Evaluating The Immunomodulatory Effects of High Dose Intravenous Administration of Allogeneic Umbilical Cord-Derived Mesenchymal Stem Cells

Evaluating The Immunomodulatory Effects of High Dose Intravenous Administration of Allogeneic Umbilical Cord-Derived Mesenchymal Stem Cells

Mesenchymal stem cells (MSCs) are multipotent fibroblast-like cells found throughout the body and have been found to have self-renewing and multilinear therapeutic potential by providing new cells for tissue repair by replacing damaged cells. 

Thought to stimulate repair and control the immune response through an expression of growth factors and other cytokines, MSCs are at low risk of rejection and repair tissue damage through immunomodulation, not by their ability to differentiate.  

While MSCs can be isolated from a number of tissue sources, including bone marrow, peripheral blood, adipose (fat) tissue, umbilical cord blood, and umbilical cord tissue (Wharton’s jelly). MSCs derived from the human umbilical cords (UCMSCs) have been found to have significant advantages over MSCs isolated from other sources. These advantages include higher proliferation and self-renewal capacity and multilineage differentiation capability.  

Unlike many sources of MSCs, the umbilical cord is considered medical waste, making the collection of UCMSCs noninvasive and eliminating ethical concerns associated with the collection of MSCs from other sources. These UCMSCs have been developed as effective “off-the-shelf” cell therapy for a number of conditions, including autoimmune diseases, and as a treatment for a number of emergency medical conditions. 

This Phase 1 clinical study, designed and conducted by Chin et al., intended to determine the safety and efficacy of intravenous allogeneic infusion of UCMSCs in healthy volunteers and to determine the effective dose at which an immunomodulatory effect is observed. The findings of this study are intended to serve as a guideline and benchmark for future CVL-100 clinical research. 

Analyzing the results of this clinical study, the authors report that there was no observed complication resulting from the infusion and no significant adverse event in either dosage group in the 6 months of follow-up. These findings led Chin et al. to conclude that UCMSCs infusion was safe among healthy subjects, results that were consistent with other UCMSC treatment-based studies.


The authors also reported that UCMSCs infusion posed no significant adverse effects in patients with type 2 diabetes. Despite the relatively small sample group of this study (11 subjects), the authors reported demonstrating an initial transient proinflammatory effect followed by a significant and prolonged anti-inflammatory effect.

In addition, Chin et al. report found that high-dose (HD) CLV-1000 infusion provided a significant increase in both hemoglobin level and MCV level that falls within the normal range.  Biomarker assessment results also indicated that the HD group demonstrated a significant steady increase of cytokine IL-1RA from baseline up until 6 months of posttreatment. This finding is especially important as IL-1RA is a naturally occurring antagonist to the proinflammatory cytokine 1L-1.

The authors conclude that this study clearly demonstrates a difference in immunomodulatory effect between the high-dose and low-dose treatment groups, with the HD group demonstrating a significantly greater reduction of proinflammatory cytokine TNF-α and an increased level of specific anti-inflammatory cytokines within 6 months and in relation to those in the low dose group. Considering this, Chin et al. conclude that a CLV-100 dosage of two million MSCs per kilogram of body weight represents the optimal dose level for overcoming inflammatory conditions by displaying the best improvement in all parameters tested, absence of side effects, and SAEs.

The data collected in this study also suggests that this is the first study to report a significant reduction of globulin observed over the course of the study. This is important because globulin serves an important role in immunity. Additionally, increases in serum globulins are associated with several immune-mediated diseases, including rheumatoid arthritis, chronic liver disease, diabetes mellitus, and cancer.

Considering these findings, the authors of this study conclude that high doses of allogeneic MSCs could help exert beneficial effects of repair and healing. 

Source:  “High Dose of Intravenous Allogeneic Umbilical Cord-Derived ….” https://www.hindawi.com/journals/sci/2020/8877003/

What Are Peptides?

What Are Peptides?

Peptides can be beneficial for your general wellness. They exist naturally within your body, but they can also be administered through regenerative treatments. 

What are these compounds, and how can they be used in regenerative medicine?

Peptides Are Strings of Amino Acids

Peptides are made of amino acids, the chemical building blocks for proteins. Your body makes and uses many different peptides for different purposes. 

Some peptides generate beneficial tissues and compounds, like collagen or creatine. Others work through medications to combat certain health conditions, such as diabetes

Peptides can boost your health and well-being in many ways when used in regenerative treatments. 

Creatine Peptides for Muscle Growth 

Creatine peptides may boost muscle growth and strength over time. These muscle-building peptides can be used in treatments that aim to alleviate musculoskeletal pain. 

