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DNA extracellular traps as potential biomarker of chronic haemophilic synovitis and therapeutic perspective in patients treated with PRP

P. Oneto1, M. Landro2, C. Daffunchio2, A. Douglas Price3, E. Carrera SIlva1, H. Caviglia2, J. Etulain4

1IMEX-ANM-CONICET, Buenos Aires, Ciudad Autonoma de Buenos Aires, Argentina, 2Department of Orthopedic Surgery and Traumatology, Dr. Juan A. Fernández Hospital, Buenos Aires, Ciudad Autonoma de Buenos Aires, Argentina, 3Department of Orthopedic Surgery and Traumatology, Dr. Juan A. Fernández Hospital, Buenos aires, Ciudad Autonoma de Buenos Aires, Argentina, 4IMEX-ANM-CONICET, Buenos Aires, Cordoba, Argentina

Abstract Number: PB0191

Meeting: ISTH 2022 Congress

Theme: Hemophilia and Rare Bleeding Disorders » Hemophilia - Basic

Background: Haemophilia-associated hemarthrosis cause chronic haemophilic synovitis (CHS). Although neutrophils are major immune blood cells infiltrating joints after bleeding, their role on the pathogenesis of CHS is unknown. Neutrophils release extracellular DNA traps (ETs), structures of DNA with bound granular enzymes (including elastase) that were associated with tissue damage.

Aims: To evaluate the presence of ETs as pathogenic biomarkers, and the protective effect of intraarticular injection of platelet-rich plasma (PRP) in patients with CHS.

Methods: Synovial fluids (SF) and plasma/PRP were obtained from 21 patients with CHS (28±11 years old, 19 type A, 2 type B). 22 joints (1 ankle and 21 knees) were evaluated for Hemophilia Joint Health Score (HJHS). Synovial and plasmatic ETs were indirectly quantified by fluorometry (DNA) and directly by ELISA (DNA-Elastase complexes). Pearson or Spearman correlations with clinical parameters were calculated.

Results: DNA (0.37±0.06μg/ml) and DNA-Elastase (0.27±0.03OD) were detected in SF of patients with CHS and positively correlated with HJHS (r>0.5-0.7, p < 0.05).

While DNA or DNA-Elastase were not detected in plasma of healthy donors, they were found in the plasma of CHS patients (DNA=0.17±0.01μg/ml; DNA-Elastase=0.16±0.03OD) and showed a strong positive correlation (r=0.7-0.8, p>0.05) with the synovial levels of both parameters.

Remaining ETs-inducer factors were present in SF, as this fluid induced the in vitro release of ETs from blood-isolated neutrophils. This phenomenon was impaired by adding plasma or PRP. Finally, promising preliminary data with 5 patients with CHS indicate that levels of DNA-Elastase and joint damage decreased after 2 weeks of receiving intra-articular injection of PRP.

Conclusion(s): The synovial and plasma levels of DNA-Elastase correlated with joint damage suggesting that ETs formation could be a biomarker and potential therapeutic target for CHS. The intraarticular injection of PRP underlined a new potential alternative therapy, decreasing ETs formation in synovia of patients with CHS.

Image

Figure 1. ETs were detected in SF of patients with CHS -60X, scale bar 20µm-.

Image

Figure 2. SF of CHS patients induce the release of ETs and this was impared in presence of PRP or PPP -60X, scale bar 20µm-.

To cite this abstract in AMA style:

Oneto P, Landro M, Daffunchio C, Douglas Price A, Carrera SIlva E, Caviglia H, Etulain J. DNA extracellular traps as potential biomarker of chronic haemophilic synovitis and therapeutic perspective in patients treated with PRP [abstract]. https://abstracts.isth.org/abstract/dna-extracellular-traps-as-potential-biomarker-of-chronic-haemophilic-synovitis-and-therapeutic-perspective-in-patients-treated-with-prp/. Accessed October 1, 2023.

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