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Gene Therapy for Netherton Syndrome

Phase 1
Conditions
Netherton Syndrome
Interventions
Genetic: One 20cm2/10cm2 autologous skin sheet graft
Registration Number
NCT01545323
Lead Sponsor
Great Ormond Street Hospital for Children NHS Foundation Trust
Brief Summary

Netherton Syndrome is a serious skin disorder caused by damage in a gene called SPINK5. This gene controls the formation of a protein called LEKTI, which important for skin barrier function. LEKTI inhibits certain enzymes (serine proteinases) in the outermost layer of the skin (epidermis). The function of the serine proteinases is to break down the intracellular cement that holds together the horny cells in the epidermis, in order for the skin to be able to shed cells (known as cell desquamation). LEKTI deficiency leads to an uninhibited desquamation of horny cells, and as a result the skin becomes red and scaly. The barrier function of the skin is also affected. The permeability of the skin increases, and its capacity to bind water decreases, which causes dryness. The thinness of the barrier also results in over absorption of chemicals, for example topical medical treatments. Historically one in ten infants dies before their first birthday. Currently there are no proven treatments to cure this condition.

The investigators have been developing a gene therapy approach to treat this disorder. The investigators have used a disabled virus (vector) to carry a functional copy of the SPINK5 gene into skin stem cells. Proof-of-principle experiments have shown the investigators can restore almost normal shape and size of the upper layer of the skin in skin grafts grown in the lab. Even if only a small number of cells are genetically modified to carry the corrected SPINK5 gene, there seems to be a correction over a wide area of the graft.

In this trial the investigators propose grafting of autologous epidermal sheets generated from genetically modified skin stem cells for the treatment of patients with Netherton Syndrome. The investigators anticipate production and release of LEKTI protein from even a small patch of skin will be beneficial.

Detailed Description

Netherton Syndrome is a serious skin disorder caused by damage in a gene called SPINK5. This gene controls the formation of a protein called LEKTI, which important for skin barrier function. LEKTI inhibits certain enzymes (serine proteinases) in the outermost layer of the skin (epidermis). The function of the serine proteinases is to break down the intracellular cement that holds together the horny cells in the epidermis, in order for the skin to be able to shed cells (known as cell desquamation). LEKTI deficiency leads to an uninhibited desquamation of horny cells, and as a result the skin becomes red and scaly. The barrier function of the skin is also affected. The permeability of the skin increases, and its capacity to bind water decreases, which causes dryness. The thinness of the barrier also results in over absorption of chemicals, for example topical medical treatments. Historically one in ten infants dies before their first birthday. Currently there are no proven treatments to cure this condition.

The investigators have been developing a gene therapy approach to treat this disorder. The investigators have used a disabled virus (vector) to carry a functional copy of the SPINK5 gene into skin stem cells. Proof-of-principle experiments have shown the investigators can restore almost normal shape and size of the upper layer of the skin in skin grafts grown in the lab. Even if only a small number of cells are genetically modified to carry the corrected SPINK5 gene, there seems to be a correction over a wide area of the graft.

In this trial the investigators propose grafting of autologous epidermal sheets generated from genetically modified skin stem cells for the treatment of patients with Netherton Syndrome. The investigators anticipate production and release of LEKTI protein from even a small patch of skin will be beneficial.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
5
Inclusion Criteria
  • Confirmed SPINK5 mutations in both alleles by direct DNA sequencing
  • Absence of LEKTI protein expression in the skin by in situ immunostaining
  • Patient informed consent, or parental/guardian consent in the case of minor participant
Exclusion Criteria
  • History of skin malignancy or evidence of current active malignant skin disease
  • Pregnancy
  • Hepatitis A, B, C or HIV positive
  • Current antibiotic resistant bacterial colonisation

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
One 20cm2/10cm2 autologous skin sheet graftOne 20cm2/10cm2 autologous skin sheet graftAdults will receive a graft of approximately 20cm2. Children under 16 years of age will receive a graft around half this size, around 10cm2 .The graft is derived from SPINK5 transduced cells
Primary Outcome Measures
NameTimeMethod
Safety of gene modified grafts1 year

Adverse events will be monitored and assessed throughout the duration of the trial. Patients will be followed-up on-trial for 1 year. Subsequently, patients will be followed-up off-trial for life, as part of normal clinical care.

Histological evidence of correction of graft skin architecture1 year

A skin biopsy will be taken from the graft area to determine correction of the skin architecture and to identify expression of LEKTI at time points 1, 3, 6 \& 12 months post-grafting.

Secondary Outcome Measures
NameTimeMethod
Detection of increased LEKT1 staining at site outside the graft1 year

A skin biopsy will be taken from the graft area to enable LEKTI staining at time points 1, 3, 6 \& 12 months post-grafting.

Immune response to graft/transgene1 year

ELISPOT will be used to detect possible cell mediated responses against the gene modified graft at time points 1, 3, 6 \& 12 months post-grafting.

Trial Locations

Locations (2)

Guy's and St Thomas NHS Trust

🇬🇧

London, United Kingdom

Great Ormond Street Hospital for Children NHS Trust

🇬🇧

London, United Kingdom

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