Centre for Molecular Therapeutics, Australian Institute of Tropical Health and Medicine, James Cook University, Cairns, QLD, Australia.
Wellcome Centre for Molecular Parasitology, Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, United Kingdom.
Int J Parasitol. 2021 Dec;51(13-14):1243-1253. doi: 10.1016/j.ijpara.2021.11.001. Epub 2021 Nov 10.
The major soil-transmitted helminths that infect humans are the roundworms, whipworms and hookworms. Soil-transmitted helminth infections rank among the most important neglected tropical diseases in terms of morbidity, and almost one billion people are still infected with at least one species. While anthelmintic drugs are available, they do not offer long term protection against reinfection, precipitating the need for vaccines that provide long-term immunologic defense. Vaccine discovery and development is in advanced clinical development for hookworm infection, with a bivalent human hookworm vaccine in clinical trials in Brazil and Africa, but is in its infancy for both roundworm (ascariasis) and whipworm (trichuriasis) infections. One of the greatest hurdles to developing soil-transmitted helminth vaccines is the potent immunoregulatory properties of these helminths, creating a barrier to the induction of meaningful long-term protective immunity. While challenging for vaccinologists, this phenomenon presents unique opportunities to develop an entirely new class of anti-inflammatory drugs that capitalise on these immunomodulatory strategies. Epidemiologic studies and clinical trials employing experimental soil-transmitted helminth challenge models, when coupled with findings from animal models, show that at least some soil-transmitted helminth-derived molecules can protect against the onset of autoimmune, allergic and metabolic disorders, and several natural products with the desired bioactivity have been isolated and tested in pre-clinical settings. The yin and yang of soil-transmitted helminth infections reflect both the urgency for effective vaccines and the potential for new immunoregulatory molecules from parasite products.
主要的土源性人体寄生虫包括蛔虫、鞭虫和钩虫。就发病率而言,土源性人体寄生虫感染是最重要的被忽视热带病之一,仍有近 10 亿人受到至少一种此类寄生虫的感染。虽然有驱虫药物,但它们不能提供针对再次感染的长期保护,因此需要开发能提供长期免疫防御的疫苗。钩虫感染的疫苗研发已进入临床开发的高级阶段,巴西和非洲正在进行两价人钩虫疫苗的临床试验,但蛔虫(蛔虫病)和鞭虫(鞭虫病)感染的疫苗研发仍处于起步阶段。开发土源性人体寄生虫疫苗的最大障碍之一是这些寄生虫具有强大的免疫调节特性,这阻碍了诱导有意义的长期保护性免疫。尽管对疫苗学家来说具有挑战性,但这种现象为开发全新类别的抗炎药物提供了独特的机会,这些药物利用了这些免疫调节策略。采用实验性土源性人体寄生虫感染挑战模型进行的流行病学研究和临床试验,结合动物模型的研究结果表明,至少某些土源性人体寄生虫来源的分子可以预防自身免疫、过敏和代谢紊乱的发生,并且已经从寄生虫产物中分离和测试了几种具有所需生物活性的天然产物。土源性人体寄生虫感染的“阴阳两面”既反映了有效疫苗的紧迫性,也反映了寄生虫产物中新型免疫调节分子的潜力。