Publications by authors named "Ilham Saleh Abuljadayel"

Background & Objectives: Aplastic anaemia is a life threatening rare bone marrow failure disorder. The underlying haematopoietic cellular deficit leads to haemorrhage, infection and severe anaemia. The treatment of choice for this haematological condition is allogeneic bone marrow transplantation from fully matched HLA sibling.

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Processes involving conversion of mature adult cells into undifferentiated cells have tremendous therapeutic potential in treating a variety of malignant and non-malignant disorders, including degenerative diseases. This can be achieved in autologous or allogeneic settings, by replacing either defective cells or regenerating those that are in deficit through reprogramming more committed cells into stem cells. The concept behind reprogramming differentiated cells to a stem cell state is to enable the switching of development towards the required cell lineage that is capable of correcting the underlying cellular dysfunction.

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Article Synopsis
  • - Beta-thalassemia is a genetic disorder that leads to reduced red blood cell lifespan and severe anemia due to an imbalance in hemoglobin chains, primarily affecting the adult beta-globin chain.
  • - Current treatments include regular blood transfusions and chelation therapy to manage iron overload, with newer strategies exploring fetal hemoglobin switching to improve red blood cell survival.
  • - In a study involving 21 beta-thalassemia patients, autologous retrodifferentiated stem cell infusions significantly reduced transfusion needs, increased fetal hemoglobin production, and improved various blood parameters over a six-month period.
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Undifferentiated pluripotent stem cells with flexible developmental potentials are not normally found in peripheral blood. However, such cells have recently been reported to reside in the bone marrow. Herein are reported methods of inducing pluripotency in cells derived from unmobilised adult human peripheral blood.

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