Long COVID & COVID Vaccine Injury

Exploring the Potential of Mesenchymal Stem Cells in

Long COVID and COVID Vaccine Injury

There’s no arguing that the COVID-19 pandemic dealt a tsunami-like blow to all of humanity. Death, disability, lockdown, job loss, economic collapse – and that was just the first two years. Following was a rise in depression, drug overdoses, alcoholism, and domestic abuse. Suicide rates among our young people were at an all-time high, children were left in devastating educational lapse, their families in poverty, homelessness… the destruction touched everyone. For a time, cases of mild infection and the promise of life-saving vaccination provided hope that the whole nightmare might soon come to an end. Sadly, even those often came with a heavy price. As we began to dig out from beneath the rubble, two new seemingly insurmountable catastrophes emerged:

 

Vaccine Injuries & Long COVID.

 

Fatigue, shortness of breath, heart palpitations, cognitive issues and joint pain are common manifestations, but more than 200 symptoms have been identified affecting multiple organ systems. It is estimated that at least 10% of severe COVID infections result in persistent debilitation. Further, research suggests similarities with other viral-onset illnesses including ME/CFS (myalgic encephalomylelitis/chronic fatigue syndrome) and POTS/dysautonomia (postural orthstatic tachycardia syndrome). Current treatments often provide limited if any relief. Patients with severe initial infection seem to be at the highest risk for developing long COVID, but interestingly, even those who reported mild initial infection went on to develop severe long COVID symptoms. “Many people have reported [COVID vaccine] side effects—such as headache, fatigue, and soreness at the injection site—that are generally mild to moderate and go away within a few days.” –Centers for Disease Control.

Vaccine injury can look similar to long COVID but is often far worse. Injuries can manifest as chronic neuropathic pain, brain fog, the onset of new autoimmune disease, rare cancers, clotting disorders, dysautonomia, and in tragic cases, even sudden death. Research is underway, but physicians and scientists are still puzzled as to the exact mechanism of action for vaccine injuries.

Vaccine related heart damage is particularly worrisome. Cardiac tissue is unique in that it is the only tissue in the body that cannot repair itself following injury. As such, myocarditis should never be dismissed as ‘mild’. A dead heart cell stays dead then progresses to scar formation. Scarring of cardiac tissue can forever disrupt the electrical circuitry responsible for normal cardiac function. This can not be restored. Loss of life expectancy following any case of myocarditis is real and significant. Recent data reports a staggering percent of recipients had asymptomatic heart injuries following vaccination. The damage was only detected on blood and EKG testing – meaning, many people with damaged cardiac tissue are walking around without any idea whatsoever of what might lie ahead.

The healthcare community now faces the challenging task of managing these novel disease states – ones that are somehow caused by or seemingly associated with exposure to the novel spike protein. I believe that to effectively address long COVID symptoms and mitigate vaccine injuries, a paradigm shift towards therapies that harness the body’s own self-repair mechanisms is essential. One such process that holds promise is “autophagy,” which is the body’s innate repair mechanism. Fasting, intermittent fasting, exposure to temperature extremes (ice bath, infrared sauna), resveratrol, metformin, and rapalogs, are all therapies that can promote the body’s self-healing process. By doing so, these treatments clear out damaged and senescent cells, repair intracellular machinery, and restore normal physiological functioning. Another crucial aspect of damage control is immune system modulation. Immunomodulatory therapies such as vitamin D, low dose naltrexone (LDN), and thymic peptides, have shown success in restoring proper immune system function. Recently, a novel intervention has emerged that has demonstrated the potential to do both upregulate autophagy and optimize immune system function: Mesenchymal stem cell therapy (MSCs).

What Are MSCs & How Do They Work MSCs were first discovered and characterized by Dr. Arnold Caplan, a Professor of Biology and the Director of the Skeletal Research Center at Case Western University in Cleveland, Ohio. Mesenchymal stem cells are multi-potent stem cells capable of differentiating into various cell types, including bone, cartilage, and fat cells. Since his original publications, Dr. Caplan stated he wished he would have named these cells ‘medicinal signaling cells’ instead of ‘mesechymal stem cells’, because it was that it was their cell to cell signaling – and not their differentiation capabilities – that drove their regenerative properties. In the lab, MSCs can be manipulated into specific cell lines, but when introduced to a broken human body, they seek out any damaged tissues and get to work on directing repair pathways. Furthermore, MSCs exhibit potent immunomodulatory properties, which makes them a promising candidate for treating inflammatory diseases such as long COVID and vaccine injury. In essence, MSCs teach the body how to fix itself.