When your muscle fibers break down and are not repaired properly, you can experience pain, discomfort, and loss of mobility. Peptides can reinforce the structure and strength of your muscles to help you regain comfort and mobility. 

Collagen Peptides for Skin and Hair Rejuvenation

Many supplements contain collagen peptides, which are believed to enhance the skin barrier. Collagen is a skin fiber that keeps your skin firm, elastic, and resistant to impact. As you get older, your body produces less collagen, and your skin starts to age. 

With collagen peptides, your body can repair and reinforce your skin barrier to give you a more youthful appearance. They can also slow the skin aging process by giving your body the building blocks to make more collagen. 

Collagen peptides can also enhance your hair health. If you struggle with hair loss and balding, collagen peptides could make a noticeable difference. Collagen fibers add strength and structure to your hair for enhanced growth. 

Peptides for Joint Recovery 

Joint health is important for mobility, comfort, and quality of life. Certain peptides may aid in joint recovery and regeneration to ease the painful symptoms of some joint problems. 

When you lose cushioning around your joints due to tissue degeneration, you might experience pain and stiffness in these areas. Certain peptides may help rebuild these tissues to make movement and functioning easier and more comfortable. 

Combined with stem cell therapy, peptides could reduce inflammation around your joints to give you a better quality of life. 

Regenerative Medicine: Peptides for Healing and Relief

Regenerative medicine uses the power of peptides and other compounds to potentially manage symptoms and relieve pain. If you struggle with chronic health problems, this could be a game changer for your daily functioning and comfort levels. 

Contact Stemedix today to learn more

Mesenchymal Stem Cells and Osteoarthritis

Mesenchymal Stem Cells and Osteoarthritis

Osteoarthritis (OA) is the most common form of arthritis and affects an estimated 25% of adults in the United States. Characterized by pain, stiffness, and inflammation in the joints of the body, OA is most frequently observed in the knees, hands, hips, and spine.

OA is one of the leading causes of disability with an annual cost of medical care and lost earnings exceeding $300 billion. With over 250 million people affected by OA worldwide, the combination of aging, obesity, and increased incidents of oxidative stress is causing the condition to become increasingly prevalent.

To date, treatment and medical interventions – including exercise, physical therapy, lifestyle modifications, and prescription and over-the-counter medications – have been successful in managing symptoms, reducing pain, and maintaining joint mobility, but have not been able to promote the regeneration of degenerated tissue.

Stem cells, and specifically mesenchymal stem cells (MSCs), have been identified as a potential therapy option for OA. In this review, Zhu et al. summarize the pathogenesis and treatment of OA and review the current status of MSCs as a potential treatment option for the condition.

In reviewing the pathogenesis of OA, the authors highlighted the fact that OA is a dynamic and progressive degenerative disease that is primarily caused by the imbalance between restoration and destruction of the joints; the disease is also significantly influenced by environmental, inflammatory, and metabolic aspects.

The authors highlight that the primary goals of current OA treatment methods are to reduce pain, slow progression, and preserve and improve joint mobility and function.

As researchers continue to search for therapies that encourage the regeneration of damaged articular cartilage and the alleviation of inflammation, they’ve turned their attention to a number of stem cell-based therapies, such as autologous chondrocyte implantation (ACI).  While ACI has received FDA approval, unexpected dedifferentiation, and joint invasiveness during harvest limit the availability and usefulness of this application.  

Fortunately, MSCs have not been found to demonstrate limitations similar to those observed in ACI and are considered novel therapeutic agents for the treatment of OA. Prized primarily for their ability to stimulate cartilage formation and for their vascularization, anti-inflammation, and immunoregulation, MSCs are sourced from different types of stem cells, including bone marrow  (BM-MSCs), adipose tissue (AD-MSCs), and umbilical cord (UC-MSCs). Zhu et al. summarize the characteristics, advantages, and disadvantages of each of these MSC sources in this review.

The authors point out that several clinical trials have proven both the safety and potential efficacy of BM-MSCs, AD-MSCs, and UC-MSCs in the treatment of OA.  However, the authors also point out that several of these trials were conducted with limited samples, without rigorous controls, and with relatively short-term follow-up. Considering this, Zhu et al. call for additional clinical trials using larger samples, more rigorous controls, and additional long-term follow-up. In addition, the authors also call for additional considerations to further enhance the efficacy in clinical trials, including cell density, time and location for MSC transplantation, and pretreatment of MSCs by inflammatory cytokines.

The authors conclude that while stem cell-based therapy, and specifically MSCs, demonstrate great potential for the regeneration of new cartilage and strong immunoregulatory capacity, the identified limitations and risks of MSC-based therapy should be realized and treated carefully.  

