类风湿性关节炎
血管生成
肿瘤坏死因子α
医学
关节炎
癌症研究
单克隆抗体
血管内皮生长因子
免疫学
炎症
体内
抗体
蛋白激酶B
磷酸化
血管内皮生长因子受体
生物
细胞生物学
生物技术
作者
Nanwen Zhang,Ningning Zheng,Dunxiong Luo,Juan Lin,Duoduo Lin,Yongkang Lu,Weipeng Lai,Yize Bian,He Wang,Jian Ye,Juhua Yang,Jiaan Liu,Wenzhong Que,Xiaole Chen
标识
DOI:10.1016/j.intimp.2023.111240
摘要
Anti-TNF-α therapy fails in 30% of patients, where TNF-α may not be the key causative factor in these patients. We developed a bispecific single-domain antibody block TNF-α and VEGF (V5-3).The experiments showed that V5-3 effectively activated proliferation and migration of RA-FLS and HUVEC, tube-forming role of HUVEC, and expression of inflammatory factors in vitro. Besides, the experiments indicated that the anti-RA activity of V5-3 was superior to Anbainuo in vivo. Application of V5-3 reduced the expression of inflammatory factors, extent of synovial inflammation and angiogenesis and attenuated the severity of autoimmune arthritis in collagen-induced arthritis (CIA) mice. Mechanistically, V5-3 suppressed p65, AKT and VEGFR2 phosphorylation, as well as production of TNF-α and VEGF in joint tissues. These results demonstrated that V5-3 displayed a superior effect of anti-RA, may be a new therapy to overcome the limitations of anti-TNF-α monoclonal antibody.
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