Stem cells shown safe, beneficial for chronic stroke patients
med.stanford.edu
med.stanford.edu
MSC's can be harvested from one's own adipose tissue with a little bit of liposuction.
The process of separating the stem cells from fat is called stromal vascular fraction.
It's an astoundingly easy process to do [1]. The equipment is inexpensive, and so far the procedure has been shown to be safe.
MSC's have been shown to improve COPD, and reduce the allergic response that triggers asthma. Skin damage healed, cartilage and joint injuries repaired, and even MS put in to remission,
MSC's administered via IV flock to areas of inflammation and damage and begin to repair it. The cells know what to do. Local administration is even better, as in this study or in cases of back pain and joint injuries.
Autologous treatments should not be considered biological drugs and subject to monopolization by biotech companies through decade long clinical trials and FDA approval.
These are our own cells from our own bodies. Doctors should be free to practice and innovate in this sphere, and in this case innovation is mostly just dosage, frequency and delivery method because the cells know what to do.
I believe that in the next decade or two, autologous stem cell treatments will be basic preventative care for everyone, a treatment each year will repair damage before it becomes pathology.
[1] https://www.miltenyibiotec.com/~/media/Files/Navigation/Rese...
What we and others have found is that age of the donor inversely correlates to their therapeutic potential. For that reason, I founded Forever Labs, Inc. http://www.foreverlabs.co/
We bank young MSCs so that they can be preserved for therapy later in life. I banked my own two months ago.
We prefer bone marrow MSCs as the BM also contains blood progenitor and stem cells, whereas adipose tissue does not.
*We are fast expanding and raising; email in bio. ;)
Is it a store that depletes as you use it? Or can banked stem cells be replicated to create more reserves?
We don't expand the cells at this time, but will likely offer expansion services in the future.
Yes, by expanding you could create a very large reserve of cells.
I'm glad to hear about your company. And I'd kind of proud that my intuition proved correct, even though I don't know much about the field.
At what (maximum) age would the max potential benefit be achieved from harvesting? (ie, I assume it doesn't make sense for an infant to have this procedure, but assuming it's available throughout one's life, when would be the optimal time to do it?)
Yes.
>At what (maximum) age would the max potential benefit be achieved from harvesting?
Functional data of cells harvested from donors of different ages shows much variability between individuals, but after about 40, a slow trend in decreased differentiation potential, proliferation, and other measures, appears. The decline depends upon the measure, but in general, suggests 20-40yo is the best window, and closer to 20 is likely better. The functional decline continues, but seems to get steeper around 60. Between 70-80, some studies report that the numbers of stem cells start to drop in addition to function. Here is a representative study: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2398731/
MSC benefits are fantastic at replacing lost or damaged cells, however they are not bio-rejuvenation in the sense of turning back the clock with younger cells, unless one were to bank one's own younger cells?
If that is true, it would be, in a sense, an early SENS hack.
Very interesting. Will contact.
There has been some animal work that suggests transplantation may have that effect:
http://www.ncbi.nlm.nih.gov/pubmed/23967009 http://www.ncbi.nlm.nih.gov/pubmed/25707248
There is much research to be done, but the technology to transplant young bone marrow stem cells to one's older self exists today.
To be honest, that is part of my personal motivation. 'Autologous stem cell time travel' is low hanging fruit. We preserve the cells in multiple aliquots with the assumption that they might be used for multiple purposes, including expansion.
- you're using bone marrow stem cells and using the same confusing acronym as mesenchymal stem cells. As someone who has been out of active research for several years, what is the difference? And are there other acronyms that are accepted?
- BM stem cells through bone marrow harvest used to be the order of the day for repopulating immune systems following irradiation of marrow for some leukemias. Nowadays the state of the art is that those stem cells can be harvested by fractioning whole blood, so you only have the hassle of a blood donation, rather than the serious and not to be sneezed at act of penetrating cortex to harvest marrow. Is there any reason you can't get this from whole blood?
Thanks
>Is there any reason you can't get this from whole blood?
The blood harvest process uses a machine, takes a few hours, and requires the prior administration of a protein that stimulates stem cell proliferation and release into the blood. It is preferable for some procedures, but for those reasons, not for ours.
It's not bad at all.
If you are interested, contact us, and let us know where you are at.
