Children born with severe combined immunodeficiency treated with genetically altered HIV
Thursday, 18 April 2019
Human Immunodeficiency Virus (HIV) has been used to make a gene therapy that seems to have cured eight infants of severe combined immunodeficiency (SCID-X1), or “Bubble Boy” disease.
David Vetter, was perhaps the most famous patient with severe combined immunodeficiency (SCID), which made it impossible for him to engage with the world outside a plastic chamber. His parents had already lost one child to the disease before he was born. Within 20 seconds of his birth in 1971 at the Texas Children’s Hospital in Houston, he was placed in a plastic isolation chamber, where he lived until the age of six when he was given a special plastic suit designed by NASA, the US space agency.
Nicknamed “Bubble Boy”, Vetter died at the age of 12 after a failed bone marrow transplant.
Results of the latest research*, developed at a Tennessee hospital, were published in the New England Journal of Medicine. Doctors report that the babies, born with little to no immune protection, now have fully functional immune systems. Untreated babies with this disorder have to live in completely sterile conditions and tend to die as infants.
The gene therapy involved collecting the babies’ bone marrow and correcting the genetic defect in their DNA soon after their birth. The “correct” gene – used to fix the defect – was inserted into an altered version of one of HIV, the virus that causes AIDS.
Researchers said most of the babies were discharged from the hospital within one month.
Dr Ewelina Mamcarz of St Jude Children’s Research Hospital in Memphis, an author of the study, said in a statement: “These patients are toddlers now, who are responding to vaccinations and have immune systems to make all immune cells they need for protection from infections as they explore the world and live normal lives.”
“This is a first for patients with SCID-X1,” she added, referring to the most common type of SCID.
The patients were treated at St Jude’s and at UCSF Benioff Children’s Hospital in San Francisco.
Currently, the best treatment for SCID-XI is a bone marrow transplant with a tissue-matched sibling donor. But according to St Jude, more than 80% of these patients lack such donors and must rely on blood stem cells from other donors. This process is less likely to cure the “Bubble Boy” disease and is more likely to cause serious side effects as a result of treatment.
Previous advancements in gene therapy provided alternatives to a bone marrow transplant, but these treatments sometimes involved chemotherapy and had implications for a range of other diseases, including blood disorders, sickle cell anaemia and thalassaemia, and metabolic syndrome.
*Mamcarz E, Zhou S, Lockey T, et al. Lentiviral Gene Therapy Combined with Low-Dose Busulfan in Infants with SCID-X. N Engl J Med 2019; 380:1525-1534. April 18, 2019. DOI: 10.1056/NEJMoa1815408
Source link : http://www.onmedica.com/newsArticle.aspx?id=9269b83f-4a21-41a3-a944-8bc3d1fff46f
Publish date : 2019-04-18 10:21:44