Department of Immunology, University of Washington, Seattle, WA, 98117, USA.
Eur J Immunol. 2021 Oct;51(10):2399-2416. doi: 10.1002/eji.202048909. Epub 2021 Sep 7.
Type 2 immunity is critical for the protective and repair responses that mediate resistance to parasitic helminth infection. This immune response also drives aberrant inflammation during atopic diseases. Prostaglandins are a class of critical lipid mediators that are released during type 2 inflammation and are integral in controlling the initiation, activation, maintenance, effector functions, and resolution of Type 2 inflammation. In this review, we explore the roles of the different prostaglandin family members and the receptors they bind to during allergen- and helminth-induced Type 2 inflammation and the mechanism through which prostaglandins promote or suppress Type 2 inflammation. Furthermore, we discuss the potential role of prostaglandins produced by helminth parasites in the regulation of host-pathogen interactions, and how prostaglandins may regulate the inverse relationship between helminth infection and allergy. Finally, we discuss opportunities to capitalize on our understanding of prostaglandin pathways to develop new therapeutic options for humans experiencing Type 2 inflammatory disorders that have a significant prostaglandin-driven component including allergic rhinitis and asthma.
2 型免疫对于介导寄生虫蠕虫感染的抵抗的保护和修复反应至关重要。这种免疫反应也会导致特应性疾病中的异常炎症。前列腺素是一类关键的脂质介质,在 2 型炎症期间释放,并在控制 2 型炎症的起始、激活、维持、效应功能和消退中发挥重要作用。在这篇综述中,我们探讨了不同的前列腺素家族成员及其结合的受体在过敏原和蠕虫诱导的 2 型炎症中的作用,以及前列腺素促进或抑制 2 型炎症的机制。此外,我们讨论了寄生虫蠕虫产生的前列腺素在宿主-病原体相互作用中的调节作用,以及前列腺素如何调节蠕虫感染和过敏之间的反比关系。最后,我们讨论了利用我们对前列腺素途径的理解来开发针对人类 2 型炎症性疾病的新治疗选择的机会,这些疾病具有显著的前列腺素驱动成分,包括过敏性鼻炎和哮喘。