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Gene Therapy Trials for PID:A Nursing Perspective Jin Hua Xu-Bayford Clinical Nurse Specialist Gene Therapy Email: xuj@gosh.nhs.uk The child first and always
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Outline of talk What is Gene Therapy Gene Therapy trials at GOSH What are the procedures Entry criteria Ethical/Safety Issues Preparation of the family Post gene therapy follow up monitoring
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Gene Therapy Advisory Committee (GTAC) definition of Gene Therapy "The deliberate introduction of genetic material into human somatic cells for therapeutic, prophylactic or diagnostic purposes."
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Two Types of Gene Therapy Somatic gene therapy involves introducing a “good “ gene into targeted cells with the end results of treating the patient-not the future children Germline gene therapy involves modifying the genes in egg or sperm cells, which will then pass any genetic changes to future generations as well
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Trials under taken at GOSH X-Linked Severe Combined Immunodeficiency (SCID-X1), now it is closed Adenosine Deaminase Deficiency (ADA- SCID) X-Linked Chronic Granulomatous Disease (X-CGD)
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Entry criteria for the trials
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Trial Entry Criteria for SCID-X1 Molecularly confirmed diagnosis No MSD, MFD or fully matched MUD GTAC approval Parental/guardian voluntary consent
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Entry Criteria for X-CGD Molecularly Confirmed diagnosis X-CGD At least one severe infection needing hospital treatment, or sever inflammation due to CGD No MSD, MFD or fully matched MUD GTAC approval Parental/guardian voluntary consent
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Entry criteria trial for ADA Molecularly Confirmed diagnosis of ADA- SCID Failure of PEG-ADA No HLA identical family donor GTAC approval Parental/guardian voluntary consent
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How parents choose GT vs BMT Percentage of survival following gene therapy is greater than following a MUD SCT. Fear of chemotherapy Fertility issues for the child Shorter hospitalisation with gene therapy Safer treatment, at least in the short term
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Decision making GT remains a largely experimental and innovative treatment Currently undergoing clinical trials with PID One centre in the UK is treating Children using this form of therapy Rapidly expanding field Media attraction / publicity
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Preparation of the family Begins once a diagnosis of ADA or X-linked SCID has been established Tissue typing for family to search a MFD Medical team approaching GTAC-seek approval for gene therapy Consultation with immunology and BMT consultants Independent consultation
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Other factors Availability of the vector Laboratory resources to prepare the cells Theatre space for the child to have a bone marrow harvest Availability of UCLH laboratory for CD34 selection Availability of a bed on the appropriate unit
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Administration of Gene Transduced cells Apply principles of BM/ PBSC infusion Via blood giving set Over 30-40 minutes Ensure appropriate cover prescribed( Chlorphenamine & Hydrocortisone) Less likely to react as own cells given back Usually on a Friday afternoon
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Patients treated at GOSH X-SCID (10 patients) ADA SCID (3 patient) X-CGD (2 patients)
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Immune reconstitution post gene therapy 4-6 weeks, natural killer (NK) cells start recovering Approx 12 weeks, T-cells start recovering Approx 6 months, CD4 should be reaching 300
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Risks and side effects of Gene Therapy 3 Paris patients developed T cell Leukaemia 2/3 were the youngest patients (<3 months) 2 patients in remission and 1 died
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Ethical / Safety Issues GTAC - Gene Therapy Advisory Committee Not germ line (eggs and sperm) gene therapy -only somatic cells (body cells) are corrected Theoretical risk of harm from virus Risk of malignancy- insertional mutagenesis DoH health record flagging Informed consent Unknown risks as novel procedure
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Parental Support Numbers of children being treated remain very small Parents support parents MDT offer information and support Medical and nursing experiences
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Balancing clinical risk and benefit
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6th October 2006
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