Bacelo Elisa, Alves da Silva Marta, Cunha Cristina, Faria Susana, Carvalho Agostinho, Reis Rui L, Martins Albino, Neves Nuno M
3B's Research Group, I3Bs-Research Institute of Biomaterials, Biodegradables and Biomimetics, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark-Parque de Ciência e Tecnologia, Zona Industrial da Gandra, University of Minho, Barco, 4805-017 Guimarães, Portugal.
ICVS/3B's-PT Government Associate Laboratory, Barco, 4805-017 Guimarães, Portugal.
Nanomaterials (Basel). 2019 Apr 8;9(4):567. doi: 10.3390/nano9040567.
Rheumatoid arthritis (RA) is an autoimmune disease that affects the synovial cavity of joints, and its pathogenesis is associated with an increased expression of pro-inflammatory cytokines, namely tumour necrosis factor-alpha (TNF-α). It has been clinically shown to have an adequate response to systemic administration of TNF-α inhibitors, although with many shortcomings. To overcome such limitations, the immobilization of a TNF-α antibody on a nanofibrous substrate to promote a localized action is herein proposed. By using this approach, the antibody has its maximum therapeutic efficacy and a prolonged therapeutic benefit, avoiding the systemic side-effects associated with conventional biological agents' therapies. To technically achieve such a purpose, the surface of electrospun nanofibers is initially activated and functionalized, allowing TNF-α antibody immobilization at a maximum concentration of 6 µg/mL. Experimental results evidence that the biofunctionalized nanofibrous substrate is effective in achieving a sustained capture of soluble TNF-α over time. Moreover, cell biology assays demonstrate that this system has no deleterious effect over human articular chondrocytes metabolism and activity. Therefore, the developed TNF-capturing system may represent a potential therapeutic approach for the local management of severely affected joints.
类风湿性关节炎(RA)是一种影响关节滑膜腔的自身免疫性疾病,其发病机制与促炎细胞因子表达增加有关,即肿瘤坏死因子-α(TNF-α)。临床上已表明,全身给予TNF-α抑制剂有一定疗效,尽管存在许多缺点。为克服这些局限性,本文提出将TNF-α抗体固定在纳米纤维基质上以促进局部作用。通过这种方法,抗体具有最大治疗效果和延长的治疗益处,避免了与传统生物制剂疗法相关的全身副作用。为从技术上实现这一目的,首先对静电纺丝纳米纤维的表面进行活化和功能化,使TNF-α抗体以最高6μg/mL的浓度固定。实验结果表明,生物功能化的纳米纤维基质能有效实现对可溶性TNF-α的持续捕获。此外,细胞生物学检测表明该系统对人关节软骨细胞的代谢和活性没有有害影响。因此,所开发的TNF捕获系统可能代表一种对严重受累关节进行局部治疗的潜在方法。