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CCR5Δ32 cord blood stem cells refers to a therapeutic approach using umbilical cord blood-derived hematopoietic stem cells from donors who are homozygous for the CCR5Δ32 mutation. This cell therapy strategy is used to treat patients with HIV-1 and concurrent hematologic malignancies, such as acute myeloid leukemia, who require hematopoietic stem cell transplantation. The CCR5Δ32 mutation is a 32-base pair deletion in the CCR5 gene that results in a non-functional CCR5 co-receptor, which is the primary entry point for most HIV-1 strains into CD4+ T cells. By replacing the patient's immune system with these resistant cells, the therapy aims to achieve long-term HIV remission or a cure. Research has been led by institutions such as Weill Cornell Medicine and the IMPAACT network, utilizing cord blood units screened by banks like StemCyte.
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