Twenty-Five Years of Gene Therapy for ADA-SCID: From Bubble Babies to an Approved Drug

Francesca Ferrua1,2, Alessandro Aiuti1,2

  • 11 San Raffaele Telethon Institute for Gene Therapy (SR-Tiget), Pediatric Immunohematology and Bone Marrow Transplantation Unit, San Raffaele Scientific Institute , Milan, Italy.

Human Gene Therapy
|August 30, 2017
PubMed

Insights

Gene therapy for adenosine deaminase-SCID (ADA-SCID) has evolved over 25 years, offering a safe and effective treatment. This approach corrects the genetic defect, restoring immune function and improving patient outcomes.

Area of Science:

  • Immunology
  • Genetics
  • Pediatrics

Background:

  • Severe combined immunodeficiency (SCID) due to adenosine deaminase (ADA) deficiency is a fatal genetic disorder.
  • Hematopoietic stem cell (HSC) transplant is curative but limited; enzyme replacement therapy has drawbacks.
  • Gene therapy (GT) offers a promising alternative for ADA-SCID treatment.

Purpose of the Study:

  • To review 25 years of gene therapy development for ADA-SCID.
  • To highlight advancements in vector technology and patient outcomes.
  • To discuss the safety and efficacy of ADA-SCID gene therapy.

Main Methods:

  • Early studies used gamma-retroviral vectors for gene correction of lymphocytes and HSCs.
  • Introduction of low-intensity conditioning improved HSC engraftment.
  • Lentiviral vectors have also been employed in recent clinical trials.

Main Results:

  • Gamma-retroviral gene therapy shows a favorable safety profile with sustained efficacy over 13 years.
  • No abnormal clonal proliferation or leukemia observed in over 40 treated patients.
  • Marketing approval for Strimvelis™ in 2016 marked a significant milestone.

Conclusions:

  • Gene therapy has significantly improved ADA-SCID patient prognosis.
  • Advances in gene therapy contribute to broader applications beyond inherited diseases.
  • Newborn screening aids in earlier diagnosis and treatment initiation.