Thumsi Abhirami, Martínez Diego, Swaminathan Srivatsan J, Esrafili Arezoo, Suresh Abhirami P, Jaggarapu Madhan Mohan Chandrasekhar, Lintecum Kelly, Halim Michelle, Mantri Shivani V, Sleiman Yasmine, Appel Nicole, Gu Haiwei, Curtis Marion, Zuniga Cristal, Acharya Abhinav P
Department of Pathology, Case Western REserve University School of Medicine, Cleveland, OH, 44106, USA.
Department of Biology, San Diego State University, San Diego, CA, 92182, USA.
Adv Healthc Mater. 2025 Feb;14(5):e2303995. doi: 10.1002/adhm.202303995. Epub 2024 Mar 19.
Rheumatoid arthritis (RA) causes immunological and metabolic imbalances in tissue, exacerbating inflammation in affected joints. Changes in immunological and metabolic tissue homeostasis at different stages of RA are not well understood. Herein, the changes in the immunological and metabolic profiles in different stages in collagen induced arthritis (CIA), namely, early, intermediate, and late stage is examined. Moreover, the efficacy of the inverse-vaccine, paKG(PFK15+bc2) microparticle, to restore tissue homeostasis at different stages is also investigated. Immunological analyses of inverse-vaccine-treated group revealed a significant decrease in the activation of pro-inflammatory immune cells and remarkable increase in regulatory T-cell populations in the intermediate and late stages compared to no treatment. Also, glycolysis in the spleen is normalized in the late stages of CIA in inverse-vaccine-treated mice, which is similar to no-disease tissues. Metabolomics analyses revealed that metabolites UDP-glucuronic acid and L-Glutathione oxidized are significantly altered between treatment groups, and thus might provide new druggable targets for RA treatment. Flux metabolic modeling identified amino acid and carnitine pathways as the central pathways affected in arthritic tissue with CIA progression. Overall, this study shows that the inverse-vaccines initiate early re-establishment of homeostasis, which persists through the disease span.
类风湿性关节炎(RA)会导致组织中的免疫和代谢失衡,加剧受累关节的炎症。目前对RA不同阶段免疫和代谢组织稳态的变化尚不完全清楚。在此,研究了胶原诱导性关节炎(CIA)不同阶段,即早期、中期和晚期的免疫和代谢谱变化。此外,还研究了反向疫苗paKG(PFK15 + bc2)微粒在不同阶段恢复组织稳态的功效。反向疫苗治疗组的免疫分析显示,与未治疗组相比,在中期和晚期促炎免疫细胞的活化显著降低,调节性T细胞群体显著增加。而且,在反向疫苗治疗的小鼠中,CIA晚期脾脏中的糖酵解恢复正常,这与无疾病组织相似。代谢组学分析表明,治疗组之间代谢物UDP-葡萄糖醛酸和氧化型L-谷胱甘肽有显著变化,因此可能为RA治疗提供新的可成药靶点。通量代谢模型确定氨基酸和肉碱途径是随着CIA进展在关节炎组织中受影响的核心途径。总体而言,这项研究表明反向疫苗可启动稳态的早期重建,并在疾病过程中持续存在。