Extracellular Vesicles from Mesenchymal Stromal Cells for the Treatment of Inflammation-Related Conditions.
Sean T RyanElham Hosseini-BeheshtiDinara AfroseXianting DingBinbin XiaGeorges E GrauChristopher B LittleLana McClementsJiao Jiao LiPublished in: International journal of molecular sciences (2021)
Over the past two decades, mesenchymal stromal cells (MSCs) have demonstrated great potential in the treatment of inflammation-related conditions. Numerous early stage clinical trials have suggested that this treatment strategy has potential to lead to significant improvements in clinical outcomes. While promising, there remain substantial regulatory hurdles, safety concerns, and logistical issues that need to be addressed before cell-based treatments can have widespread clinical impact. These drawbacks, along with research aimed at elucidating the mechanisms by which MSCs exert their therapeutic effects, have inspired the development of extracellular vesicles (EVs) as anti-inflammatory therapeutic agents. The use of MSC-derived EVs for treating inflammation-related conditions has shown therapeutic potential in both in vitro and small animal studies. This review will explore the current research landscape pertaining to the use of MSC-derived EVs as anti-inflammatory and pro-regenerative agents in a range of inflammation-related conditions: osteoarthritis, rheumatoid arthritis, Alzheimer's disease, cardiovascular disease, and preeclampsia. Along with this, the mechanisms by which MSC-derived EVs exert their beneficial effects on the damaged or degenerative tissues will be reviewed, giving insight into their therapeutic potential. Challenges and future perspectives on the use of MSC-derived EVs for the treatment of inflammation-related conditions will be discussed.
Keyphrases
- oxidative stress
- rheumatoid arthritis
- early stage
- anti inflammatory
- clinical trial
- cardiovascular disease
- mesenchymal stem cells
- stem cells
- bone marrow
- type diabetes
- squamous cell carcinoma
- single cell
- metabolic syndrome
- radiation therapy
- cell therapy
- cognitive decline
- climate change
- combination therapy
- early onset
- neoadjuvant chemotherapy
- systemic lupus erythematosus
- open label
- ankylosing spondylitis
- cardiovascular risk factors
- replacement therapy