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Stem Cell and Neonatology
Dr. Vinayak V. Kodur
1st year DM resident
L.T.M.General Hospital.
Stem Cell History
1998 - Researchers first extract stem cells from human
embryos
1999 - First Successful human transplant of insulin-making
cells from cadavers
2001 - US President George Bush restricts federal funding
for embryonic stem-cell research
2002 - Juvenile Diabetes Research Foundation International
creates $20 million fund-raising effort to support
stem-cell research
2002 - California ok stem cell research
2004 - Harvard researchers grow stem cells from embryos
using private funding
Stem Cell Definition
• A cell that has the ability to continuously
divide and differentiate (develop) into
various other kind(s) of cells/tissues
Kinds of Stem Cells
Stem cell
type Description Examples
Totipotent
Each cell can develop
into a new individual
Cells from early
(1-3 days)
embryos
Pluripotent
Cells can form any
(over 200) cell types
Some cells of
blastocyst (5 to
14 days)
Multipotent
Cells differentiated,
but can form a
number of other
tissues
Fetal tissue, cord
blood, and adult
stem cells
Kinds of Stem Cells
• Embryonic stem cells come from a five to six-day-old embryo.
They have the ability to form virtually any type of cell found in the
human body.
• Embryonic germ cells are derived from the part of a human
embryo or foetus that will ultimately produce eggs or sperm
(gametes).
• Adult stem cells are undifferentiated cells found among specialized
or differentiated cells in a tissue or organ after birth. Based on
current research they appear to have a more restricted ability to
produce different cell types and to self-renew.
Comparison of Stem
Cell Sources
Umbilical
Cord
Adult Embryonic
1
Ability to differentiate into
various cell types
✓ ✓ ✓
2
High proliferation
capacity
✓ ✓
3
Low risk of tumor
formation
✓ ✓
4
Low risk of viral
contamination
✓ ✓
5
Capacity for autologous
transplantation
✓ ✓
6
Established/proven
treatment in human
patients
✓ ✓
Cord Blood Stem Cells
• Advantage: biologically, a greater degree of human
leukocyte antigen mismatch is tolerated by the recipient
and the incidence of acute graft-versus-host reaction is
decreased when umbilical cord blood is used.
• The predominant disadvantage of umbilical cord blood
use is related to the low number of stem cells acquired
per unit. However, the use of combined units of umbilical
cord blood allows for the expansion of umbilical cord
blood volume (and increased number of stem cells) to
be used for adult hematopoietic transplants.
• Studies are currently underway evaluating the feasibility
of ex vivo expansion of the units
Blastocyst formation
Adult Stem Cell
Few diseases treated with stem cells
• Cancer
• Acute Leukemia
• Chronic Leukemia
• High-Risk Solid Tumors
• Hodgkin & Non-Hodgkin Lymphoma
• Myelodysplastic Syndromes
• Blood Disorders
• Aplastic Anemia
• Beta Thalassemia
• Diamond-Blackfan Anemia
• Fanconi Anemia
• Sickle Cell Disease
• Immune Disorders
o Chronic Granulomatous Disease
o Hystiocytic Disorders
o Leukocyte Adhesion Deficiency
o Severe Combined Immunodeficiency Diseases
o Wiskott-Aldrich Syndrome
• Metabolic Disorders
o Krabbe Disease
o Hurler Syndrome
o Metachromatic Leukodystrophy
o Sanfilippo Syndrome
(For detail list visit parentsguidecordblood.org)
Umbilical Cord
Advertising of the Private Banks
• You only have one chance to collect and store your
baby’s newborn stem cells – immediately after birth.
• After the umbilical cord has been clamped and cut, the
remaining blood in the umbilical cord is drawn into a
collection bag.
• For families opting to bank cord tissue, a section of the
umbilical cord will be collected and stored in the Cord-
Cup Container.
• It’s important to make a decision about saving or donating
well before your due date.
