Smakaj Amarildo, Gasbarra Elena, Cardelli Tommaso, Salvati Chiara, Bonanni Roberto, Cariati Ida, Iundusi Riccardo, Tarantino Umberto
Department of Biomedicine and Prevention, "Tor Vergata" University of Rome, Via Montpellier 1, 00133 Rome, Italy.
Department of Orthopaedics and Traumatology, "Policlinico Tor Vergata" Foundation, Viale Oxford 81, 00133 Rome, Italy.
Biomedicines. 2024 Sep 28;12(10):2217. doi: 10.3390/biomedicines12102217.
Biological drugs, including monoclonal antibodies, represent a revolutionary strategy in all fields of medicine, offering promising results even in the treatment of osteoarthritis (OA). However, their safety and efficacy have not been fully validated, highlighting the need for in-depth studies. Therefore, we provided a comprehensive systematic review of the intra-articular use of monoclonal antibodies for the treatment of OA in animal models, reflecting ongoing efforts to advance therapeutic strategies and improve patient outcomes. A systematic literature search was conducted in December 2023 following the PRISMA guidelines, using the Web of Science, Google Scholar, and PUBMED databases. Out of a total of 456, 10 articles were included in the study analyzing intra-articular antibodies and focusing on various targets, including vascular endothelial growth factor (VEGF), nerve growth factor (NGF), interleukin 4-10 (IL4-10), tumor necrosis factor α (TNF-α), a disintegrin and metalloproteinase with thrombospondin motifs 5 (ADAMTS5), and matrix metalloproteinase 13 (MMP-13). Most studies administered the antibodies weekly, ranging from 1 to 10 injections. Animal models varied, with mean follow-up periods of 8.9 ± 4.1 weeks. The methods of assessing outcomes, including pain and morpho-functional changes, varied. Some studies reported only morphological and immunohistochemical data, while others included a quantitative analysis of protein expression. In conclusion, monoclonal antibodies represent a promising avenue in the treatment of OA, offering targeted approaches to modulate disease pathways. Further research and clinical trials are needed to validate their safety and efficacy, with the potential to revolutionize the management of OA and reduce reliance on prosthetic interventions.
生物药物,包括单克隆抗体,在医学的各个领域都代表着一种革命性的策略,即使在骨关节炎(OA)的治疗中也能带来有前景的结果。然而,它们的安全性和有效性尚未得到充分验证,这凸显了深入研究的必要性。因此,我们对单克隆抗体在动物模型中关节腔内使用治疗OA进行了全面的系统综述,反映了为推进治疗策略和改善患者预后所做的持续努力。按照PRISMA指南,于2023年12月使用科学网、谷歌学术和PubMed数据库进行了系统的文献检索。在总共456篇文献中,有10篇文章被纳入该研究,分析关节腔内抗体并聚焦于各种靶点,包括血管内皮生长因子(VEGF)、神经生长因子(NGF)、白细胞介素4 - 10(IL4 - 10)、肿瘤坏死因子α(TNF-α)、含血小板反应蛋白基序的解聚素和金属蛋白酶5(ADAMTS5)以及基质金属蛋白酶13(MMP - 13)。大多数研究每周注射抗体,注射次数从1次到10次不等。动物模型各不相同,平均随访期为8.9±4.1周。评估结果的方法,包括疼痛和形态功能变化,各不相同。一些研究仅报告了形态学和免疫组织化学数据,而其他研究则包括了蛋白质表达的定量分析。总之,单克隆抗体在OA治疗中代表着一条有前景的途径,提供了调节疾病途径的靶向方法。需要进一步的研究和临床试验来验证它们的安全性和有效性,其有可能彻底改变OA的管理方式并减少对假体干预的依赖。