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Centre de recherche
Thursday, November 15 2018
Press release

Treating the "bubble babies"

An international study led by Montreal researchers finds better ways to improve the chances of survival of children with a rare immune deficiency

MONTREAL, November 15, 2018 – An international study published in the journal Blood by researchers led by Dr. Elie Haddad, a pediatric immunologist and researcher at CHU Sainte-Justine and professor at Université de Montréal, highlights the urgent need to develop better treatment strategies for patients suffering from severe combined immune deficiency (SCID).

This deficiency, better known as "bubble baby disease" is a rare syndrome characterized by a total non-function of the body’s immune system. The children affected have no immune defence and are vulnerable to bacteria, viruses and fungi, resulting in repeated severe infections. Without appropriate treatment, in most cases this disease is fatal within the first months after birth.

SCID can be caused by mutations in various genes involved in the functioning of the immune system. The new research shows that the nature of the mutated gene (or genotype) has a significant influence on patients’ survival and reconstitution of their immune system after bone marrow transplant. According to the study, the genotype must be taken into account when adapting treatment strategies to individual patients.

44 Medical Centres Involved

Funded by the U.S. National Institutes of Health, the Primary Immune Deficiency Treatment Consortium (PIDTC) involves 44 medical centres across North America. The PIDTC conducted a retrospective analysis of 662 patients with SCID who received hematopoietic stem cell transplants as their first therapy between 1982 and 2012 in 33 of these centres, forming the basis of the new study.

"Immune diseases are among the top priorities at CHU Sainte-Justine in terms of care, teaching and research,” Haddad said. “There are only one or two cases of SCID per year in Quebec. Having access to such a cohort of patients with this rare disease and over such a long period has provided us with significant and unique data to advance our knowledge in this area.”

The results showed that survival rates of patients were higher after a cell transplant from a matched sibling donor. In recipients from other donor types, which represent 86 per cent of cases, the data showed that the SCID genotype had a strong influence on survival and immune reconstitution. In addition, the researchers found that young age and absence of active infection at the time of transplant were also key factors for survival, and both were significantly associated with improved survival following a transplant.

Critical Need for Neonatal Screening

"We need to develop patient-specific treatment strategies,” Haddad said. “There is a critical need for neonatal screening to establish appropriate isolation, implement infection-prevention measures, particularly before transplantation, and ensure rapid referral for bone-marrow transplant or gene therapy after diagnosis.”

The study also points to the need for close monitoring of immune-system reconstitution after treatment to identify patients with conditions that may require additional intervention and prevent a poor long-term prognosis. Further studies will be needed to identify patient- and transplant-related factors that limit early immune-system reconstitution, and to determine the most appropriate and effective interventions.

"In our future research, our objective will be to analyze the late effects of conditioning and the quality of long-term immune-system reconstitution after hematopoietic cell transplant for this deficiency," said Haddad.

About the Study

"SCID genotype and 6-month post-transplant CD4 count predict survival and immune recovery," by Elie Haddad, Hélène Decaluwe, Pierre Teira et al., was published in the prestigious journal Blood on Oct. 25, 2018. The article was selected as a "plenary paper," i.e. a study of major scientific importance, and is accompanied by an editorial. Dr. Haddad is a clinician-scientist in clinical immunology at CHU Sainte-Justine and a full professor in the Department of Pediatrics at Université de Montréal; he is also a member of the steering committee of the Primary Immune Deficiency Treatment Consortium. Drs. Hélène Decaluwe, Fabien Touzot and Pierre Teira are among the clinicians at CHU Sainte-Justine also involved in the consortium, which is funded by the U.S. National Institutes of Health.

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About the CHU Sainte-Justine Research Center

The Center is part of the CHU Sainte-Justine, the largest mother-child center in Canada and second largest pediatric center in North America. The CHU Sainte-Justine Research Center is a leading mother-child research institution affiliated with Université de Montréal. Focused on the discovery of innovative prevention methods, less intrusive and faster treatments and promising avenues for personalized medicine, it brings together more than 200 researchers, including more than 90 clinical researchers, as well as over 500 graduate and postdoctoral students. For more information, go to research.chusj.org.

Source
CHU Sainte-Justine
Contact

Maude Hoffmann
Communications advisor, CHU Sainte-Justine Research Center
communications@recherche-ste-justine.qc.ca

Media contacts:

Florence Meney
Office: 514-345-4931, ext. 7707
florence.meney.hsj@ssss.gouv.qc.ca

Patsy Coulanges
Office: 514-345-4931, ext. 4354
patsy.coulanges.hsj@ssss.gouv.qc.ca

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Updated on 11/15/2018
Created on 11/15/2018
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