• If you choose to do nothing, your baby’s cord blood and
cord tissue will be discarded as medical waste.
• Newborn stem cells are not embryonic stem cells.
Collecting, storing, and using them is not controversial.
Cord Stem Cells
• There are two primary types of newborn stem cells that have the
potential to be used for different treatments: hematopoietic and
mesenchymal.
• Cord blood predominantly contains hematopoietic stem cells and
cord tissue primarily contains mesenchymal stem cells.
• Mesenchymal stem cells differentiate to build bone, cartilage and
connective tissue, and they are also very effective at mediating the
body’s inflammatory response to damaged or injured cells.
• There have been no clinical trials in humans yet that have used
MSCs derived from cord tissue. However, over 50 studies have used
MSC derived from cord tissue to treat animal models of human
diseases, including: Lung Cancer, Parkinson's Disease, Rheumatoid
Arthritis, Sports injuries to cartilage, and Type 1 Diabetes.
• Also contains immune cells like dendritic cell, regulatory T- cell and
??Monocyte.
Mesenchymal Stem Cells Epithelial and Endothelial
Cells
1 Skeletal disease and injury Wounds, Burns and Ulcers
2 Autoimmune and inflammatory
disease
Ocular surface disease
3 Heart and vascular disease Vascular damage
4 Gastrointestinal disease
5 Cancer
6 Diabetes
7 Transplant Complications
8 Neurological disease and Injury
Cord Blood Cord Tissue
Primary
type of
stem cell
population
Hematopoietic stem cells
(HSCs), which create blood and
immune cells
Mesenchymal stem cells
(MSCs), which create
connective tissue and
bone
Current
therapies
Transplant medicine
Used to treat more than 80
diseases, including various
cancers and blood, immune,
and metabolic disorders†
More than 30,000 cord blood
stem cell transplants performed
worldwide to date.
Currently no proven
therapies, but cord tissue
is being evaluated in
clinical trials as a
therapeutic agent for
optimizing hematopoietic
stem cell transplantation
and in regenerative
medicine i.e. tissue repair.
Cord Blood Cord Tissue
Current
research
Transplant medicine
Hundreds of clinical trials using
cord blood stem cells to help
advance hematopoietic stem cell
transplantation
Regenerative medicine
FDA-regulated clinical trials -
potential treatment for conditions
like cerebral palsy, autism,
traumatic brain injury, and
pediatric stroke.
Laboratory research -
Alzheimer's disease, lung injury,
heart disease, and spinal cord
injury.
Transplant medicine
Ability to minimize
transplant complications
by improving engraftment
rates and reducing the
risk of graft versus host
disease (GVHD).
Regenerative medicine
Clinical trials -
autoimmune disease, liver
disease, orthopedic
indications, and
neurological conditions.
Cord Stem Cell Harvesting
• The method most commonly used in clinical practice is the
“closed technique”, which is similar to standard blood
collection techniques. With this method, the
technician cannulates the vein of the severed umbilical cord
using a needle that is connected to a blood bag, and cord
blood flows through the needle into the bag. On average, the
closed technique enables collection of about 75 ml of cord
blood.
• Collected cord blood is cryopreserved and then stored in
a cord blood bank for future transplantation.
• UCB can be expanded ex vivo over 400-fold by culture
techniques that can block cell differentiation with elimination of
certain components like copper.
• 3 wk treatment with a copper chelator results in preferential
proliferation of a subset of CD34+ cells which seem to be
responsible for expansion in long term culture.
Collection
• Harvesting the tissue of the umbilical cord can yield between
21 million and 500 million MSC.
• A typical cord blood collection in a private bank has a median
CD34+ (HSC) count of 1.6 million.
• Currently there is no standard procedure or accrediting criteria
for storage of MSC from umbilical cord tissue. Many cord
blood banks are storing the cord tissue by freezing an intact
segment of the umbilical cord. This procedure has the
advantage of waiting for the technology of cell separation to
mature, but has the disadvantage that there is no guarantee it
will be possible to efficiently retrieve viable stem cells from a
previously frozen cord.
