Organ Transplants: Making Old Organs New Again - NewsChannel5.com | Nashville News, Weather & Sports

Organ Transplants: Making Old Organs New Again

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LOS ANGELES, Calif. (Ivanhoe Newswire) - It's a list no one wants to be on.  More than 90,000 people are waiting for an organ transplant right now, but one doctor hopes to get that list down to zero.

The numbers can be overwhelming, but what's inside this petri dish could change everything.

"It has never been done before," Roger De Filippo, MD, Director of the Saban Research Institute, told Ivanhoe.

Stored inside this lab at the children's Hospital in Los Angeles, Dr. Roger De Filippo is using stem cells taken from amniotic fluid, which surrounds fetuses in the womb, to heal damaged kidneys.

"What we found was the cells were able to regenerate the normal tissue in the kidney and become part of the kidney," Dr. De Filippo said.

The stem cells can actually help a dying kidney fix itself.

"In this flask here you have a number of regenerated kidneys," Dr. De Filippo explained.

The doctor believes the same stem cells could be injected directly into a patient's diseased organ.

"Become part of that organ, even regenerate the necessary building blocks of that organ," Dr. De Filippo said.

It could change the future for people suffering from acute kidney disease, diabetes and genetic disorders.

"Slow down the progression of the disease pretty significantly," Dr. De Filippo stated.

Don't confuse embryonic with amniotic. The stem cells used to regenerate kidneys are from fluids collected after childbirth.  There is an endless supply of them.  This type of cell can not only be used for kidneys, but they can adapt to any other type of organ as well.

RESEARCH SUMMARY

BACKGROUND:   An organ transplant replaces the failing organ with a healthy organ. Organs most often transplanted include:

  • The kidney, resulting from diabetes, lupus, polycystic kidney disease, or other problems
  • The liver, resulting from cirrhosis
  • The pancreas, resulting from diabetes
  • The heart, resulting from cardiomyopathy, coronary artery disease, heart failure, and other heart complications.
  • The lung, resulting from COPD, cystic fibrosis, and other problems.
  • The small intestine, resulting from short bowel syndrome caused by necrotizing enterocolitis, Crohn's disease, and other problems.  

Not everyone is a good candidate for an organ transplant.  Infection, drug or alcohol abuse, heart disease that is out of control and other serious health problems will disqualify someone from receiving an organ transplant.  The United States has been doing organ transplants since the 1950s.  The procedure has not stopped improving since then. (Source: www.webmd.com)

HOW TO PREPARE:  The first step in an organ transplant procedure is finding a match by conducting blood and tissue tests.  This is done because the immune system may detect the new organ as foreign and reject it.  The more matches with the donor, the greater the chances of the body accepting the donor organ.  Patients who qualify for a transplant are advised to continue their medications, get regular blood tests, and to talk to a psychologist or psychiatrist about the transplant. (Source: www.webmd.com)

NEW TECHNOLOGY:  Stem cells have been all over the news in the past and there is speculation over using stem cells to help with a serious disease. Stem cells are the body's raw materials (cells from which all other cells with specialized functions are generated from).  Stem cells can divide to form daughter cells.  The daughter cells can then become new stem cells or specialized cells with a more specific function, like brain cells, heart muscle, blood cells, or bone.  Stem cells can come from amniotic fluid, adult cells altered to have properties of embryonic stem cells, adult stem cells, and embryonic stem cells.

In 2007, scientists discovered that stem cells can be found in amniotic fluid that's discarded after birth.  Now researchers are able to take the stem cells from amniotic fluid to help fix a dying organ.  This could provide an alternative to organ transplantation.  Researchers hope that the amniotic cells can be frozen and banked in the same way blood is, and patients in need of blood vessel repair would be able to receive the cells through an injection.  Also, they hope that the cells could be injected right into the dying organ to help repair it.  They hope the cells could regenerate the tissues in the kidney and become part of the kidney. (Source: www.weill.cornell.edu) 

INTERVIEW

Dr. Roger De Filippo, principal investigator at The Saban Research Institute of Children's Hospital Los Angeles, talks about building organs in the laboratory.

So you see firsthand how a kidney and the failure of kidneys can affect someone from birth?

Dr. De Filippo: Yes. We deal with a lot of congenital conditions. Kids that are born with conditions that would mean significant compromise to their kidney function. We operate on a lot of children that have conditions of the kidney that require extensive reconstruction. It is a part of what we do every day.

A lot of kids come through your hospital that would really benefit from kidney transplants and have to stay on the list for a long time. Do you see their health fail? 

Dr. De Filippo: There are a lot of patients today waiting on a transplant list for kidney transplant. While they are waiting, they require dialysis. Having research that could potentially offer them other alternatives is worth pursuing.

And part of that is regenerative medicine right?

Dr. De Filippo: Certainly; regenerative medicine, bioengineering, tissue engineering, all of that is an important aspect of the work that we are doing in the laboratory.

Can you tell me a little bit about that the kidney that you are building in the lab?

