Cord blood is known to contain large numbers of stem cells. Currently, it is used as an alternative to bone marrow transplantation for certain conditions. Advantages of cord blood over bone marrow include the fact that it does not need to be as closely matched between donor and recipient as bone marrow does, and additionally, because the cord blood stem cells are younger, theoretically they should be more potent at re-establishing production of blood cells after a transplant.

In conventional cord blood transplants, which are usually performed for conditions such as leukemias, the immune system of the recipient is destroyed in order to allow the donor cord blood cells to engraft. Additionally, by providing large doses of chemotherapy, not only is the recipient immune system destroyed but many of the leukemic cells are also killed. The widespread use of cord blood in treatment of leukemias has led to a dogma being generated that cord blood transplants are useless when used for other treatments. Essentially, most hematologists believe that if a cord blood transplant is performed without prior treatment of the recipient with chemotherapy/immune suppressants, then one of two things will happen. The cord blood cells will either attack the recipient, a process called graft versus host disease, or conversely, the recipient immune system cells will destroy the cord blood cells, a process called host versus graft.

The current dogma, however, appears to be wrong. Firstly, cord blood administration has been performed in thousands of patients without adverse effects in absence of immune suppression. Why would someone administer cord blood for reasons besides stem cell transplants? Originally, cord blood was used as an alternative source of blood when adult blood shortages existed. The unique property of cord blood is that it contains fetal hemoglobin, which is much more effective at transporting oxygen than adult hemoglobin. Secondly, human cord blood has been used without suppression of the immune system in animal studies for conditions such as type I diabetes, ALS, and Parkinson’s Disease. The apparent ability of cord blood to induce therapeutic effects suggests that the cells were not rejected. Scientists at the Institute for Cellular Medicine have used cord blood derived cells in treatment of heart failure, which was described in a publication (Ichim et al. Placental mesenchymal and cord blood stem cell therapy for dilated cardiomyopathy. Reprod Biomed Online. 2008 Jun;16(6):898-905). The scientific rational for how cord blood stem cells may be administered without graft versus host or host versus graft reactions is provided in a paper written by the Institute for Cellular Medicine and Medistem, which is freely available at http://www.translational-medicine.com/content/5/1/8 .

A paper published today (Finney et al. Umbilical cord blood-selected CD133(+) cells exhibit vasculogenic functionality in vitro and in vivo. Cytotherapy. 2009 Nov 2.) from the Mary Laughlin’s group describes the use of cord blood cells in creation of new blood vessels. Several conditions would benefit from the creation of new blood vessels, for example, in diseases such as ischemic heart disease or peripheral artery disease, the body tries to make new blood vessels in order to compensate for occlusion in the existing blood vessels. Unfortunately, the body cannot make enough new blood vessels to keep up with demand. If cord blood stem cells could be used to make new blood vessels, this treatment would have numerous applications.

In the publication, the researchers describe that cord blood contains a higher number of cells expressing the CD133 marker. These are cells that on the one hand can make new blood cells (called hematopoietic stem cells), but have also been postulated by others to have the ability to generate the cells that line the blood vessels (endothelial cells).

By culturing purified cord blood CD133 cells with existing blood vessel cells outside of the body, the scientists found that the CD133 cells would increase the rate at which the blood vessel cells multiplied. Using this knowledge, the next question was whether the CD133 cells could stimulate formation of new blood vessels in animal models.

One of the major arteries that feeds the leg, called the femoral artery, was blocked in order to mimic conditions of decreased blood flow. Usually this results decreased function of the leg and death of muscle tissue. Administration of CD133 cells was shown to stimulate new blood vessel formation, preserve leg function, and decrease the amount of cell death in the digits of the mouse limbs. Activity of CD133 cells derived from cord blood seemed to be higher than that of bone marrow derived cells.

These studies suggest that cord blood derived stem cells may be therapeutically useful in conditions requiring formation of new blood vessels. In fact, a company called Medistem actually has filed patents on the use of drugs already approved for other indications in order to modify umbilical cord blood to increase potency in the stimulation of new blood vessels in patients with critical limb ischemia, an advanced form of peripheral artery disease.

