Electrocardiogram Room, First Affiliated Hospital of Gannan Medical University, Ganzhou 341000, P.R. China.
Xingguo County Maternal and Child Health Hospital, Xingguo 342400, P.R. China.
Biomacromolecules. 2024 Jul 8;25(7):4557-4568. doi: 10.1021/acs.biomac.4c00556. Epub 2024 Jun 20.
Rheumatoid arthritis (RA) is a complicated chronic disorder of the immune system, featured with severe inflammatory joints, synovium hyperplasia, articular cartilage, and bone damage. In the RA microenvironment, RA-involved cells, overproduced nitric oxide (NO), and pro-inflammatory cytokines are highly interplayed and mutually reinforced, which form a vicious circle and play crucial roles in the formation and progression of RA. To comprehensively break the vicious circle and obtain the maximum benefits, we have developed neutrophil membrane-camouflaged NO scavenging nanoparticles based on an NO-responsive hyaluronic acid derivative for delivery of MTX. These multifunctional nanoparticles (NNO-NPs/MTX), by inheriting the membrane functions of the source cells, possess prolonged circulation and specific localization at the inflamed sites when administrated in the body. Remarkably, NNO-NPs/MTX can neutralize the pro-inflammatory cytokines via the outer membrane receptors, scavenge NO, and be responsively disassociated to release MTX for RA-involved cell regulation and HA for lubrication in the RA sites. In a collagen-induced arthritis mouse model, NNO-NPs/MTX exhibits a significant anti-inflammation effect and effectively alleviates the characteristic RA symptoms such as synovial hyperplasia and cartilage destruction, realizing the synergistic and boosted therapeutic outcome against intractable RA. Thus, NNO-NPs/MTX provides a promising and potent platform to integrately treat RA.
类风湿性关节炎(RA)是一种复杂的慢性免疫系统紊乱疾病,其特征为严重的炎症关节、滑膜增生、关节软骨和骨损伤。在 RA 微环境中,RA 相关细胞、过度产生的一氧化氮(NO)和促炎细胞因子高度相互作用和相互加强,形成恶性循环,在 RA 的形成和进展中发挥关键作用。为了全面打破恶性循环并获得最大效益,我们开发了基于 NO 响应透明质酸衍生物的中性粒细胞膜伪装的 NO 清除纳米粒子,用于输送 MTX。这些多功能纳米粒子(NNO-NPs/MTX)通过继承源细胞的膜功能,在体内给药时具有延长的循环时间和在炎症部位的特异性定位。值得注意的是,NNO-NPs/MTX 可以通过外膜受体中和促炎细胞因子,清除 NO,并响应性解离以释放 MTX 用于调节 RA 相关细胞,以及用于 RA 部位的润滑。在胶原诱导的关节炎小鼠模型中,NNO-NPs/MTX 表现出显著的抗炎作用,并有效缓解 RA 的特征性症状,如滑膜增生和软骨破坏,实现了针对难治性 RA 的协同和增强治疗效果。因此,NNO-NPs/MTX 为综合治疗 RA 提供了一个有前途和有效的平台。