Dr. De Filippo: When we first started here, nearly 10 years ago, one of our focuses was regenerating kidneys in the laboratory. So we were actually able to do that with kidneys on a small scale, using stem cells that we were able to retrieve from amniotic fluid. Amniotic fluid is a very good source of stem cells and other cells that lend themselves to regenerative medicine, tissue engineering, and bioengineering. That was actually one of our first projects in looking at our ability to use concepts in embryology and developmental biology to reconstruct these kidneys. We were actually able to insert these cells into small developing kidneys and what we found was that these cells were able to regenerate tissue and would become part of the kidney.

Was that a surprise? 

Dr. De Filippo: Well it had never been done before. We were hypothetically thinking that that would happen, but it certainly was a pleasant surprise to see it occur.

Is it just regenerating cells in your own kidney?

Dr. De Filippo: We have 2 basic lines of research in our laboratory; one very classic tissue engineering line where we are building kidneys with scaffolds using regenerative cells. These are the cells that were destined to become various parts of the kidney that we were able to isolate from amniotic fluid. We are also using a cell therapy, where we are able to inject these cells into damaged kidneys or kidneys that would eventually succumb to their disease and fail, and we are able to stave off organ failure.

Does it stop the disease in its progression? What types of diseases are you talking about? 

Dr. De Filippo: We have a model right now for chronic kidney disease, which we are working on. We are replicating conditions that in a human would require dialysis. What we are finding is using this cell therapy; we are actually able to slow down the progression of the disease pretty significantly. 

How much?

Dr. De Filippo: We have some models right now that have received recurrent therapies and that we have been able to basically preserve their renal function to where they are not having any signs or any significant signs, of end stage disease in other words.

Does that suggest that in the future, using these therapies, someone could be able to get off of dialysis?

Dr. De Filippo: That is certainly our hope to delay the need for dialysis quite significantly. That alone would be a very significant improvement over what we have now. The longer you can delay dialysis, the better it is for the patient. An analogy could be someone taking insulin for diabetes. If we could give our patients a therapy that would be similar to that, so that they would not succumb to their disease so early; that certainly would allow them to live a normal life with their disease.

Do you see these future therapies cutting down on the need for transplant?

Dr. De Filippo: Our hope would be that we would have fewer patients on a transplant list. That would mitigate the pressure that is on that list right now because you have a lot of patients and very few organs available.

Why use amniotic stem cells instead of the more well known, but controversial, embryonic stem cells? 

Dr. De Filippo: Well, we have been working with this source of cells for quite some time, over 10 years. There are a lot of advantages with amniotic fluid stem cells; they are cells that are easily retrievable. They present very little in the way of harm for either the baby or the mother. They are cells that you can acquire in very large number, so for regenerative medicine purposes, or for tissue engineering purposes, that is very appealing because you need a lot of cells to basically build organs in the laboratory and you need a lot of cells for cell therapy. Amnionic stem cells don't form tumors like your classic embryonic stem cells. They also don't come with a lot of the ethical concerns associated with perhaps other embryonic stem cells lines. Yet, they are what we call pleury-potent so they can be differentiated into a variety of cell types and, therefore, be used for a variety of purposes. For these reasons, they are very appealing to bioengineers, tissue engineers, and regenerative medicine scientists.

Do you think it is too early for parents to start thinking about embryonic stem cell banks?

Dr. De Filippo: Not at all. This is a very exciting time for stem cell biologists and scientists everywhere. It is also interesting to think in terms of parents banking stem cells. Currently, parents are banking of cord blood and, so far, that is just a single stem cell type. As clinicians, we are faced with the fact that one cell type is not going to be ideal for everything we may need a variety of cell types to have at our disposable to treat diseases in a child's future.

Can you list off 4 or 5 different kidney diseases that you are specifically working on?

Dr. De Filippo:  We are working on acute kidney disease like acute tubular necrosis. We have a model for diabetic nephropathy, kidney disease related to diabetes. We are working on an Alport model in the laboratory that is a genetic disease that is a form of chronic kidney disease and ultimately can lead to kidney failure. Those are the 3 main models that we are working on right now. 

How long until you begin treating patients in clinical trials?

Dr. De Filippo: We are very hopeful that some of our cell therapy work could be realized within the next 5 years. I think that is certainly a very realistic goal of ours. The cell therapy work that we are doing for chronic kidney disease could be in patients in the next 5 years. I think we have some very good data to support this projection and we are doing our best to make it happen.

Do you think the controversy surrounding stem cells is holding scientists back here in America compared to other countries?

Dr. De Filippo: What makes it great to work in a country like ours is that we can have those discussions and address the, issues.  It allows us, as scientists, the opportunity to educate our colleagues and educate the population. I don't think those are actually apprehending our discussions create obstacles in the long run. That being said, there are also alternative sources of stem cells, such as the amniotic fluid stem cells we are using in our lab, that tend to avoid many of the ethical issues.

FOR MORE INFORMATION, PLEASE CONTACT:

Ellin Kavanagh
Senior Public Information Officer, Research
Marketing Communications Department
Children's Hospital, Los Angeles
(323) 361-8505
ekavanagh@chla.usc.edu

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