• A few cord blood banks are extracting stem cells from the cord
tissue before cryogenic storage. This procedure has the
disadvantage that it uses the current separation method, but
the advantage that it yields minimally manipulated cells that
are treatment ready and comply with FDA regulations on cell
therapy products.
Public Vs Private Banking
• A cord blood bank may be private (i.e. the blood is stored
for and the costs paid by donor families) or public (i.e.
stored and made available for use by unrelated donors).
• There are at least 142 public [three in India – Relicord
(Reliance Life) Jeevan Cord and Stemcyte and 25 private
(seven in India) UCB banks worldwide.
• While public cord blood banking is widely supported,
private cord banking is controversial in both the medical
and parenting community.
• Although umbilical cord blood is well-recognized to be
useful for treating hematopoietic and genetic disorders,
some controversy surrounds the collection and storage of
umbilical cord blood by private banks for the baby's use.
• Only a small percentage of babies (estimated at between 1
in 1,000 to 1 in 200,000) ever use the umbilical cord blood
that is stored.
Current Policy
• .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."
• 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.
• Private cord blood banks are usually for-profit organizations
that store cord blood for the exclusive use of the donor or
donor's relatives.
Cord Stem Cell and Transplant
• At one centre, five year Leukemia Free Survival was 40, 42
and 49 per cent with related donors (RD), well matched
unrelated donors (URD) and UCB sources, respectively, while
relapse was 31, 17 and 27 per cent in the same group.
• In May 2006 The World Marrow Donor Association (WMDA)
Policy Statement for the Utility of Autologous or Family Cord
Blood Unit Storage stated that:
• “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.
• There is at present no known protocol where autologous cord
blood stem cells are used in therapy.
• Non- controversial use in some diseases
– Neuroblastoma, Aplastic Anemia
• Controversial in infancy for leukemias
• ALL – Is the clone present at birth??
– Detection of clone Vs Detection of leukemic clone
– Predisposition Vs disease
• AML – Some leukemia specific rearrangements
– E.g. AML/ETO1 found in 35% of Guthrie spots in
children developing AML
• Autologous transplants commonly for adult AML
Metabolic Diseases And Hemoglobinopathies
• In metabolic storage disorders the only therapeutic option is
enzyme replacement therapy which is expensive with a long-
term requirement. Hence, UCB transplant is desirable and a
promising alternative therapeutic option with long term
benefits.
• Prasad et al have reported results of 159 pediatric patients
with inherited metabolic disorders who received UCB
transplant. Engraftment occurred in 87.1 per cent and one
year overall survival was 71.8 per cent.
• Increasing use for Hemoglobinopathies, malignancy and
inherited diseases
– Significantly safer than unrelated donor
– Lower cell dose requirement
– Lower incidence of GvHD
– Improved overall survival
Emerging Therapies- Human Studies
• Cerebral palsy
– Duke “pilot study” is underway
– “A randomized study of autologous umbilical cord
blood Reinfusion in children with cerebral palsy”
• Hydrocephalus
• Hypoxic Ischemic Encephalopathy
– Characterization of cord blood stem cell in situation
of Neonatal Asphyxia – NEOCORD trial
• Hearing loss
• CNS trauma
• Spinal cord injury - Allogeneic
• Cardiovascular trials on
– Ischemic heart disease
– Beurger`s disease
– Congenital heart disease – HLHS
– In strokes
• Immune trials on
– Type 1 Diabetes,
– Rheumatoid Arthritis
– Crohn`s disease
– SLE
– Ulcerative Colitis
– Multiple sclerosis
Our role as Neonatologist
• If a patient requests information on umbilical cord banking,
balanced and accurate information regarding the advantages
and disadvantages of public versus private umbilical cord
blood banking should be provided.