The procedure is done with a local anesthetic. The entire procedure takes about 15 minutes from lying down to standing up. It is drawn from the upper part of your pelvis bone on your lower back. The most discomfort is a muscle cramp-like feeling that lasts about 5 seconds upon the draw itself. Personally, I rated it a 3.5 out of 10, as did my wife. Consensus is 3-4. Our CEO is a self-professed wimp, and he said it was a 4. :) I'd much prefer it to a cavity being filled. There is no recovery, just a bruise-like tenderness at that exact spot for a few days. I walked across town for lunch afterwards.
http://www.foreverlabs.co/uploads/4/9/3/9/4939113/5557005_or...
Induced stem cells (IPS), or stem cells that are genetically modified may carry these risks, as there is overlap in the signaling mechanisms that maintain the undifferentiated state of stem cells, and that of tumor. In fact, stem cells naturally express more tumor-suppressing proteins as they age, which is thought to be a mechanism to prevent tumorigenesis resulting from damage accrued in the cells over time.
After I sign up for an information session, it says last name is mandatory even though I clearly filled it out.
FYI.
According to this article, what you're referring to is just the FDA putting stem cells under the same regulatory burden as most drugs.
https://www.statnews.com/2016/02/08/fda-crackdown-stem-cell-...
They have escaped this previously because the stem cells came from the patient, and not much was done to the cells before re-injection, so it's closer to plastic surgery.
I happen to think that that FDA is probably way too conservative (both on stem cells and drugs) and seriously inhibits progress, but I think it's misleading to suggest that they are slowing progress in a way specific to stem cells. The FDA has always had a mission to not just protect patients from harm, but also from being fleeced by useless sham therapies.
That the FDA has overturned its own history and precedent is the scandal, imho.
A benefit has been shown, to what degree and in which circumstances is being ironed out.
There is some hope, the FDA has liberalized to some degree in recent years and biotech has been a top performing sector. We live in miraculous times.
That said they were not autologous mesenchymal stem cells. This study gives hope.
Refs: http://www.nature.com/stemcells/2009/0902/090226/full/stemce...
http://journals.plos.org/plosmedicine/article?id=10.1371/jou...
Old review from early 2000s http://onlinelibrary.wiley.com/doi/10.1002/ana.60000/full
> In this case the therapy is not useless or a sham
More precisely, in this case you believe there is enough evidence that the therapy is effective, but the FDA does not yet agree that has been established. Then, in congruence with its policy on unproven medical procedures, the FDA has severely constrained stem cell procedures.
> and it is autologous which has traditionally been an exempt area in this respect.
It's clear that there was little/no enforcement in this area previously, but now they have announced clarification that it is to be enforced. You may call that a change in the regulatory environment, but it doesn't appear to be a change in general policy.
The situation is very similar to 23andMe. 23andMe was flying under the radar and, when the FDA cracked down on them, they experienced a changed in their effective regulatory environment, but this is not reasonably interpreted as the FDA changing its tune (or overturning history or precedent or whatever).
Again, I wish the FDA allowed more of these things to proceed (including 23andMe and stem cells) but I don't think this is change.
But I can imagine that attempted smears-by-association (as you you are positing above) are common currency, in those communities.
The "within reason" part is very important: As in, someone on their deathbed might have to go through certain hoops to get not-yet-approved treatment X (like signing waivers saying they understand the risks, etc); and there might other minimalist safeguards in place (such as that the chemicals are manufactured at regulated facilities; that the persons involved in administering the treatment have no criminal records or major fraud convictions against them) -- but ultimately, they can get access to treatment X.
By tweaking this to an extreme absolutist position -- "there should be no regulation of end-of-life treatments, of any kind, whatsoever; even if the person offering the trade is a convicted criminal and/ con-artist" you are standing up a false argument that the original commenter wasn't making.
Edit: not intended to sound ad hominem
b) The phrase you're looking for is "argument from authority," which it is.
b) Sometimes people cry 'ad hominem' after any statement that refers to the debating party ('you') and I wanted to avoid that.
I worked at a medical startup that was bought by JNJ, it was high end surgery technolgy.
We made the first gen of our product, and it took 14 months to clear fda. Even though we made lots of improvments to the devices after, we never released them; that would have caused another horible fda clearance process.
