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Table 1 Non-Malignant Disorders Treated With Cord Blood

From: Cord blood in regenerative medicine: do we need immune suppression?

Disorder

Number Treated

Outcome

Ref.

Hurler's syndrome

20

17 of the 20 children were alive a median of 905 days after transplantation, with complete donor chimerism and normal peripheral-blood alpha-L-iduronidase activity

[100]

Duchenne muscular dystrophy

1

On 42nd day, physical examination revealed obviously improvement in walking, turning the body over, and standing up

[101]

Malignant infantile osteopetrosis

1

Normalization of spine bone mineral density.

[102]

Rothmund-Thomson syndrome

1

Complete immune reconstitution

[55]

Buerger's disease

4

Ischemic rest pain suddenly disappeared. Digital capillaries were increased in number and size.

[84]

Spinal Cord Injury

1

Improved sensory perception and movement in the SPI patient's hips and thighs within 41 days of cell transplantation. Regeneration of the spinal cord at the injured site

[85]

Krabbe's disease

25

Progressive central myelination and continued gains in developmental skills, and most had age-appropriate cognitive function and receptive language skills in patient subset

[14]

Omenn syndrome

1

T cell reconstitution

[103]

Non-healing wounds

2

Accelerated healing

[86]

Refractory anemia

3

All patients are alive and free of disease at between 17 and 39 months after cord blood administration

[104]

Diamond-Blackfan anemia

1

Successful seroconversion to vaccines (diphtheria, pertussis, tetanus, rubella, measles, and BCG) administered 22–34 months post-transplant.

[105]

Severe chronic active Epstein-Barr virus

1

Complete remission without circulating EBV-DNA has continued for 15 months transplant.

[106]

Behcet's disease

1

Twenty-three months after CBT, the patient is doing well and has no signs or symptoms of Behcet's disease

[9]

Mucopolysaccharidosis type IIB (Hunter syndrome)

1

Two years after transplant approximately 55% normal plasma iduronate sulfatase. activity has been restored and abnormal urinary excretion of glycosaminoglycans has nearly completely resolved.

[107]