Study to Understand the Genetic Risk of Developing an Immune Response After Blood Transfusions Among Individuals With Sickle Cell Disease
Recruiting · NCT06944067 · Observational (researchers observe without assigning treatment) · Lead sponsor: National Human Genome Research Institute (NHGRI)
View the official record on ClinicalTrials.gov →What this trial is about
The purpose of this research study is to look at genes and determine how they interact with each other to find changes that could explain why some people's immune systems may respond to blood transfusions. This response is called an alloimmune response. We strongly believe that when someone has an alloimmune response, it is caused by changes in their genes. We plan to compare changes in the genes of individuals that develop red blood cell alloimmunization after blood transfusions with those that do not develop alloimmunization. This may help us to create more targeted therapeutic interventions, which may improve the health of alloimmune responders.
Who can take part
Inclusion criteria
- To be eligible to participate in this study, an individual must meet all of the following criteria:
- \. Individual (\> 2 years of age) with confirmed SCD diagnosis who meets at least one of the following conditions:
- History of greater than ten administered transfusions or 20 transfusion units (where known)
- History of one or more antibody screens
- Known candidate variant genotype
Exclusion criteria
- An individual who meets any the following criteria will be excluded from participation in this study:
- Impaired decision-making capability, with or without a legally authorized representative
- History of transplant (e.g., organ, bone marrow, stem cell)
- Taking immunosuppressive medications at time of enrollment
- Confirmed pregnancy
Where it is running
1 location listed across 1 US state.
- National Institutes of Health Clinical Center - Bethesda, Maryland, United States