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Production of anti-neurotoxin antibody is enhanced by two subcomponents, HA1 and HA3b, of Clostridium botulinum type B 16S toxin–haemagglutinin

机译:通过两个子组件,Ha1和Ha3b,梭菌肉毒杆菌型B 16S毒素-Hemagglutinin的两种子组分,Ha1和Ha3b产生抗神经毒素抗体的产生

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Clostridium botulinum type B strain produces two forms of progenitor toxin, 16S and 12S. The 12S toxin is formed by association of a neurotoxin (NTX) and a non-toxic non-haemagglutinin (NTNH), and the 16S toxin is formed by conjugation of the 12S toxin with a haemagglutinin (HA). HA consists of four subcomponents designated HA1, HA2, HA3a and HA3b. When mice were immunized with formalin-detoxified NTX, 12S or 16S, a significantly greater amount of anti-NTX antibody (Ab) was produced in the mice injected with 16S than in NTX- or 12S-injected mice. Immunization with NTX mixed with HA1 and/or HA3b also increased the anti-NTX Ab production, whereas NTX mixed with HA2 did not, indicating that HA1 and HA3b have adjuvant activity. This was further confirmed by immunizing mice with human albumin (Alb) alone or Alb mixed with either HA1 or HA3b. When mouse-spleen cells were stimulated with NTX, 16S or different HA subcomponents, 16S, HA1, HA3b and the mixture of HA1 and HA3 significantly increased interleukin 6 (IL6) production compared with NTX alone. Transcription of IL6 mRNA was low after stimulation with NTX alone, but increased to 16S-stimulation levels when NTX was mixed with HA1 or HA3b. In flow cytometry using labelled Abs against CD3 and CD19, the percentage of CD19 cells was higher following stimulation with 16S or NTX mixed with HA1 or HA3b compared with stimulation with NTX. The percentage of CD3 cells remained unchanged. These results suggest strongly that HA1 and HA3b demonstrate adjuvant activity via increasing IL6 production.
机译:Bltridium botulinum型菌株产生两种形式的祖毒素,16s和12s。通过神经毒素(NTX)和无毒非血凝素(NTNH)的关联形成12S毒素,并且通过用Hemagglutinin(HA)将12S毒素缀合而形成16S毒素。 HA由四个子组件组成,指定HA1,HA2,HA3A和HA3B。当用福尔马林 - 解毒的NTX,12s或16s免疫小鼠时,在注射16s的小鼠中产生显着更大的抗NTX抗体(AB),而不是在NTX-或12S注入的小鼠中。用NTX与HA1和/或HA3B混合的免疫也增加了抗NTX AB的产生,而NTX与HA2混合并没有,表明HA1和HA3B具有佐剂活性。通过用单独的人白蛋白(ALB)免疫小鼠或与HA1或HA3B混合的ALB的免疫小鼠进一步证实。当用NTX,16s或不同的HA子组件刺激小鼠脾细胞,16s,Ha1,Ha 3b和Ha1和Ha3的混合物显着增加了与单独的NTX相比的白细胞介素6(IL6)的产生。当NTX与HA1或HA3B混合时,用NTX刺激,促射在NTX刺激后,IL6 mRNA的转录低至16S刺激水平。在流式细胞仪中使用标记的ABS反对CD3和CD19,在与HA1或HA3b的刺激与HA1或HA3B与NTX刺激相比,CD19细胞的百分比较高。 CD3细胞的百分比保持不变。这些结果表明,HA1和HA3B通过增加IL6生产来证明佐剂活性。

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