CD80
免疫系统
免疫耐受
单宁酸
CD86
免疫学
关节炎
阿巴塔克普
炎症
材料科学
医学
T细胞
癌症研究
细胞毒性T细胞
化学
CD40
抗体
生物化学
体外
有机化学
美罗华
作者
Yina Wu,Jin-Won Park,Dongun Jin,Jaiwoo Lee,Quoc‐Viet Le,Yu‐Kyoung Oh
标识
DOI:10.1002/adfm.202305563
摘要
Abstract Here, a tannic acid‐based nanomaterial is developed for treating rheumatoid arthritis by inducing antigen‐specific immune tolerance. The tolerogenic nanovaccine is designed for targeted delivery of dexamethasone and citrullinated peptide in a lipid‐coated nanoparticle consisting of tannic acid as core nanomaterial (CitDTN). The surface of CitDTN is modified with abatacept to yield AbaCitDTN. Abatacept modification enables the tolerogenic nanovaccine to target dendritic cells by interacting with the co‐stimulatory molecules, CD80 and CD86. This modification increases the lymph node accumulation of the tolerogenic nanovaccine upon subcutaneous administration. In addition, AbaCitDTN reprograms the properties of dendritic cells toward tolerogenic phenotypes and interrupts co‐stimulatory signals between dendritic cells and T cells, leading to suppressed T cell proliferation and interlukin‐2 secretion. Collagen‐induced arthritis DBA/1 model mice are subcutaneously administered with AbaCitDTN weekly for a total of four injections. This reduces inflammation in the synovial space and decreases autoimmunity against type II collagen and citrullinated peptide. In vivo administration of AbaCitDTN improves clinical symptoms and protects joints from destruction in this animal model. These findings suggest that tannic acid‐based nanomaterials could have potential to induce antigen‐specific immune tolerance for treating rheumatoid arthritis.
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