Tissue Engineering and Regenerative Medicine, University Hospital Würzburg, Würzburg, Germany.
Molecular Parasitology, Lindsley F. Kimball Research Institute, New York Blood Center, New York, New York, United States of America.
PLoS Negl Trop Dis. 2020 Nov 5;14(11):e0008503. doi: 10.1371/journal.pntd.0008503. eCollection 2020 Nov.
Onchocerciasis also known as river blindness is a neglected tropical disease and the world's second-leading infectious cause of blindness in humans; it is caused by Onchocerca volvulus. Current treatment with ivermectin targets microfilariae and transmission and does not kill the adult parasites, which reside within subcutaneous nodules. To support the development of macrofilaricidal drugs that target the adult worm to further support the elimination of onchocerciasis, an in-depth understanding of O. volvulus biology especially the factors that support the longevity of these worms in the human host (>10 years) is required. However, research is hampered by a lack of access to adult worms. O. volvulus is an obligatory human parasite and no small animal models that can propagate this parasite were successfully developed. The current optimized 2-dimensional (2-D) in vitro culturing method starting with O. volvulus infective larvae does not yet support the development of mature adult worms. To overcome these limitations, we have developed and applied 3-dimensional (3-D) culture systems with O. volvulus larvae that simulate the human in vivo niche using in vitro engineered skin and adipose tissue. Our proof of concept studies have shown that an optimized indirect co-culture of in vitro skin tissue supported a significant increase in growth of the fourth-stage larvae to the pre-adult stage with a median length of 816-831 μm as compared to 767 μm of 2-D cultured larvae. Notably, when larvae were co-cultured directly with adipose tissue models, a significant improvement for larval motility and thus fitness was observed; 95% compared to 26% in the 2-D system. These promising co-culture concepts are a first step to further optimize the culturing conditions and improve the long-term development of adult worms in vitro. Ultimately, it could provide the filarial research community with a valuable source of O. volvulus worms at various developmental stages, which may accelerate innovative unsolved biomedical inquiries into the parasite's biology.
盘尾丝虫病,又称河盲症,是一种被忽视的热带病,也是全球第二大致盲的人类传染病,由盘尾丝虫引起。目前,伊维菌素治疗针对微丝蚴和传播,而不能杀死成年寄生虫,这些寄生虫存在于皮下结节中。为了支持开发针对成虫的杀微丝蚴药物,以进一步支持消灭盘尾丝虫病,需要深入了解盘尾丝虫的生物学特性,特别是支持这些蠕虫在人类宿主中存活 10 年以上的因素。然而,由于无法获得成虫,研究受到了阻碍。盘尾丝虫是一种专性人体寄生虫,没有成功开发出能够繁殖这种寄生虫的小型动物模型。目前,从盘尾丝虫感染性幼虫开始的优化的二维(2-D)体外培养方法还不能支持成熟成虫的发育。为了克服这些限制,我们开发并应用了三维(3-D)培养系统,用体外工程皮肤和脂肪组织模拟人体体内小生境。我们的概念验证研究表明,优化的间接共培养体外皮肤组织显著增加了第四阶段幼虫向预成虫阶段的生长,中位数长度为 816-831μm,而 2-D 培养的幼虫为 767μm。值得注意的是,当幼虫直接与脂肪组织模型共培养时,观察到幼虫运动性显著提高,从而提高了适应性;95%,而 2-D 系统为 26%。这些有前途的共培养概念是进一步优化培养条件和提高成虫在体外长期发育的第一步。最终,它可以为丝虫病研究界提供各种发育阶段的盘尾丝虫虫源,这可能加速对寄生虫生物学的创新、未解决的生物医学研究。