首页> 外文期刊>FEMS Microbiology Letters >Enterotoxigenic Escherichia coli heat-stable toxin and heat-labile toxin toxoid fusion 3xSTa(N12S)-dmLT induces neutralizing anti-STa antibodies in subcutaneously immunized mice
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Enterotoxigenic Escherichia coli heat-stable toxin and heat-labile toxin toxoid fusion 3xSTa(N12S)-dmLT induces neutralizing anti-STa antibodies in subcutaneously immunized mice

机译:Enterotoxigenic大肠杆菌热稳定毒素和热稳定毒素类毒素融合3xsta(n12s)-dmlt在皮下免疫小鼠中诱导中和抗sta抗体

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摘要

Enterotoxigenic Escherichia coli (ETEC) bacteria producing heat-stable toxin (STa) and/or heat-labile toxin (LT) are among top causes of children's diarrhea and travelers' diarrhea. Currently no vaccines are available for ETEC associated diarrhea. A major challenge in developing ETEC vaccines is the inability to stimulate protective antibodies against the key STa toxin that is potently toxic and also poorly immunogenic. A recent study suggested toxoid fusion 3xSTa(N12S)-dmLT, which consists of a monomer LT toxoid (LTR192G/L211A) and three copies of STa toxoid STaN12S, may represent an optimal immunogen inducing neutralizing antibodies against STa toxin [IAI 2014, 82(5): 1823-32]. In this study, we immunized mice with this fusion protein following a different parenteral route and using different adjuvants to further characterize immunogenicity of this toxoid fusion. Data from this study showed that 3xSTa(N12S)-dmLT toxoid fusion induced neutralizing anti-STa antibodies in the mice following subcutaneous immunization, as effectively as in the mice under intraperitoneal route. Data also indicated that double mutant LT (dmLT) can be an effective adjuvant for this toxoid fusion in mice subcutaneous immunization. Results from this study affirmed that toxoid fusion 3xSTa(N12S)-dmLT induces neutralizing antibodies against STa toxin, suggesting this toxoid fusion is potentially a promising immunogen for ETEC vaccine development.
机译:产生热稳定毒素(STA)和/或热稳定毒素(LT)的肠毒素大肠杆菌(ETEC)细菌是儿童腹泻和旅行者腹泻的最大原因。目前没有可用于ETEC相关腹泻的疫苗。在开发ETEC疫苗方面的一项重大挑战是无法刺激对毒性的关键STA毒素的保护性抗体,这些毒素具有棘毒的毒性,也是较差的免疫原性。最近的研究表明毒素融合3XSTA(N12S)-DMLT,其由单体LT毒素(LTR192G / L211A)和三个STA类毒素术副本组成,可以代表一种致针对STA毒素的中和抗体的最佳免疫原性[IAI 2014,82( 5):1823-32]。在该研究中,我们用这种融合蛋白免疫小鼠在不同的肠胃外途径,并使用不同的佐剂进一步表征该毒素融合的免疫原性。本研究的数据显示,3xSTA(N12S)-DMLT毒素融合在皮下免疫后,如腹膜内途径下的小鼠那样有效地诱导小鼠的中和抗-STA抗体。数据还表明,双突变体LT(DMLT)可以是对小鼠皮下免疫的这种毒素融合的有效佐剂。本研究的结果肯定了毒素融合3XSTA(N12S)-DMLT诱导对STA毒素的中和抗体,表明这种无毒融合可能是ETEC疫苗发育的有希望的免疫原。

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