Umbilical cord blood is blood from a newborn baby, collected from
its placenta and umbilical cord after the cord has been clamped. Blood collected
this way at birth is utilized as a source of stem cells for transplantation, being
rich in hematopoietic stem cells.
Cord blood is stored by both public and private cord blood banks. Public cord blood
banks store cord blood for the benefit of the general public, and most U.S. banks
coordinate matching cord blood to patients through the National Marrow Donor Program
(NMDP). Private cord blood banks are for-profit organizations which store cord blood
for the exclusive use of the donor or donor's relatives.
Public cord blood banking is strongly supported by the medical community. However,
private cord blood banking is generally not recommended unless there is a family
history of specific genetic diseases. Private banking is unlawful in France and
Italy, and opposed by the European Group on Ethics in Science and New Technologies.
Cord blood harvesting is a controversial practice in the medical and parenting community.
The American Academy of Pediatrics 2007 Policy Statement on Cord Blood Banking
states that:
"Physicians should be aware of the unsubstantiated claims of private cord blood
banks made to future parents that promise to insure infants or family members against
serious illnesses in the future by use of the stem cells contained in cord blood;"
Properties
Stem cells from the blood of newborns are more proliferate and have a higher chance
of matching family members than stem cells from bone marrow. Parents and siblings
match 50% of the genetic markers of the donor's stem cell. However, since many different
genetic markers are required for a match, the probability of a potential implant
in a parent or sibling is considerably lower.
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Collection, storage and costs
Additional stem cells may be collected from the placenta via Placenta Cord Banking.
After the health care provider draws the cord blood from the umbilical cord, the
placenta is couriered to the stem cell laboratory where it is processed for additional
stem cells. By banking stem cells derived from the placenta as well as umbilical
cord blood, families may save more CD34+ stem cells for use in transplants. Having
as many of these stem cells as possible is medically important: published research
shows that the size of the stem cell transplant (especially the number of CD34+
cells) is consistently a significant factor in achieving a successful treatment
and patient survival.
There are two methods of cord blood collection from the umbilical vein: before the
placenta is delivered (in utero), and after (ex utero)
With the ex utero collection method, the cord blood is collected after the placenta
is delivered and the umbilical cord is clamped off from the newborn. The placenta
is placed in a sterile supporting structure with the umbilical cord hanging through
the support. The blood is collected by gravity drainage yielding 40-150 mL of cord
blood.
A similar collection method is performed in utero, except that the cord blood is
collected after the baby has been delivered but before the delivery of the placenta.
After collection, the cord blood units must be immediately shipped to a cord blood
bank facility. At public cord blood banks, this blood is then analyzed for infectious
agents and the tissue type is determined. Cord blood is processed and depleted of
red blood cells before being stored in liquid nitrogen for later use.
After collection, the cord blood units must be immediately shipped to a cord blood
bank facility. At public cord blood banks, this blood is then analyzed for infectious
agents and the tissue type is determined. Cord blood is processed and depleted of
red blood cells before being stored in liquid nitrogen for later use.
New parents have the option of storing their newborn's cord blood at a private cord
blood bank or donating it to a public cord blood bank. The cost of private cord
blood banking is approximately $2000 for collection and approximately $125 per year
for storage, as of 2007. Donation to a public cord blood bank is not possible everywhere,
but availability is increasing.
Several local cord blood banks across the United States are now accepting donations
from within their own states. The cord blood bank will not charge the donor for
the donation; the OB/GYN may still charge a collection fee, although many OB/GYNs
choose to donate their time.
After the first sibling-donor cord blood transplant was performed in 1988, the National
Institute of Health (NIH) awarded a grant to Dr. Pablo Rubinstein to develop the
world's first cord blood program at the New York Blood Center(NYBC), in order to
establish the inventory of non embryonal stem cell units necessary to provide unrelated,
matched grafts for patients.
In 2005, University of Toronto researcher Peter Zandstra developed a method to increase
the yield of cord blood stem cells to enable their use in treating adults as well
as children.
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Usage
When cryopreserved cord blood is needed, it is thawed, washed of the cryoprotectant,
and injected through a vein of the patient. This kind of treatment, where the stem
cells are collected from another donor, is called allogeneic treatment. When the
cells are collected from the same patient on whom they will be used, it is called
autologous treatment and when collected from identical individuals, it is referred
to as syngenic. Xenogenetic transfer of cells (between different species) is very
underdeveloped and is believed to have little research potential.
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Controversy
While there is general support in the medical community for public banking of cord
blood, the question of private banking has raised objections from many governments
and nonprofit organizations. The controversy centers on varying assessments of the
current and future likelihood of successful uses of the stored blood.
