首页> 美国卫生研究院文献>Infection and Immunity >Antibodies against Hemolysin and Cytotoxic Necrotizing Factor Type 1 (CNF1) Reduce Bladder Inflammation in a Mouse Model of Urinary Tract Infection with Toxigenic Uropathogenic Escherichia coli
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Antibodies against Hemolysin and Cytotoxic Necrotizing Factor Type 1 (CNF1) Reduce Bladder Inflammation in a Mouse Model of Urinary Tract Infection with Toxigenic Uropathogenic Escherichia coli

机译:抗溶血素和细胞毒性坏死因子1型(CNF1)的抗体可降低泌尿道感染毒原性致病性大肠杆菌的小鼠模型中的膀胱炎症。

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摘要

Uropathogenic Escherichia coli (UPEC) is the leading cause of cystitis. Cytotoxic necrotizing factor 1 (CNF1) and hemolysin (Hly) are toxins made by approximately 50% of UPEC isolates. CNF1 and Hly contribute to the robust inflammatory response in the bladders of mice challenged with UPEC strain CP9. We hypothesized that antibodies against CNF1 and/or Hly would reduce cystitis caused by CP9. To test this theory, we immunized female C3H/HeOuJ mice subcutaneously with a genetically derived Hly toxoid or genetically derived CNF1 toxoid plus sublethal doses of CNF1. We collected serum and observed increasing titers of specific and neutralizing antibodies against Hly or CNF1 over time. We challenged the mice intraurethrally with CP9 and euthanized them 24 h later. We observed 10-fold lower bacterial titers in the urine of Hly-immunized mice than in that of sham-immunized mice but no difference in kidney bacterial titers. Immunized mice also exhibited significantly less cystitis than sham-immunized mice. In CNF1-vaccinated mice, we detected neither a difference in urine or kidney bacterial titers nor a reduction in the severity of cystitis versus that of sham-immunized mice. We then passively administered an anti-CNF1 monoclonal antibody intraperitoneally to female C3H/HeOuJ mice prior to intraurethral challenge with CP9. Upon challenge, we noted no difference in colonization of the urine or kidney; however, cystitis was reduced significantly in mice treated with the anti-CNF1 antibody versus that in the bladders of mice given an isotype control antibody. Taken together, our data demonstrate that antibodies against CNF1 or Hly reduce the bladder pathology caused by UPEC.
机译:尿毒症性大肠杆菌(UPEC)是膀胱炎的主要原因。细胞毒性坏死因子1(CNF1)和溶血素(Hly)是大约50%的UPEC分离物产生的毒素。 CNF1和Hly有助于UPEC品系CP9攻击的小鼠膀胱中强烈的炎症反应。我们假设抗CNF1和/或Hly的抗体会减少CP9引起的膀胱炎。为了验证这一理论,我们用遗传衍生的Hly类毒素或遗传衍生的CNF1类毒素加上亚致死剂量的CNF1皮下免疫了雌性C3H / HeOuJ小鼠。我们收集了血清,观察到随着时间的推移,针对Hly或CNF1的特异性抗体和中和抗体的滴度增加。我们用CP9对小鼠进行尿道内攻击,并在24小时后对其实施安乐死。我们观察到,Hly免疫小鼠的尿液细菌滴度比假免疫小鼠低10倍,但肾脏细菌滴度无差异。免疫小鼠也比假免疫小鼠表现出明显更少的膀胱炎。在CNF1疫苗接种的小鼠中,与假免疫小鼠相比,我们既未检测到尿液或肾脏细菌滴度的差异,也未检测到膀胱炎的严重性降低。然后,我们在用CP9进行尿道内攻击之前,对雌性C3H / HeOuJ小鼠腹膜内被动给予抗CNF1单克隆抗体。挑战后,我们注意到尿液或肾脏的定植没有差异。然而,与使用同型对照抗体的小鼠膀胱相比,用抗CNF1抗体治疗的小鼠膀胱炎明显减少。综上所述,我们的数据表明针对CNF1或Hly的抗体可减轻UPEC引起的膀胱病理。

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