• The remote chance of an autologous unit being used for a
child or a family member (approximately 1 in 2,700
individuals) should be disclosed.
• Discussion may include information regarding maternal
infectious disease and genetic testing, the ultimate outcome of
use of poor quality units of umbilical cord blood, and a
disclosure that demographic data will be maintained on the
patient.
• Directed donation of umbilical cord blood should be
considered when there is a specific diagnosis of a
disease known to be treatable by hematopoietic
transplant for an immediate family member.
• The collection should not alter routine practice for the
timing of umbilical cord clamping.
• Collection of cord blood should be performed after the
delivery of the infant but before delivery of the placenta,
using a closed collection system and procedures that
minimize risk of bacterial and maternal fluid
contamination.
• Physicians or other professionals who recruit pregnant women
and their families for for-profit umbilical cord blood banking
should disclose any financial interests or other potential
conflicts of interest.
• Umbilical cord blood collection should be considered for a
sibling or parent in need of stem cell transplantation when an
HLA-identical bone marrow cell or peripheral stem cell
donation from a sibling or parent is unavailable for
transplantation.
• Umbilical cord blood should be considered when allogeneic
transplantation is the treatment of choice for a child who does
not have an HLA-identical sibling or a well-matched, unrelated
adult bone marrow donor .
• Collection and long-term storage of umbilical cord blood for
autologous donation is not recommended because of the
limited indications and lack of scientific evidence to support
the practice.
The Indian story
• India - high birth rate and genetic diversity.
• Nearly 70 percent of patients of Indian origin who require bone
marrow transplantation do not find a match within their own
family. Hence, unrelated UCB is a widely accepted source of
progenitors for hematopoietic stem cell transplantation.
• However, to-date the total number of UCB transplants
performed in India has been very low mainly due to high cost
and limited number of UCB units available against the
estimated requirement of 30,000 units.
• But with the existence of three public UCB banks these
figures are likely to improve in the coming years.
• Private banks continue to grow in India, as many
families opt to store UCB in private banks with possible
advantages in degenerative disorders in the future.
• To meet the future transplantation needs of the country,
full participation and substantial investment by the
Government is necessary.
THANK YOU

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Stem cell and neonatology vinayak

  • 1. Stem Cell and Neonatology Dr. Vinayak V. Kodur 1st year DM resident L.T.M.General Hospital.
  • 2. Stem Cell History 1998 - Researchers first extract stem cells from human embryos 1999 - First Successful human transplant of insulin-making cells from cadavers 2001 - US President George Bush restricts federal funding for embryonic stem-cell research 2002 - Juvenile Diabetes Research Foundation International creates $20 million fund-raising effort to support stem-cell research 2002 - California ok stem cell research 2004 - Harvard researchers grow stem cells from embryos using private funding
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  • 4. Stem Cell Definition • A cell that has the ability to continuously divide and differentiate (develop) into various other kind(s) of cells/tissues
  • 5. Kinds of Stem Cells Stem cell type Description Examples Totipotent Each cell can develop into a new individual Cells from early (1-3 days) embryos Pluripotent Cells can form any (over 200) cell types Some cells of blastocyst (5 to 14 days) Multipotent Cells differentiated, but can form a number of other tissues Fetal tissue, cord blood, and adult stem cells
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  • 7. Kinds of Stem Cells • Embryonic stem cells come from a five to six-day-old embryo. They have the ability to form virtually any type of cell found in the human body. • Embryonic germ cells are derived from the part of a human embryo or foetus that will ultimately produce eggs or sperm (gametes). • Adult stem cells are undifferentiated cells found among specialized or differentiated cells in a tissue or organ after birth. Based on current research they appear to have a more restricted ability to produce different cell types and to self-renew.
