Unit for Immunopathology, Department of Clinical Chemistry and Clinical Pharmacology, University Hospital Bonn, University of Bonn, 53127, Bonn, Germany.
Mucosal Immunol. 2022 Jun;15(6):1234-1242. doi: 10.1038/s41385-022-00559-y. Epub 2022 Aug 31.
Helminths are multicellular ancient organisms residing as parasites at mucosal surfaces of their host. Through adaptation and co-evolution with their hosts, helminths have been able to develop tolerance mechanisms to limit inflammation and avoid expulsion. The study of helminth infections as an integral part of tissue immunology allowed us to understand fundamental aspects of mucosal and barrier immunology, which led to the discovery of a new group of tissue-resident immune cells, innate lymphoid cells (ILC), over a decade ago. Here, we review the intricate interplay between helminth infections and type 2 ILC (ILC2) biology, discuss the host metabolic adaptation to helminth infections and the metabolic pathways fueling ILC2 responses. We hypothesize that nutrient competition between host and helminths may have prevented chronic inflammation in the past and argue that a detailed understanding of the metabolic restraints imposed by helminth infections may offer new therapeutic avenues in the future.
蠕虫是多细胞的古老生物,以寄生虫的形式寄居在宿主的黏膜表面。通过与宿主的适应和共同进化,蠕虫已经能够发展出耐受机制,以限制炎症反应并避免被驱逐。将蠕虫感染作为组织免疫学的一个组成部分进行研究,使我们能够理解黏膜和屏障免疫学的基本方面,这导致了十多年前发现了一组新的组织驻留免疫细胞,即先天淋巴细胞 (ILC)。在这里,我们综述了蠕虫感染和 2 型先天淋巴细胞 (ILC2) 生物学之间的复杂相互作用,讨论了宿主对蠕虫感染的代谢适应以及为 ILC2 反应提供燃料的代谢途径。我们假设,宿主和蠕虫之间的营养竞争可能在过去阻止了慢性炎症,并认为详细了解蠕虫感染施加的代谢限制可能为未来提供新的治疗途径。