> Caplan suggested that giving Josh the drug through the compassionate-use protocol might endanger its approval by the FDA. In the worst case, Josh would die after taking brincidofovir, and that outcome would “be held against the drug and the company until they can show the drug did not kill him.” In the meantime, other patients would find their access to the drug severely restricted. What’s more, an online campaign powered by photographs of a sick little boy raised hard questions about fairness. “Those who are not very cute get less attention in their pursuit of unproven drugs,” Caplan wrote. “If Josh had parents who did not understand how to use social media, he would already be out of luck.”
My grandfather died of COPD, and likely so will my Dad. He has COPD. And was diagnosed in his 50s. I am fearful of it myself, but thankfully unlike both of them I've never smoked.
It is a shot in the dark, but do you know anything off hand of having him participate in something like this in the US?
It seems like the doctors that have been performing are silos of information right now. There is not a lot published on the web of their experience as practicing doctors, some of the best on the ground info I have found is from interviews of doctors practicing.
There are also very many published MSC trials showing a benefit.
It is a terrible thing to not be able to breathe well. I hope that this can help.
I don't want to travel to Mexico or Thailand or even Europe to have this simple procedure, and I don't want to wait 10 or 15 years and then have to pay monopolist, proprietary pricing for what would be an inferior technique compared to what a free, open source medical science would inevitably produce.
http://www.san-bio.com/product/
The brain is immune privileged, so there is more leeway to use donor cells if that is the destination. Which isn't the case in most uses of stem cell transplants, as you point out.
https://www.nih.gov/news-events/nih-research-matters/lymphat...
So I'm inclined to think that this is one of a number of different studies in recent years to demonstrate that the delivery methodology makes just as much of a difference as the type of cell lineage and any tinkering done to that cell lineage.
[1] https://www.reddit.com/r/IAmA/comments/fu2ub/as_requested_i_...
https://www.whitehouse.gov/the-press-office/removing-barrier...
What got swept under the rug was that at the same time, President Obama specifically rescinded a previous executive order that directed the HHS to "conduct and support" research using adult stem cells:
https://www.cellmedicine.com/obama-executive-order/
I don't think the Obama administration ever spelled out why, at the same time it was promoting ESCR, it decided to also deprioritize adult stem cell research, but I think this latest news -- along with all of the other advances of the past eight years -- has shown that moral issues aside, adult stem cell research is paying high dividends.
It was all part of the same EO, which was accompanied on the same day by a Presidential Memorandum on scientific integrity in government decisionmaking on science and technology, and the rationale for the set of policy changes was explicitly to move toward allowing decisions on what avenues of science to pursue (not the goals, but the routes to the goals) to be guided by science rather than politics.
It wasn't deprioritizing adult stem cell research, it was letting the relative priority of adult stem research be set, and adjusted, over time based on science, rather than being set by political directive.
The next step is intervention versus placebo. Strokes are very common. It should be easy to find patients to enroll.
Hopefully this will turn out to work and be worth the cost.
With one intervention using donor cells in 12 months, for stroke patients, that could be a big deal.. with improvement to the procedure or combining with other treatments maybe more could be achieved.
Also the improvements continues after the stem cells have disappeared. This seems to suggest the effect doesn't come from the MSC, but rather the chemicals the cell produces. Does that mean if we can synthesis the chemicals, we don't need the cell?
Users here are simply expected to live by the spirit of the law—civility and substantiveness—when commenting here. Snarky one-liners that characterize a (vague) opposing view as "killing human beings" fail the "civil and substantive" test. Plus there's outright rudeness in comments such as https://news.ycombinator.com/item?id=11663455 and https://news.ycombinator.com/item?id=11651181, which has no place here.
The other two (chronologically disordered) examples are a product of my indignation with an obstinate person who wasted people's time and, brazenly ignoring their arguments as well as my own, continued arguing FUD.
Bottom point: I am not malicious and I contribute. So I'd appreciate if the trigger was not pulled on me even though it's probably the only way to get one's comments removed from here :-/
If you want to argue semantics of the words or the phrase, we can do that. If you want me to use a dictionary to justify my use of the words "human" and/or "being", I'll do that. If you want textbook (medical) definitions, you can have it right away at https://goo.gl/ZFDcbg. And if you'd like more scientific literature backing, consult https://goo.gl/zXpbAu. If you are willing to cede that the nomenclature fits, but would like to now rank human beings by worth in relation to stage of development, I would like to provide arguments for why you shouldn't do that. Finally, if you have reconsidered everything, I would invite you to the Way, the Truth and the Life, as scary as that might sound. Peace be with you and yours.