posted on 2022-08-18, 14:10authored byYuxuan Ma, Zhangwei Lu, Bin Jia, Ye Shi, Jun Dong, Shuoxing Jiang, Zhe Li
Rheumatoid arthritis (RA) severely threatens human health
by causing
inflammation, swelling, and pain in the joints and resulting in persistent
synovitis and irreversible joint disability. In the development of
RA, pro-inflammatory M1 macrophages, which express high levels of
reactive oxygen species (ROS) and nitric oxide (NO), induce synovial
inflammation and bone erosion. Eliminating ROS and NO in the inflamed
joints is a potential RA therapeutic approach, which can drive the
transition of pro-inflammatory M1 macrophages to the anti-inflammatory
M2 phenotype. Taking advantage of the intrinsic ROS- and NO-scavenging
capability of DNA molecules, herein, we report the development of
folic acid-modified triangular DNA origami nanostructures (FA-tDONs)
for targeted RA treatment. FA-tDONs could efficiently scavenge ROS
and NO and actively target M1 macrophages, facilitating the M1-to-M2
transition and the recovery of associated cytokines and biomarkers
to the normal level. The therapeutic efficacy of FA-tDONs was examined
in the RA mouse model. As validated by appearance, histological, and
serum examinations, FA-tDONs treatment effectively alleviated synovial
infiltration and cartilage damage, attenuating disease progression.
This study demonstrated the usage of DNA origami for RA treatment
and suggested its potential in other antioxidant therapies.