  • 8. Comparison of Stem Cell Sources Umbilical Cord Adult Embryonic 1 Ability to differentiate into various cell types ✓ ✓ ✓ 2 High proliferation capacity ✓ ✓ 3 Low risk of tumor formation ✓ ✓ 4 Low risk of viral contamination ✓ ✓ 5 Capacity for autologous transplantation ✓ ✓ 6 Established/proven treatment in human patients ✓ ✓
  • 9. Cord Blood Stem Cells • Advantage: biologically, a greater degree of human leukocyte antigen mismatch is tolerated by the recipient and the incidence of acute graft-versus-host reaction is decreased when umbilical cord blood is used. • The predominant disadvantage of umbilical cord blood use is related to the low number of stem cells acquired per unit. However, the use of combined units of umbilical cord blood allows for the expansion of umbilical cord blood volume (and increased number of stem cells) to be used for adult hematopoietic transplants. • Studies are currently underway evaluating the feasibility of ex vivo expansion of the units
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  • 17. Few diseases treated with stem cells • Cancer • Acute Leukemia • Chronic Leukemia • High-Risk Solid Tumors • Hodgkin & Non-Hodgkin Lymphoma • Myelodysplastic Syndromes • Blood Disorders • Aplastic Anemia • Beta Thalassemia • Diamond-Blackfan Anemia • Fanconi Anemia • Sickle Cell Disease
  • 18. • Immune Disorders o Chronic Granulomatous Disease o Hystiocytic Disorders o Leukocyte Adhesion Deficiency o Severe Combined Immunodeficiency Diseases o Wiskott-Aldrich Syndrome • Metabolic Disorders o Krabbe Disease o Hurler Syndrome o Metachromatic Leukodystrophy o Sanfilippo Syndrome (For detail list visit parentsguidecordblood.org)
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  • 22. Advertising of the Private Banks • You only have one chance to collect and store your baby’s newborn stem cells – immediately after birth. • After the umbilical cord has been clamped and cut, the remaining blood in the umbilical cord is drawn into a collection bag. • For families opting to bank cord tissue, a section of the umbilical cord will be collected and stored in the Cord- Cup Container. • It’s important to make a decision about saving or donating well before your due date. • If you choose to do nothing, your baby’s cord blood and cord tissue will be discarded as medical waste. • Newborn stem cells are not embryonic stem cells. Collecting, storing, and using them is not controversial.
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  • 24. Cord Stem Cells • There are two primary types of newborn stem cells that have the potential to be used for different treatments: hematopoietic and mesenchymal. • Cord blood predominantly contains hematopoietic stem cells and cord tissue primarily contains mesenchymal stem cells. • Mesenchymal stem cells differentiate to build bone, cartilage and connective tissue, and they are also very effective at mediating the body’s inflammatory response to damaged or injured cells. • There have been no clinical trials in humans yet that have used MSCs derived from cord tissue. However, over 50 studies have used MSC derived from cord tissue to treat animal models of human diseases, including: Lung Cancer, Parkinson's Disease, Rheumatoid Arthritis, Sports injuries to cartilage, and Type 1 Diabetes. • Also contains immune cells like dendritic cell, regulatory T- cell and ??Monocyte.
  • 25. Mesenchymal Stem Cells Epithelial and Endothelial Cells 1 Skeletal disease and injury Wounds, Burns and Ulcers 2 Autoimmune and inflammatory disease Ocular surface disease 3 Heart and vascular disease Vascular damage 4 Gastrointestinal disease 5 Cancer 6 Diabetes 7 Transplant Complications 8 Neurological disease and Injury
  • 26. Cord Blood Cord Tissue Primary type of stem cell population Hematopoietic stem cells (HSCs), which create blood and immune cells Mesenchymal stem cells (MSCs), which create connective tissue and bone Current therapies Transplant medicine Used to treat more than 80 diseases, including various cancers and blood, immune, and metabolic disorders† More than 30,000 cord blood stem cell transplants performed worldwide to date. Currently no proven therapies, but cord tissue is being evaluated in clinical trials as a therapeutic agent for optimizing hematopoietic stem cell transplantation and in regenerative medicine i.e. tissue repair.
