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Large intestine-targeted nanoparticle-releasing oral vaccine to control genitorectal viral infection

机译:大肠靶向纳米粒子释放口服疫苗以控制genitorectal病毒感染

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摘要

Both rectal and vaginal mucosal surfaces serve as transmission routes for pathogenic microorganisms. Vaccination through large intestinal mucosa, previously proven protective for both mucosal sites in animal studies, can be achieved successfully by direct intra-colorectal (i.c.r.) administration, which is, however, clinically impractical. Oral delivery seems preferable, but risks vaccine destruction in the upper gastrointestinal tract. Therefore, we designed a large intestine-targeted oral delivery with pH-dependent microparticles containing vaccine nanoparticles, which induced colorectal immunity in mice comparably to colorectal vaccination and protected against rectal or vaginal viral challenge. Conversely, vaccine targeted to the small intestine induced only small intestinal immunity and provided no rectal or vaginal protection, demonstrating functional compartmentalization within the gut mucosal immune system. Therefore, using this oral vaccine delivery system to target the large intestine, but not the small intestine, may represent a feasible novel strategy for immune protection of rectal and vaginal mucosa.
机译:直肠和阴道粘膜表面均充当病原微生物的传播途径。通过大肠粘膜接种疫苗(先前已在动物研究中证明对两个粘膜部位均具有保护作用)可以通过直接大肠内(i.c.r.)施用而成功实现,但这在临床上是不切实际的。口服给药似乎是可取的,但可能会破坏上消化道的疫苗。因此,我们设计了一种含疫苗纳米颗粒的pH依赖性微粒,可通过大肠靶向口服给药,与小鼠的大肠疫苗相比,它可诱导小鼠的大肠免疫,并能抵抗直肠或阴道病毒攻击。相反,针对小肠的疫苗仅引起小肠免疫,没有提供直肠或阴道保护,这证明了肠道粘膜免疫系统的功能分区。因此,使用这种口服疫苗递送系统靶向大肠而非小肠可能是代表一种可行的新颖策略,用于直肠和阴道粘膜的免疫保护。

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