Despite the identified risks and limitations, MSC-based therapy for the treatment of OA might achieve better efficacy in regenerative medicine, especially when administered in combination with other treatment options.

Source: “Mesenchymal stem cells in osteoarthritis therapy: a review – NCBI.” 15 Feb. 2021, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868850/

A Review of Circulating Mesenchymal Stem Cells

A Review of Circulating Mesenchymal Stem Cells

Mesenchymal stem cells (MSCs) have been widely used in a number of applications designed to aid in the regeneration and healing of human tissue. Prized for their multipotent capacity to differentiate into a variety of other specific cell types, MSCs have consistently demonstrated the ability to seek out damaged tissue while also reducing inflammation and promoting healing.

Recently, the discovery of a specific type of MSC known as circulating mesenchymal stem cells has demonstrated increased potential for the use of MSCs in the regeneration, repair, and engineering of tissue throughout the body.  

Circulating MSCs demonstrate characteristics similar to MSCs that are derived from bone marrow and are typically found in very low concentrations in healthy individuals. While these specific MSCs have demonstrated the ability to migrate to the site of damaged or injured tissue like other MSCs, what makes circulating MSCs so interesting to researchers is their distinct genetic profile – especially when compared to bone marrow-derived stem cells (BM-MSCs).

Xu and Li’s review provides a summary of the basic knowledge of circulating MSCs, their potential clinical applications, and the issues of using allogeneic MSCs for clinical therapy.

While these circulating MSCs, also known as peripheral blood-derived MSCs (PB-MSCs), have great potential in the field of tissue engineering and regeneration, they are found in very low quantities within the human body. As a point of reference, Xu and Li point out that the frequency of BM-MSCs in humans under normal conditions is very low and ranges from 1 in 104 to 1 in 105.  Compared to BM-MSCs, the concentration of circulating MSCs is even lower, typically around 1 in 108.

Despite their low numbers, researchers have successfully identified and collected PB-MSCs in both animal and human models. In both scenarios, PB-MSCs demonstrated characteristics of cell proliferation and multi-differentiation potential that are similar to those observed in BM-MSCs.  In addition, and adding to their potential, PB-MSCs are plastic-adherent, have multi-differentiation potential, and demonstrate the ability to differentiate into a variety of cells. 

Adding to the benefits described above, and unlike stem cells harvested from embryonic sources, PB-MSCs are not attached to ethical concerns. In addition, numerous research studies have demonstrated the use of MSCs in a variety of applications, including cardiovascular, bone, and cartilage repair have resulted in general significant improvements in tissue healing and regeneration. 

To date, studies specific to circulating MSCs are rare. However, Xu and Li highlight that circulating MSCs, while originally found in the bone marrow and other sources throughout the body, are a special subset of MSCs found in circulation. While additional study is required, early research seems to indicate that the release of these circulating MSCs is tightly controlled by a variety of systematic and local factors, including inflammatory cytokines, hormones, and a variety of growth factors. 

There is increasing evidence that indicates MSCs are immunosuppressive cells and that allogeneic MSCs may be used with similar therapeutic efficacy to autologous MSCs. Considering this, Xu and Li conclude that allogeneic transplantation seems to be more promising and a way to ensure that patients can receive treatment at the best time and without significant fear of rejection. 

As research continues to explore the potential benefits and drawbacks of circulation MSCs, the authors point out that a lack of standard procedures for therapeutic MSC administration remains a critical issue for the clinical application of MSCs. These critical issues need to be addressed through carefully designed animal and clinical trials before clinical applications of MSCs can be used in patients with certain diseases.

Source:  “Circulating mesenchymal stem cells and their clinical implications.” https://www.sciencedirect.com/science/article/pii/S2214031X1300048X

Regenerative Medicine for Ankle Pain Relief

Regenerative Medicine for Ankle Pain Relief

Regenerative medicine, also known as stem cell therapy, is an alternative medicine that seeks to replace damaged tissue and/or organs. Usually, this damage is a result of disease, congenital issues, or trauma. Regenerative therapies are distinct from clinical strategies. Typically, clinical strategies primarily focus on treating the symptoms of an issue. Regenerative therapies, on the other hand, seek to address the issue itself. Here we will discuss Regenerative Medicine for ankle pain.

In recent years and based on research, stem cell therapy has become a more often explored option either in conjunction with traditional medicine or if options have been exhausted. It can be used to help manage and potentially provide a healing cascade for joint pain associated with certain injuries and illnesses.

What Are Stem Cells?