Stem cells that make blood are heavily concentrated in the bone marrow. These cells are called "hematopoietic stem cells". When patients with leukemia are given a bone marrow transplant, they first receive high doses of radiation and chemotherapy in order to kill both the leukemic cells, as well as the healthy blood cells in the bone marrow. Subsequently the patients are given healthy bone marrow from a patient that has been matched immunologically. The new bone marrow contains high numbers of stem cells that take over the task of making new blood cells for the body. In some situations the leukemia comes back, however a bigger cause of mortality is when the blood cells made by the new bone marrow start attacking the recipient. This is a condition called graft versus host.

One of the advancements in bone marrow transplantation was the use of stem cells collected from the blood instead of the bone marrow. While under normal circumstances there are very little hematopoietic stem cells circulating in the blood, it was observed many years ago that after administration of certain compounds, the number of stem cells in the blood increases. This led scientists to try to find agents that can be used in patients that make stem cells leave bone marrow and enter circulation. There are three reasons why this would be important. Firstly, the process of extracting bone marrow from donors is very difficult. It involves sometimes more than 30 punctures into the hip bone. Secondly, there is some evidence that when the stem cells are collected from the blood, they have less potential to stimulate graft versus host disease. Thirdly, outside of the context of transplantation, it is known that bone marrow stem cells have ability to accelerate healing of tissues. Thus if there was a drug that could induce stem cells to leave the bone marrow and enter circulation, this drug would have many benefits.

The first stem cell mobilizer to be approved was granulocyte colony stimulating factor (G-CSF). This is a protein that is made by many cells in the body, especially by cells of the immune system. G-CSF specifically tells the bone marrow cell to make more granulocytes, these are cells that fight infections. In the process of infection, cells of the immune system called macrophages, start to produce G-CSF in response to bacteria and cause production of granulocytes which can then go and fight the bacteria. Interestingly, it was found that G-CSF also would instruct the bone marrow stem cells to exit the bone marrow and enter circulation.

This led to a variety of studies demonstrating that G-CSF "mobilized" stem cells can be collected from the blood of donors and used as an alternative to harvesting of donor bone marrow. In the majority of hospitals that perform transplants, donor collection is now performed by mobilization of stem cells.

Studies have reported that stem cells mobilized by G-CSF appear to have some beneficial effects in patients who have had heart attacks. Other studies have shown that stem cells mobilized by G-CSF may help patients with heart failure due to poor blood supply to the heart. For example, Maier et al. published a paper (Myocardial salvage through coronary collateral growth by granulocyte colony-stimulating factor in chronic coronary artery disease: a controlled randomized trial. Circulation. 2009 Oct 6;120(14):1355-63) in which 52 patients suffering from coronary artery disease were given either placebo or G-CSF for 2 weeks. Increases in the blood supply to the heart, and heart function were observed in the treated patients.

Currently G-CSF sells more than a billion dollars a year for use in a variety of diseases. Since the original patents on G-CSF have expired, there has been a great interest in the development of other stem cell mobilizers. However, to develop newer drugs that cause mobilization, it may be worthwhile to discuss the mechanisms by which G-CSF induces this process. It is known that in transplantation of stem cells, that the recipient can receive stem cells intravenously, but somehow they home to the bone marrow. This homing mechanism is mediated by the protein stromal derived factor (SDF)-1, which is made at a stable rate by the other cells in the bone marrow that are not stem cells. The hematopoietic stem cells recognize concentrations of SDF-1 based on receptors called CXCR-4. When G-CSF is administered, numerous biochemical pathways are activated that seem to converge, at least in part, to disrupting the interaction between the SDF-1 made by the bone marrow and the CXCR-4 that is on the stem cells.