  • 27. Cord Blood Cord Tissue Current research Transplant medicine Hundreds of clinical trials using cord blood stem cells to help advance hematopoietic stem cell transplantation Regenerative medicine FDA-regulated clinical trials - potential treatment for conditions like cerebral palsy, autism, traumatic brain injury, and pediatric stroke. Laboratory research - Alzheimer's disease, lung injury, heart disease, and spinal cord injury. Transplant medicine Ability to minimize transplant complications by improving engraftment rates and reducing the risk of graft versus host disease (GVHD). Regenerative medicine Clinical trials - autoimmune disease, liver disease, orthopedic indications, and neurological conditions.
  • 28. Cord Stem Cell Harvesting • The method most commonly used in clinical practice is the “closed technique”, which is similar to standard blood collection techniques. With this method, the technician cannulates the vein of the severed umbilical cord using a needle that is connected to a blood bag, and cord blood flows through the needle into the bag. On average, the closed technique enables collection of about 75 ml of cord blood. • Collected cord blood is cryopreserved and then stored in a cord blood bank for future transplantation. • UCB can be expanded ex vivo over 400-fold by culture techniques that can block cell differentiation with elimination of certain components like copper. • 3 wk treatment with a copper chelator results in preferential proliferation of a subset of CD34+ cells which seem to be responsible for expansion in long term culture.
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  • 32. • Harvesting the tissue of the umbilical cord can yield between 21 million and 500 million MSC. • A typical cord blood collection in a private bank has a median CD34+ (HSC) count of 1.6 million. • Currently there is no standard procedure or accrediting criteria for storage of MSC from umbilical cord tissue. Many cord blood banks are storing the cord tissue by freezing an intact segment of the umbilical cord. This procedure has the advantage of waiting for the technology of cell separation to mature, but has the disadvantage that there is no guarantee it will be possible to efficiently retrieve viable stem cells from a previously frozen cord. • A few cord blood banks are extracting stem cells from the cord tissue before cryogenic storage. This procedure has the disadvantage that it uses the current separation method, but the advantage that it yields minimally manipulated cells that are treatment ready and comply with FDA regulations on cell therapy products.
  • 33. Public Vs Private Banking • A cord blood bank may be private (i.e. the blood is stored for and the costs paid by donor families) or public (i.e. stored and made available for use by unrelated donors). • There are at least 142 public [three in India – Relicord (Reliance Life) Jeevan Cord and Stemcyte and 25 private (seven in India) UCB banks worldwide. • While public cord blood banking is widely supported, private cord banking is controversial in both the medical and parenting community. • Although umbilical cord blood is well-recognized to be useful for treating hematopoietic and genetic disorders, some controversy surrounds the collection and storage of umbilical cord blood by private banks for the baby's use. • Only a small percentage of babies (estimated at between 1 in 1,000 to 1 in 200,000) ever use the umbilical cord blood that is stored.
  • 34. Current Policy • .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." • 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. • Private cord blood banks are usually for-profit organizations that store cord blood for the exclusive use of the donor or donor's relatives.
  • 35. Cord Stem Cell and Transplant • At one centre, five year Leukemia Free Survival was 40, 42 and 49 per cent with related donors (RD), well matched unrelated donors (URD) and UCB sources, respectively, while relapse was 31, 17 and 27 per cent in the same group. • In May 2006 The World Marrow Donor Association (WMDA) Policy Statement for the Utility of Autologous or Family Cord Blood Unit Storage stated that: • “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. • There is at present no known protocol where autologous cord blood stem cells are used in therapy.
