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首页> 外文期刊>The journal of immunology >Antibody-Dependent Cell-Mediated Cytotoxicity- and Complement-Dependent Cytotoxicity-Independent Bactericidal Activity of an IgG against Pseudomonas aeruginosa O6ad
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Antibody-Dependent Cell-Mediated Cytotoxicity- and Complement-Dependent Cytotoxicity-Independent Bactericidal Activity of an IgG against Pseudomonas aeruginosa O6ad

机译:IgG对铜绿假单胞菌O6ad的抗体依赖性细胞介导的细胞毒性和补体依赖性细胞毒性非依赖性杀菌活性

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摘要

In addition to Ag recognition, some Abs are capable of killing target organisms in the absence of phagocytes and complement. In this study, we report that an anti- Pseudomonas aeruginosa O6ad LPS IgG1, tobacco-expressed human S20 IgG1 (te-hS20), as well as its recombinant Fab and single-chain variable fragment (scFv) fragments have cellular- and complement-independent bactericidal activity. te-hS20 and its Fab and scFv significantly reduced viability of P. aeruginosa O6ad in dose- and time-dependent manners in vitro and also showed lower levels of bactericidal activity against P. aeruginosa PAO1, but had no activity against P. aeruginosa O10, Escherichia coli TG1, and Streptococcus agalactiae . The H chain and its Fd fragment both had significant Ag-binding and bactericidal activities against P. aeruginosa O6ad. Bactericidal activity was completely inhibited with specific LPS Ag, suggesting that Ag binding is involved in the bactericidal mechanism. Live/dead cell staining and electron microscopic observations indicate that the bactericidal effect was due to disruption of the cell wall and suggest inhibition of cell division. In addition to te-hS20, the Fab and scFv were also protective in vivo, as leukopenic mice had prolonged and improved survival after administration of these Ab fragments followed by challenge with P. aeruginosa O6ad cells at 80–90% lethal dose, supporting a bactericidal mechanism independent of phagocytes and complement. Understanding of the bactericidal mechanism will allow assessment of the potential for therapeutic application of these Abs.
机译:除了对Ag的识别外,某些Abs还能在吞噬细胞和补体不存在的情况下杀死目标生物。在这项研究中,我们报告了抗铜绿假单胞菌O6ad LPS IgG1,烟草表达的人S20 IgG1(te-hS20)以及其重组Fab和单链可变片段(scFv)片段具有细胞和补体-独立的杀菌活性。 te-hS20及其Fab和scFv在体外以剂量和时间依赖性方式显着降低了铜绿假单胞菌O6ad的活力,并且对铜绿假单胞菌PAO1的杀菌活性较低,但对铜绿假单胞菌O10无活性,大肠杆菌TG1和无乳链球菌。 H链及其Fd片段均具有显着的Ag结合和针对铜绿假单胞菌O6ad的杀菌活性。特定的LPS Ag完全抑制了杀菌活性,这表明Ag的结合参与了杀菌机理。活/死细胞染色和电子显微镜观察表明,杀菌作用是由于细胞壁的破坏,提示细胞分裂受到抑制。除了te-hS20外,Fab和scFv还在体内具有保护作用,因为在施用这些Ab片段后,以80-90%致死剂量的铜绿假单胞菌O6ad细胞攻击后,白细胞减少症小鼠延长并改善了存活率,从而支持了杀菌机制独立于吞噬细胞和补体。了解杀菌机理将有助于评估这些抗体的治疗应用潜力。

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