Stem cells are raw materials in the body. They’re the cells from which other specialized cells are generated. Stem cells will divide to form more cells, which are called daughter cells. Daughter cells transform into either new stem cells or specialized cells that perform a more specific function. Some of these specialized cells include:

  • Brain cells
  • Blood cells
  • Bone cells
  • Heart muscle cells

Mesenchymal stem cells are fascinating because no other cell in the human body has the ability to generate completely new cell types.

What Is Stem Cell Therapy?

Stem cell therapy uses stem cells to help repair injured, dysfunctional, or diseased tissue. Using stem cells in medicine can help support your body’s ability to heal and regenerate itself while reducing pain.

Common Causes of Ankle Pain

Some common injuries associated with ankle pain include:

  • Achilles tendon rupture
  • Achilles tendinitis
  • Avulsion fracture

Sometimes, ankle pain can happen without an injury, as in the case of rheumatoid arthritis, gout, osteoarthritis, and lupus.

Stem Cell Therapy for Ankle Pain

Since stem cell therapy has dual functions (i.e., the healing function and the pain relief function), stem cell therapy can manage ankle pain that is or isn’t associated with injuries.

Patients’ response to therapy may vary on when they see potential improvements, but generally they may experience some pain relief after around three weeks post-treatment. This improvement will gradually continue over the course of months or years.

Benefits of Regenerative Medicine

Depending on the degree of injury, stem cells have the ability to help regenerate the injured or diseased tissues. For patients who want to avoid invasive surgeries or pain medications to address their musculoskeletal injury, stem cell therapy may be an option to explore. This post was written by a medical professional at Stemedix Inc. At Stemedix we provide access to Regenerative Medicine for Orthopedic also known as Orthopedic Stem cell Therapy. Regenerative medicine has the natural potential to help improve symptoms sometimes lost from the progression of many conditions. If you want to learn more about Regenerative Medicine for ankle pain, contact us today at Stemedix.

Regenerative Medicine For Alzheimer’s Disease

Regenerative Medicine For Alzheimer’s Disease

Alzheimer’s disease (AD) is the most common cause of dementia, accounting for an estimated 50%-70% of dementia cases worldwide.  Characterized by memory loss and cognitive impairment, AD is progressive, debilitating, and fatal.  In addition, it’s estimated that new cases of AD around the globe are occurring at a staggering rate of 20 per minute with an established effective treatment yet to be discovered.

To date, research has demonstrated an advanced understanding of AD’s development and devastating – and eventually fatal – outcomes, but has only been able to identify drugs that intervene too late in the progression of the condition.

Considering that stem cells have a detailed and documented record of their ability of self-renewal, proliferation, differentiation, and transformation into different types of central nervous system neurons and glial cells and that they have been successful in AD animal models, it is believed that stem cells have the potential to treat patients with AD.  

In reviewing the progress of stem cells as a potential therapeutic treatment for AD, Liu et al. call for new treatments, including the removal of toxic deposits and the ability to replace lost neurons to be developed and as a way to stimulate neural precursors, prevent nerve death, and enhance structural neural plasticity.  The authors also review the pathophysiology of AD and the application prospect of related stem cells based on specific cell types.

Liu et al. point out that, although AD models using animal research have been demonstrated to be successful, animal research is difficult to translate into human trials, and, to date, none have been able to replicate the complex environment observed in the human brain.  Considering this, the authors conclude that it is challenging, at best, to characterize the beneficial effects of stem cells in AD based solely on previously conducted animal models. 

As a result of this review, the authors also conclude that while stem cells used in AD and animal models have achieved certain results, there are still several factors that require consideration.  Among these factors is the fact that this type of stem cell therapy requires neurosurgical procedure and immunosuppression which contributes to ongoing concerns related to controlling the proliferation and differentiation of stem cells, the targeting of molecular markers, and the development of cell delivery systems.  

The authors acknowledge that progression in the study of stem cells in AD applications should be made more efficient because of recent technological advances in stem cells, specifically using hydrogels, nano-technology, and light therapies to produce more efficient delivery of treatment.

While these advances should help, Liu et al. also point out that a number of obstacles, including uncertainty about the amyloid hypothesis, differing objectives related to preventing progression vs symptomatic treatment, and demonstrating the relationship between stem cell treatment and complete AD cure, still need to be addressed.

Considering the findings of this review, the authors conclude that stem cell therapy for AD carries enormous promise, but the successful application will most likely be dependent upon consistent early diagnosis of the condition in order to prevent further brain cell deterioration and will likely be combined with an administration of existing medication as a way to most effectively treat and/or prevent AD.

Source: Mesenchymal stem cell-based therapy for autoimmune diseases.” https://pubmed.ncbi.nlm.nih.gov/30623280/.

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