Glenn Gregory M, Francis David H, Danielsen E Michael
Intercell USA, Inc, Gaithersburg, Maryland 20878, USA.
Infect Immun. 2009 Dec;77(12):5206-15. doi: 10.1128/IAI.00712-09. Epub 2009 Sep 8.
Recent studies have confirmed older observations that the enterotoxins enhance enteric bacterial colonization and pathogenicity. How and why this happens remains unknown at this time. It appears that toxins such as the heat-labile enterotoxin (LT) from Escherichia coli can help overcome the innate mucosal barrier as a key step in enteric pathogen survival. We review key observations relevant to the roles of LT and cholera toxin in protective immunity and the effects of these toxins on innate mucosal defenses. We suggest either that toxin-mediated fluid secretion mechanically disrupts the mucus layer or that toxins interfere with innate mucosal defenses by other means. Such a breach gives pathogens access to the enterocyte, leading to binding and pathogenicity by enterotoxigenic E. coli (ETEC) and other organisms. Given the common exposure to LT(+) ETEC by humans visiting or residing in regions of endemicity, barrier disruption should frequently render the gut vulnerable to ETEC and other enteric infections. Conversely, toxin immunity would be expected to block this process by protecting the innate mucosal barrier. Years ago, Peltola et al. (Lancet 338:1285-1289, 1991) observed unexpectedly broad protective effects against LT(+) ETEC and mixed infections when using a toxin-based enteric vaccine. If toxins truly exert barrier-disruptive effects as a key step in pathogenesis, then a return to classic toxin-based vaccine strategies for enteric disease is warranted and can be expected to have unexpectedly broad protective effects.
最近的研究证实了早期的观察结果,即肠毒素可增强肠道细菌的定植和致病性。目前尚不清楚其发生方式及原因。似乎诸如大肠杆菌不耐热肠毒素(LT)之类的毒素能够帮助克服先天性黏膜屏障,这是肠道病原体生存的关键步骤。我们回顾了与LT和霍乱毒素在保护性免疫中的作用以及这些毒素对先天性黏膜防御的影响相关的关键观察结果。我们认为,毒素介导的液体分泌会机械性破坏黏液层,或者毒素通过其他方式干扰先天性黏膜防御。这种破坏使病原体能够接触肠上皮细胞,导致产肠毒素大肠杆菌(ETEC)及其他微生物的黏附和致病。鉴于前往或居住在疾病流行地区的人经常接触LT(+) ETEC,屏障破坏应经常使肠道易受ETEC和其他肠道感染的影响。相反,毒素免疫有望通过保护先天性黏膜屏障来阻断这一过程。多年前,佩尔托拉等人(《柳叶刀》338:1285 - 1289, 1991)观察到,使用基于毒素的肠道疫苗时,对LT(+) ETEC和混合感染具有出人意料的广泛保护作用。如果毒素真的在发病机制中作为关键步骤发挥屏障破坏作用,那么回归经典的基于毒素的肠道疾病疫苗策略是有必要的,并且有望产生出人意料的广泛保护作用。