Cell-free DNA depletion via cell-penetrating poly(disulfide)s for rheumatoid arthritis therapy

2022 ◽  
Vol 26 ◽  
pp. 101351
Author(s):  
Wenbo Geng ◽  
Maowen Chen ◽  
Bailong Tao ◽  
Rong Wang ◽  
Dong Wang ◽  
...  
2015 ◽  
Vol 6 (1-2) ◽  
pp. 23-30 ◽  
Author(s):  
Marina Dunaeva ◽  
Bastiaan C. Buddingh’ ◽  
René E. M. Toes ◽  
Jolanda J. Luime ◽  
Erik Lubberts ◽  
...  

2007 ◽  
Vol 53 (9) ◽  
pp. 1609-1614 ◽  
Author(s):  
Xiao-Yan Zhong ◽  
Ines von Mühlenen ◽  
Ying Li ◽  
Anjeung Kang ◽  
Anurag Kumar Gupta ◽  
...  

Abstract Background: Increased concentrations of cell-free DNA have been found in several disorders and have been interpreted as evidence of increased rates of cell death or turnover. Evidence from in vitro and animal experiments suggests that DNA may play a role in the pathogenesis of rheumatoid arthritis (RA). Methods: We measured cell-free DNA in plasma and serum from patients with RA and healthy controls by use of quantitative PCR for glyceraldehyde-3-phosphate dehydrogenase (GAPDH) DNA. We used protein G Sepharose™ bead adsorption of plasma and elution to isolate antibody-bound DNA. Results: In paired plasma and serum samples of 16 healthy controls the median GAPDH copies were 4500 genome equivalents (GE)/mL plasma (range 319–21 000) and in 26 RA patients 17 000 GE/mL plasma (2100–2 375 000, P = 0.0001). In the serum from normal controls the median GAPDH copies were 35 000 GE/mL (1700–239 000) and from RA patients 222 000 GE/mL (21 000–2 375 000, P = 0.004). A median of 81% of the cell-free DNA in RA was associated with antibody compared with 9% in healthy controls (P = 0.001). The concentrations of DNA did not vary with the type of therapy patients received. Conclusions: These results provide new evidence for a role of cell-free DNA-antibody complexes in the etiology of RA, suggest new avenues for basic research, and may prove to be relevant to diagnosis and assessment of therapy.


Author(s):  
Vanda Mlynarikova ◽  
Frantisek Malis ◽  
Peter Celec ◽  
Barbora Vlkova ◽  
Emoke Stenova

2021 ◽  
Vol 22 (16) ◽  
pp. 8941 ◽  
Author(s):  
Teppei Hashimoto ◽  
Kohsuke Yoshida ◽  
Akira Hashiramoto ◽  
Kiyoshi Matsui

Endogenous DNA derived from the nuclei or mitochondria is released into the bloodstream following cell damage or death. Extracellular DNA, called cell-free DNA (cfDNA), is associated with various pathological conditions. Recently, multiple aspects of cfDNA have been assessed, including cfDNA levels, integrity, methylation, and mutations. Rheumatoid arthritis (RA) is the most common form of autoimmune arthritis, and treatment of RA has highly varied outcomes. cfDNA in patients with RA is elevated in peripheral blood and synovial fluid and is associated with disease activity. Profiling of cfDNA in patients with RA may then be utilized in various aspects of clinical practice, such as the prediction of prognosis and treatment responses; monitoring disease state; and as a diagnostic marker. In this review, we discuss cfDNA in patients with RA, particularly the sources of cfDNA and the correlation of cfDNA with RA pathogenesis. We also highlight the potential of analyzing cfDNA profiles to guide individualized treatment approaches for RA.


2016 ◽  
Vol 20 (6) ◽  
pp. 722-730 ◽  
Author(s):  
Teppei Hashimoto ◽  
Kohsuke Yoshida ◽  
Naonori Hashimoto ◽  
Ayako Nakai ◽  
Kenta Kaneshiro ◽  
...  

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