High-Tech Methods of Cytokine Imbalance Correction in Intervertebral Disc Degeneration.
Natalya A ShnayderAzamat V AshhotovVera V TrefilovaMaxim A NovitskyGerman V MedvedevMarina M PetrovaEkaterina A NarodovaDaria S KaskaevaGalina A ChumakovaNatalia P GarganeevaNatalia V LarevaMustafa Al-ZamilAzat R AsadullinRegina F NasyrovaPublished in: International journal of molecular sciences (2023)
An important mechanism for the development of intervertebral disc degeneration (IDD) is an imbalance between anti-inflammatory and pro-inflammatory cytokines. Therapeutic and non-therapeutic approaches for cytokine imbalance correction in IDD either do not give the expected result, or give a short period of time. This explains the relevance of high-tech medical care, which is part of specialized care and includes the use of new resource-intensive methods of treatment with proven effectiveness. The aim of the review is to update knowledge about new high-tech methods based on cytokine imbalance correction in IDD. It demonstrates promise of new approaches to IDD management in patients resistant to previously used therapies, including: cell therapy (stem cell implantation, implantation of autologous cultured cells, and tissue engineering); genetic technologies (gene modifications, microRNA, and molecular inducers of IDD); technologies for influencing the inflammatory cascade in intervertebral discs mediated by abnormal activation of inflammasomes; senolytics; exosomal therapy; and other factors (hypoxia-induced factors; lysyl oxidase; corticostatin; etc.).
Keyphrases
- cell therapy
- stem cells
- anti inflammatory
- tissue engineering
- healthcare
- end stage renal disease
- palliative care
- induced apoptosis
- randomized controlled trial
- systematic review
- mesenchymal stem cells
- chronic kidney disease
- genome wide
- ejection fraction
- oxidative stress
- copy number
- peritoneal dialysis
- bone marrow
- prognostic factors
- big data
- machine learning
- cell cycle arrest
- pain management
- deep learning
- chronic pain
- cell proliferation
- transcription factor
- pi k akt