反应才能有效中和毒素。总的来说,这些研究表明,虽然针对 LeTx 的单一 MAb 可能无效,但多种 MAb 的组合可能提供最有效的被动免疫治疗形式,但需要注意的是,这些可能会表现出对保护效果的新兴特性。

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