Chen A-Yuan, Zhao Ying-Jie, Wang Yue-Ye, Wei Wei, Hu Wei, Chang Yan
Institute of Clinical Pharmacology, Anhui Medical University, Key Laboratory of Anti-Inflammatory and Immune Medicine, Ministry of Education, Anhui Collaborative Innovation Center of Anti-Inflammatory and Immune Medicine, Hefei 230032, China.
The Second Affiliated Hospital of Anhui Medical University, Hefei 230032, China.
Exp Gerontol. 2025 Oct 1;209:112837. doi: 10.1016/j.exger.2025.112837. Epub 2025 Jul 16.
The kynurenine pathway (KP), a major metabolic pathway for L-tryptophan (Trp) in mammals, plays a multifaceted role in various physiological processes, including neural activity, immune system regulation, and the maintenance of intestinal homeostasis. The functional connection between the KP and immune system is supported by robust evidence, including disease-associated alterations in KP metabolite concentrations and enzyme activities that correlate with immune function changes. Imbalances in the KP can be detrimental, as excessive production of pro- or anti-inflammatory metabolites may promote autoimmunity or impair pathogen defense. To date, KP enzymes and metabolites have been extensively studied as both promoters and therapeutic targets in a wide array of autoimmune diseases (AID). Pharmacological modulation of the KP represents a promising therapeutic strategy, as it can regulate immune responses and attenuate disease progression in AID. However, the precise cellular and molecular mechanisms by which the KP contributes to AID pathogenesis remain incompletely understood. This review explores the complex mechanisms through which KP enzymes and metabolites regulate inflammatory immune responses in AID, and highlights potential therapeutic targets for drug development.
犬尿氨酸途径(KP)是哺乳动物中L-色氨酸(Trp)的主要代谢途径,在包括神经活动、免疫系统调节和肠道稳态维持在内的各种生理过程中发挥多方面作用。KP与免疫系统之间的功能联系有充分证据支持,包括与免疫功能变化相关的KP代谢物浓度和酶活性的疾病相关改变。KP失衡可能有害,因为促炎或抗炎代谢物的过度产生可能促进自身免疫或损害病原体防御。迄今为止,KP酶和代谢物作为多种自身免疫性疾病(AID)的促进剂和治疗靶点已得到广泛研究。对KP的药理调节是一种有前景的治疗策略,因为它可以调节免疫反应并减轻AID中的疾病进展。然而,KP促成AID发病机制的确切细胞和分子机制仍未完全了解。本综述探讨了KP酶和代谢物调节AID中炎症免疫反应的复杂机制,并强调了药物开发的潜在治疗靶点。