TY - JOUR
T1 - Concise review
T2 - Stem cell-based approaches to red blood cell production for transfusion
AU - Shah, Siddharth
AU - Huang, Xiaosong
AU - Cheng, Linzhao
PY - 2014
Y1 - 2014
N2 - Blood transfusion is a common procedure in modern medicine, and it is practiced throughout the world; however, many countries report a less than sufficient blood supply. Even in developed countries where the supply is currently adequate, projected demographics predict an insufficient supply as early as 2050. The blood supply is also strained during occasional widespread disasters and crises. Transfusion of blood components such as red blood cells (RBCs), platelets, or neutrophils is increasingly used from the same blood unit for multiple purposes and to reduce alloimmune responses. Even for RBCs and platelets lacking nuclei and many antigenic cell-surface molecules, alloimmunity could occur, especially in patients with chronic transfusion requirements. Once alloimmunization occurs, such patients require RBCs from donors with a different blood group antigen combination, making it a challenge to find donors after every successive episode of alloimmunization. Alternative blood substitutes such as synthetic oxygen carriers have so far proven unsuccessful. In this review, we focus on current research and technologies that permit RBC production ex vivo from hematopoietic stem cells, pluripotent stem cells, and immortalized erythroid precursors.
AB - Blood transfusion is a common procedure in modern medicine, and it is practiced throughout the world; however, many countries report a less than sufficient blood supply. Even in developed countries where the supply is currently adequate, projected demographics predict an insufficient supply as early as 2050. The blood supply is also strained during occasional widespread disasters and crises. Transfusion of blood components such as red blood cells (RBCs), platelets, or neutrophils is increasingly used from the same blood unit for multiple purposes and to reduce alloimmune responses. Even for RBCs and platelets lacking nuclei and many antigenic cell-surface molecules, alloimmunity could occur, especially in patients with chronic transfusion requirements. Once alloimmunization occurs, such patients require RBCs from donors with a different blood group antigen combination, making it a challenge to find donors after every successive episode of alloimmunization. Alternative blood substitutes such as synthetic oxygen carriers have so far proven unsuccessful. In this review, we focus on current research and technologies that permit RBC production ex vivo from hematopoietic stem cells, pluripotent stem cells, and immortalized erythroid precursors.
KW - Erythropoiesis
KW - Hematopoietic stem cells
KW - Pluripotent stem cells
KW - Red blood cell transfusion
KW - Reticulocytes
UR - http://www.scopus.com/inward/record.url?scp=84896275082&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84896275082&partnerID=8YFLogxK
U2 - 10.5966/sctm.2013-0054
DO - 10.5966/sctm.2013-0054
M3 - Review article
C2 - 24361925
AN - SCOPUS:84896275082
SN - 2157-6564
VL - 3
SP - 346
EP - 355
JO - Stem cells translational medicine
JF - Stem cells translational medicine
IS - 3
ER -