University of Glasgow, UK.
Br J Haematol. 2010 Apr;149(1):22-34. doi: 10.1111/j.1365-2141.2010.08079.x. Epub 2010 Feb 11.
Whilst red cell transfusion is a well established cellular therapy, the problems of insufficiency of supply, transfusion transmitted infections and the requirement for immunological matching persist. The possibility of generating large numbers of O Rh D negative red cells at Good Manufacturing Practice grade as a route to circumvent these issues is therefore an attractive proposition. Significant numbers of erythrocytes can be generated from somatic haematopoietic stem cells, but it seems unlikely that these can provide sufficient volumes for large scale manufacture. However, human embryonic stem cells (hESC) and, potentially, induced pluripotent stem cells (iPSC), may provide a route to this objective. Red cell transfusion is an attractive goal for pluripotent stem cell-derived therapeutics because it is a well-characterised single cell suspension that lacks nucleated cells and has a low expression of human leucocyte antigen molecules, but many challenges remain in translating this cellular therapy to the clinic.
虽然红细胞输注是一种成熟的细胞疗法,但供应不足、输血传播感染和免疫匹配的问题仍然存在。因此,作为一种规避这些问题的途径,以良好生产规范(GMP)级别生成大量 O 型 RhD 阴性红细胞的可能性是一个诱人的提议。大量的红细胞可以从体造血干细胞中产生,但这些细胞似乎不太可能提供足够的体积用于大规模生产。然而,人类胚胎干细胞(hESC)和潜在的诱导多能干细胞(iPSC)可能为实现这一目标提供了途径。红细胞输注是多能干细胞衍生疗法的一个有吸引力的目标,因为它是一种特征明确的单细胞悬浮液,不含有核细胞,且人类白细胞抗原分子的表达水平较低,但将这种细胞疗法转化为临床应用仍然存在许多挑战。