The company Anormed recognized the importance of this interaction and started making chemical drugs that would block it. As we stated, G-CSF causes a variety of biological effects, however, by selectively targeting the essential interaction, the ability to increase mobilization should theoretically be more potent. Indeed, Anormed developed the drug Mozobil, which appears to be 10-100 times more potent than G-CSF at mobilizing stem cells, and was sold to Genzyme in a deal worth half a billion dollars. Mozobil received FDA approval and is currently used alone or sometimes in combination with G-CSF.
Recognition of the importance of the SDF-1-CXCR4 interaction led the company NOXXON to develop drugs to target this. However, unlike Anormed, which used conventional small molecules, NOXXON used a new technology called Aptamers, which are nucleic acids that can be engineered to specifically block interactions between proteins. The process of generating aptamers to target proteins involves selection in vitro, which can be accomplished at a more rapid rate as compared to what can be done for small molecules.

Today NOXXON announced that is has successfully administered its NOX-A12 aptamer-based mobilizer to healthy volunteers as part of a Phase I clinical trial. Usually the purpose of a Phase I trial is to determine the distribution of a drug in the human body, and to test for possible adverse effects. The dose chosen from a Phase I is then used to conduct Phase II studies in which biological effect is tested. The NOX-A12 trial was conducted in Germany with the approval of the Clinical Trial Application by the Federal Institute for Drugs and Medical Devices (Bundesinstitut für Arzneimittel und Medizinprodukte, BfArM). The study is evaluating effects in 42 volunteers with the aim of assessing efficacy in patients with multiple myeloma or non-Hodgkin’s lymphoma in a Phase II trial that is planned for mid 2010. The company states that it plans to obtain marketing approval by 2014. Marketing approval for a drug is granted after 2 double blind, placebo controlled, Phase III studies are performed in which the primary endpoints show a statistically significant improvement over placebo.

The choice of multiple myeloma or non-Hodgkin’s lymphoma as conditions for evaluating NOXA-A12 may be due to the high incidence of patients with these conditions who are poor mobilizers. In these conditions, part of the protocols used clinically, involve mobilizing the bone marrow, administration of chemotherapy, and subsequent reintroduction of the bone marrow into the body.

The adult stem cell company Aldagen Inc, from Durham North Carolina announced today that it has filed a registration with the Securities Exchange Commission for an initial public offering with a potential value of $80.5 million. Details regarding price range or shares to be issues were not disclosed.

Aldagen is one of the adult stem cell companies in advanced clinical trials in the United States. The technology that they are developing is based on intellectual property covering the use of a specific enzyme, aldehyde dehydrogenase (ALDH), as a means of selecting stem cells with higher level of potency from adult sources. Although the particular type of stem cells that Aldagen is selecting for are stem cells that make blood, called hematopoietic stem cells, the company’s technology has been shown to select for other stem cells as well.

It’s most advanced program, is ALD-101, a purified cord blood stem cell product for treatment of inherited metabolic diseases in pediatric patients. This is in Phase III clinical trials, which means that the safety (Phase I) has been demonstrated, that preliminary efficacy (Phase II) has been demonstrated, and now what remains to be demonstrated is efficacy of the product in a double blind, placebo controlled study (Phase III). Several metabolic diseases have been successfully treated with stem cells from the cord blood. Conditions such as Krabbe Disease, involve defective biochemical pathways in cells that original from stem cells. By administration of new stem cells that express the correct biochemical and genetic components, the functioning cells end up taking over the function of the nonfunctioning cells.

The company is also preparing to conduct a Phase III clinical trial for critical limb using its product ALD-301. This product involves extraction of patient bone marrow, purification of cells expressing ALDH, and re-administration of the purified cells into the muscles of patients with critical limb ischemia. The rationale for this treatment is that patients with critical limb ischemia lack appropriate circulation in their legs and are at risk of amputation. By administration of the patient’s own stem cells, the cells are believed to stimulate the production of new blood vessels, which theoretically will reduce the need for amputation. Previous studies using stem cells for treatment of critical limb ischemia have demonstrated successful results in terms of improved walking distance and increased circulation (Kawamoto et al. Intramuscular Transplantation of Granulocyte Colony Stimulating Factor-Mobilized CD34-Positive Cells in Patients with Critical Limb Ischemia: A Phase I/IIa, Multi-Center, Single-Blind and Dose-Escalation Clinical Trial. Stem Cells. 2009 Aug 26), to our knowledge, the proposed Phase III trial will be the first FDA registration trial for use of stem cells in critical limb ischemia.