  • 36. • Non- controversial use in some diseases – Neuroblastoma, Aplastic Anemia • Controversial in infancy for leukemias • ALL – Is the clone present at birth?? – Detection of clone Vs Detection of leukemic clone – Predisposition Vs disease • AML – Some leukemia specific rearrangements – E.g. AML/ETO1 found in 35% of Guthrie spots in children developing AML • Autologous transplants commonly for adult AML
  • 37. Metabolic Diseases And Hemoglobinopathies • In metabolic storage disorders the only therapeutic option is enzyme replacement therapy which is expensive with a long- term requirement. Hence, UCB transplant is desirable and a promising alternative therapeutic option with long term benefits. • Prasad et al have reported results of 159 pediatric patients with inherited metabolic disorders who received UCB transplant. Engraftment occurred in 87.1 per cent and one year overall survival was 71.8 per cent. • Increasing use for Hemoglobinopathies, malignancy and inherited diseases – Significantly safer than unrelated donor – Lower cell dose requirement – Lower incidence of GvHD – Improved overall survival
  • 38. Emerging Therapies- Human Studies • Cerebral palsy – Duke “pilot study” is underway – “A randomized study of autologous umbilical cord blood Reinfusion in children with cerebral palsy” • Hydrocephalus • Hypoxic Ischemic Encephalopathy – Characterization of cord blood stem cell in situation of Neonatal Asphyxia – NEOCORD trial • Hearing loss • CNS trauma • Spinal cord injury - Allogeneic
  • 39. • Cardiovascular trials on – Ischemic heart disease – Beurger`s disease – Congenital heart disease – HLHS – In strokes • Immune trials on – Type 1 Diabetes, – Rheumatoid Arthritis – Crohn`s disease – SLE – Ulcerative Colitis – Multiple sclerosis
  • 40. Our role as Neonatologist • If a patient requests information on umbilical cord banking, balanced and accurate information regarding the advantages and disadvantages of public versus private umbilical cord blood banking should be provided. • The remote chance of an autologous unit being used for a child or a family member (approximately 1 in 2,700 individuals) should be disclosed. • Discussion may include information regarding maternal infectious disease and genetic testing, the ultimate outcome of use of poor quality units of umbilical cord blood, and a disclosure that demographic data will be maintained on the patient.
  • 41. • Directed donation of umbilical cord blood should be considered when there is a specific diagnosis of a disease known to be treatable by hematopoietic transplant for an immediate family member. • The collection should not alter routine practice for the timing of umbilical cord clamping. • Collection of cord blood should be performed after the delivery of the infant but before delivery of the placenta, using a closed collection system and procedures that minimize risk of bacterial and maternal fluid contamination.
  • 42. • Physicians or other professionals who recruit pregnant women and their families for for-profit umbilical cord blood banking should disclose any financial interests or other potential conflicts of interest. • Umbilical cord blood collection should be considered for a sibling or parent in need of stem cell transplantation when an HLA-identical bone marrow cell or peripheral stem cell donation from a sibling or parent is unavailable for transplantation. • Umbilical cord blood should be considered when allogeneic transplantation is the treatment of choice for a child who does not have an HLA-identical sibling or a well-matched, unrelated adult bone marrow donor . • Collection and long-term storage of umbilical cord blood for autologous donation is not recommended because of the limited indications and lack of scientific evidence to support the practice.
  • 43. The Indian story • India - high birth rate and genetic diversity. • Nearly 70 percent of patients of Indian origin who require bone marrow transplantation do not find a match within their own family. Hence, unrelated UCB is a widely accepted source of progenitors for hematopoietic stem cell transplantation. • However, to-date the total number of UCB transplants performed in India has been very low mainly due to high cost and limited number of UCB units available against the estimated requirement of 30,000 units. • But with the existence of three public UCB banks these figures are likely to improve in the coming years.
  • 44. • Private banks continue to grow in India, as many families opt to store UCB in private banks with possible advantages in degenerative disorders in the future. • To meet the future transplantation needs of the country, full participation and substantial investment by the Government is necessary.