Estimates of the odds that a child will need an autologous stem cell implant by
age twenty vary widely. Proponents cite odds of around 1:2,700. The European Union
Group on Ethics has cited a paper claiming the odds are 1:20,000. The European Union
group went on to conclude that "the legitimacy of commercial cord blood banks for
autologous use should be questioned as they sell a service, which has presently,
no real use regarding therapeutic options. Thus they promise more than they can
deliver. The activities of such banks raise serious ethical criticisms."
In May 2006, The World Marrow Donor Association's Policy Statement for the Utility
of Autologous or Family Cord Blood Unit Storage stated that:
1. The use of autologous cord blood cells for the treatment of childhood leukemia
is contra-indicated because pre-leukemic cells are present at birth. Autologous
cord blood carries the same genetic defects as the donor and should not be used
to treat genetic diseases.
2. There is at present no known protocol where autologous cord blood stem cells
are used in therapy.
3. If autologous stem cell therapies should become reality in the future, these
protocols will probably rely on easily accessible stem cells.
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Diseases treated with cord blood
Beginning in the late 1980s, following a successful sibling-donor transplant, cord
blood stem cells have been used to treat a number of blood and immune-system related
genetic diseases, cancers, and disorders. Because of medical issues around using
one's own cells, in nearly every instance the treatments are done using cells from
another donor, with the vast majority being unrelated donors.
In 1993, Dr. Joanne Kurtzberg, of Duke University Medical Center, performed the
first two successful unrelated donor cord blood transplants; one of which cured
acute lymphoblastic leukemia.
The principal diseases and disorders currently treated are listed at the National
Donor Marrow Program website.
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Government initiatives to promote usage and research
United States
In 2005, U.S. Rep. Chris Smith shepherded legislation through Congress to increase
usage and research into cord blood stem cells. Smith's “Stem Cell Therapeutic and
Research Act of 2005” (P.L. 109-129), authorized $265 million for stem cell therapy,
umbilical cord blood and bone marrow treatments
The bill, which was signed into law by President George W. Bush in December of 2005,
authorizes $79 million for the collection of cord blood stem cells with the goal
of building the nation’s public umbilical cord blood supply by adding 150,000 new
units to the current inventory. The intention of the law is to collect a genetically
diverse cross-section of cord blood units in an effort to make matches available
to 90 percent of patients in need.
The law also created a national registry to match cord blood for those in need.
All the cord blood banks participating in the inventory program will be linked into
a search system that would allow transplant physicians to search for cord blood
and bone marrow matches through a single access point. In September 2006, the National
Marrow Donor Program (NMDP) was selected by the federal government to perform these
duties.
“The Stem Cell Therapeutic and Research Act of 2005” is not only aimed at increasing
the medical utilization rate for cord blood stem cells, but is also aimed at increasing
cord blood stem cell research. All cord blood collected and deemed unsuitable for
transplant is required to be donated for research.
This information is accurate as of April 2010
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List of diseases treated with cord blood from the NYBC's National Cord Blood Program
DIAGNOSIS for Transplantation with NYBC CB units Patients
Leukemias 2030
- Acute Lymphoblastic Leukemia 851
- Acute Myelogenous Leukemia 859
- Acute Biphenotypic Leukemia 29
- Chronic Lymphocytic Leukemia 27
- Chronic Myelogenous Leukemia 203
- Chronic Myelomonocytic Leukemia 1
- Juvenile Chronic Myelogenous Leukemia 34
- Juvenile Mono-myelocytic Leukemia 23
- Leukemia, Unspecified 3
Lymphomas 201
- Non-Hodgkin's Lymphoma 121
- Hodgkin's Disease 61
- Epstein-Barr Virus / Lymphoproliferative Disease 2
- Autoimmune Lymphoproliferative disease 1
- Lymphoma, unspecified 16
Myelodysplasias 186
- Myelodysplastic Syndrome 178
- Myelofibrosis 8
Bone Marrow Failure Syndromes 236
- Amegakaryocytic Thrombocytopenia 11
- Diamond-Blackfan Anemia 16
- Dyskeratosis Congenita 7
- Fanconi's Anemia 95
- Parxysmal Nocturnal Hemoglobinuria 2
- Reticular Dysgenesis 1
- Severe Aplastic Anemia, Unspecified 98
- Shwachman-Diamond Syndrome 5
- Sideroblastic Anemia 1
Hemoglobinopathies 49
- Sickle Cell Disease 20
- Thalassemia 29
Immune Deficiencies 201
- Common Variable Immune Deficiency 2
- Congenital Immune Deficiency 1
- DiGeorge syndrome 1
- Griscelli Syndrome 3
- Lymphocyte Adhesion Disease 10
- Nezelof Syndrome 1
- Omenn Syndrome 7
- Severe Combined Immune Deficiency (SCID) 113
- Wiskott-Aldrich Syndrome 55
- X-linked Hyper-IgM Syndrome 6
- X-linked Immune Dysregulation Polyendocrine Enteropathy 2
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