Additionally, Aldagen is developing ALD-201, which uses the patient’s own bone marrow derived stem cells, but instead of administering them into the ischemic leg, they are administered into the heart muscle by means of a specialized catheter. Currently ALD-201 completed a Phase I trial. In contrast to other cardiac clinical trials involving administration of stem cells after a heart attack, this is one of the few trials that is treating patients with chronic heart failure. Essentially the concept is that the stem cells will be able to create new blood vessels, which will help by providing more oxygen to the cardiac muscle, as well as stimulate stem cells that are resident in the heart through the production of various growth factors.

The company is performing several areas of investigation, including purification of cancer stem cells using their technique, as well as expansion into other disease conditions such as stroke and improvement of post-transplant reconstitution.

As with many biotechnology companies, Aldagen is not expected to be profitable in the close future. In the first nine months of 2009 the company spent 9.7 million, while a year ago it spent $13.8 million. The majority shareholder is Intersouth Partners, an early-stage venture capital who invests in companies in the South East US. Intersouth owns 41.6 percent of Aldagen. The underwriters of the IPO are Cowen and Co. and Wells Fargo Securities. A copy of the full S-1 filing may be obtained at the SEC website http://www.sec.gov/Archives/edgar/data/1128188/000119312509215575/ds1.htm

Once again, adult stem cells derived from adipose (fat) tissue are in the news for the therapeutic promise that they offer in the treatment of a number of diseases, especially heart disease.

Dr. Stuart Williams of the University of Louisville and the Cardiovascular Innovation Institute in Kentucky is currently in the process of designing a clinical trial, which he anticipates will commence within 9 months, in which adipose-derived adult stem cells will be tested in the treatment of patients with heart failure. He then realistically believes that an adipose-based adult stem cell therapy will be widely available in the U.S. within 3 to 5 years.

A number of studies have already been completed in which adipose-derived adult stem cells have been tested as a therapy for heart failure, with extremely positive results. Current similar studies are also in the process of being repeated on cardiac patients in Spain.

According to Dr. Keith March, director of the Vascular and Cardiac Center for Adult Stem Cell Therapy at Indiana University, "These sorts of cells are extremely readily available and abundant, and their normal function is tissue repair." As Dr. Williams half-jokinglly adds, "God made love handles for a reason."

Dr. Williams, a recognized pioneer in the field of adipose-derived adult stem cells, was originally inspired to investigate fat cells years ago when he met Dr. Martin Rodbell, a biochemist at NIH (the National Institutes of Health) who had won the Nobel Prize in Physiology or Medicine in 1994. Dr. Rodbell’s research interest at that time had focused on adipose cells from rats, especially those cells that floated to the tops of the test tubes. Dr. Williams, on the other hand, became curious about the denser fat cells that sunk to the bottom, and began to investigate their properties. Willliams was later awarded a U.S. patent for developing a method by which stem cells are isolated from adipose tissue – the same method that is employed today by research specialists in laboratories around the world.

The International Federation for Adipose Therapeutics and Science (IFATS) has estimated that there are approximately 300 scientists in the U.S. today who are studying adipose-derived stem cells, with approximately 10 laboratories that are exclusively focused on the topic.

Although adipose-derived adult stem cells have proven to be highly potent, capable of differentiating into a wide variety of tissue types, a few safety questions still remain unanswered. According to Dr. Yong-Jian Geng, for example, director of cardiac research at the Texas Heart Institute, "The main concern is we don’t want to develop fat tissue in the heart."

Whatever discoveries might ultimately be made regarding the clinical viability of adipose-derived stem cells, the ongoing research and clinical trials are an important part of that discovery process. As Dr. Williams further explains, "It’s like space travel. You do it because it’s there. You do it because it’s science and it’s the unknown."