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Kidney Diseases Stem Cell Therapy Development

Kidney Diseases Stem Cell Therapy Development

Kidney disease encompasses a range of disorders affecting the kidneys' structure and function, including chronic kidney disease (CKD), acute kidney injury (AKI), and certain genetic kidney diseases. Stem cell therapy offers a potential avenue to repair or regenerate damaged kidney tissue. CD BioSciences offers stem cell therapy development services for kidney diseases, based on out advanced technology and professional team.

Fig 1. Kidney

Introduction into Kidney Diseases

Kidney diseases represent a significant health challenge globally, affecting millions of individuals and often leading to severe complications if left untreated. The kidneys play a vital role in filtering waste products and excess fluids from the blood, maintaining electrolyte balance, and regulating blood pressure. When kidney function is compromised due to disease or injury, it can result in various kidney disorders, such as chronic kidney disease (CKD), acute kidney injury (AKI), and end-stage renal disease (ESRD).

Stem Cell Therapy for Kidney Diseases

Stem cell therapy is a groundbreaking approach in regenerative medicine that holds significant potential for the treatment of kidney diseases. Stem cells, with their unique ability to differentiate into various cell types, offer several advantages for addressing kidney disorders: 1) Regeneration of Kidney Tissue; 2) Anti-Inflammatory Effects; 3) Immunomodulation; 4) Angiogenesis.

Fig 2. Mechanism of MSCs in the treatment of kidney diseasesMechanism of MSCs in the treatment of kidney diseases (Liu, et al., 2020)

The preferential transport of MSCs to sites of ischemia, hypoxia, and inflammatory response after injury plays a crucial role in the success of organ injury cell therapy. MSCs secrete a broad repertoire of cytokines, chemokines, and growth factors, including:

  • IL-6 and IL-11
  • Macrophage-colony stimulating factor (M-CSF)
  • Vascular endothelial growth factor (VEGF)
  • Granulocyte-colony stimulating factor (G-CSF)
  • Insulin-like growth factor (IGF)
  • Leukemia inhibitory factor (LIF)
  • Basic fibroblast growth factor (bFGF)
  • Monocyte-chemoattractant protein-1 (MCP-1)
  • Hepatocyte growth (HGF)

They contribute in renal protection by promoting proliferation of epithelial cells and angiogenesis, anti-apoptosis, anti-inflammatory, anti-fibrosis, and other signaling pathways. Followings are clinical trails of MSCs utilized in kidney disease treatment.

Condition or disease Source Main findings
AKI after cardiac surgery Allogeneic BM-MSCs
  • MSC infusion was safe
  • None of the patients developed postoperative AKI or subsequent loss of kidney function
  • Protection against early and late post-surgery kidney function deterioration
  • Reduction in length of hospital stay
  • No significant difference between groups in 30-d all-cause mortality or dialysis
  • No reduction in the time to recover kidney function
CKD Autologous BM-MSCs
  • MSC infusion was safe and tolerated
  • No significant changes in eGFR and SCr
Autologous AD-MSCs
  • MSC infusion was safe and not associated with adverse effects
  • Statistically significant improvement in urinary protein excretion but not in GFR
Autologous CD34+ EPCs
  • MSC infusion was safe and tolerated
  • No additional benefit from EPCs up to a follow-up period
  • Significantly lower unfavourable clinical outcomes (dialysis or death) in treatment group
Diabetic nephropathy (type 2) Allogeneic BM-MSCs
  • MSC infusion was safe and not associated with acute adverse events
  • Stabilization and improvement in eGFR and mGFR
Atherosclerotic renovascular disease Autologous AD-MSCs
  • MSC infusion was safe and well tolerated.
  • Increment in cortical perfusion and renal blood flow
  • Reduction in renal tissue hypoxia within poststenotic kidney
Refractory SLE Allogeneic BM-MSCs
  • MSC infusion was safe and well-tolerated
  • It improved disease activity and stabilized kidney function
  • MSC infusion was safe
  • It also reduced protein in the urine at 9- and 12-month follow-ups
LN (class III or IV) Allogeneic UC-MSCs
  • No apparent additional effect over and above standard immunosuppression
Active and refractory LN Allogeneic BM-MSCs or UC-MSCs
  • Significant improvement in proteinuria levels during the 1st month after treatment
  • The ameliorations were sustained throughout the follow-up period
Kidney transplant Autologous BM-MSCs
  • MSC infusion was safe and didn't harm kidney transplant survival
  • It lowered the chances of kidney rejection
  • It reduced the risk of infections and improved kidney function after 1 year
  • It boosted the immune system's helpful T cells and controlled harmful memory T cells
  • There were no major side effects in the long term

Our Services

CD BioSciences offers stem cell therapy development service for spinal cord injury based on our advanced technology and professional team. Our stem cell therapy development services are offered in kidney diseases included but not limited as follows:

  • Diabetic Nephropathy
  • Lupus Nephritis
  • Hypertensive Nephropathy
  • Kidney Transplantation

As a pioneer in biotechnology, CD BioSciences has grown into one of the largest independent biotechnology companies in the world. CD BioSciences is committed to providing professional and efficient service to our customers around the world. If you are interested in our service, please contact us.

Reference

  1. Liu, D., Cheng, F., Pan, S. et al. Stem cells: a potential treatment option for kidney diseases. Stem Cell Res Ther 11, 249 (2020).

For research use only, not for clinical use.