Stem Cells 101 Generally speaking, there are two different types of stem cells: embryonic stem cells and adult stem cells. Let’s just get this issue out of the way first – embryonic stem cells are 100% unethical to use for regenerative purposes, 100% too undifferentiated to work for this indication, and 100% ineffective for regenerative medicine purposes. I have never even seen an embryonic stem cell. Let’s move on.

In the category of adult stem cells there are two kinds:

HSCs: ‘hematopoietic stem cells’ (ie those cells used for cord blood banking and bone marrow transplantation)

MSCs: ‘mesenchymal stem cells’ (ie those that repair skeletal tissues, cartilage, bone and bone marrow fat)

HSCs are not used for regenerative purposes – it is the MSCs that do the heavy lifting, so from here on out, we’ll just be talking about these.

Where Do MSCs Come From? MSCs are kind of like your in-laws (not you, Ellen.). You can run into them just about anywhere – but only in small numbers. From a practical standpoint, high concentration MSCs are only found in in a few places: bone marrow, adipose or fat tissue, and postnatal or placental tissue. Placental tissue is just what you think it is – the tissue that is normally discarded following a live birth. When used for regenerative purposes, this tissue has to pass a rigorous screening process. Donors are all live, cesarian section births from non-vaccinated mothers.

For regenerative purposes, you can use your own stem cells (autologous) or someone else’s (allogeneic).

 

Autologous Stem Cells
You can certainly use your own stem cells, and many providers do. First, they need to be harvested using liposuction or a bone marrow biopsy – and they come out looking pretty much like what’s in those syringes. (Gross – I’m not a fan).

In addition to the painful procedure and unrefined product, there are a few other issues here. One is that as an adult, you don’t have many healthy stem cells left, and the ones you do have are already ‘old’ – even if you don’t identify as being old:) They just don’t have have the healing power they did when you were a kid. How long after a leg fracture is a child back to riding a bike? How about you? Your mother? You get my point. There is a dramatic reduction in both the number and quality of stem cells beyond the age of adolescence.

Another issue has to do with current FDA regulations that stipulate cells harvested for regenerative purposes must be re-injected same day. That’s fine if you’re injecting your own fat cells to plump your face, breasts, or back side, but if they’re being delivered systemically, they need time to be cleaned up – and less than 24 hours just isn’t enough time in my opinion. I don’t want to see anything that looks like that dripping into an IV.

Is it safe to use someone else’s stem cells? Contrary to what you might think, it most certainly is. Remember the HSCs or blood stem cells? Those are handed off from one person to another all the time. It is important to note however, that these stem cells have markers on their surfaces that can and will be recognized by the immune system. When a bone marrow transplant is performed with HSCs, the donor and recipient need to be ‘matched’ to avoid rejection.

MSCs on the other hand do not have markers on their surfaces. They are effectively ‘bald’, or ‘immuno-privileged’, we say. They go unrecognized by the immune system – stealth bomber style. You can put a healthy MSC from any donor into any recipient and there is no immune system rejection.

So bottom line, you can use your own MSCs or someone else’s 1-day old cells. I’d pick the latter, but that’s me.

 

 

 

 

 

 

References

What Happens When You Still Have Long COVID Symptoms?
https://www.yalemedicine.org/news/long-covid-symptoms

Yale Medical
www.yalemedicine.org

Selected Adverse Events Reported after COVID-19 Vaccination https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9538893/

Long COVID: major findings, mechanisms and recommendations
https://www.nature.com/articles/s41579-022-00846-2

Introduction to stem cells and regenerative medicine
https://pubmed.ncbi.nlm.nih.gov/23257690/

Human mesenchymal stem cell therapy in severe COVID-19 patients: 2-year follow-up results of a randomized, double-blind, placebo-controlled trial
https://www.thelancet.com

Stem cells: past, present, and future
https://pubmed.ncbi.nlm.nih.gov/34963099/

Human mesenchymal stem cells treatment for severe COVID-19: 1-year follow-up results of a randomized, double-blind, placebo-controlled trial
https://pubmed.ncbi.nlm.nih.gov/34963099/

Effect of human umbilical cord-derived mesenchymal stem cells on lung damage in severe COVID-19 patients: a randomized, double-blind, placebo-controlled phase 2 trial
https://pubmed.ncbi.nlm.nih.gov/33568628/

A prospective study on myocardial injury after BNT162b2 mRNA COVID-19 fourth dose vaccination in healthy persons
https://pubmed.ncbi.nlm.nih.gov/36097844/

Nearly 100,000 more deaths involving heart conditions and stroke than usual since pandemic began. https://www.bhf.org.uk/what-we-do/news-from-the-bhf/news-archive/2023/june/100000-excess-deaths-cardiovascular-disease