Department of Stem Cell Transplantation and Cellular Therapy, University of Texas, M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, Texas 77030, USA.
Best Pract Res Clin Haematol. 2011 Mar;24(1):83-92. doi: 10.1016/j.beha.2010.11.001. Epub 2011 Feb 23.
Umbilical cord blood (CB) is becoming an important source of haematopoietic support for transplant patients lacking human leukocyte antigen matched donors. The ethnic diversity, relative ease of collection, ready availability as cryopreserved units from CB banks, reduced incidence and severity of graft versus host disease and tolerance of higher degrees of HLA disparity between donor and recipient, are positive attributes when compared to bone marrow or cytokine-mobilized peripheral blood. However, CB transplantation is associated with significantly delayed neutrophil and platelet engraftment and an elevated risk of graft failure. These hurdles are thought to be due, at least in part, to low total nucleated cell and CD34(+) cell doses transplanted. Here, current strategies directed at improving TNC and CD34(+) cell doses at transplant are discussed, with particular attention paid to the use of a mesenchymal stem cell (MSC)/CB mononuclear cell ex vivo co-culture expansion system.
脐带血 (CB) 正成为缺乏人类白细胞抗原匹配供体的移植患者造血支持的重要来源。与骨髓或细胞因子动员外周血相比,CB 具有种族多样性、采集相对容易、可从 CB 库中冷冻保存单位随时获得、移植物抗宿主病的发生率和严重程度降低以及对供体和受体之间更高程度的 HLA 差异的耐受性等优点。然而,CB 移植与明显延迟的中性粒细胞和血小板植入以及更高的移植物失败风险相关。这些障碍至少部分归因于移植时总核细胞和 CD34+细胞剂量低。在这里,讨论了目前旨在提高移植时 TNC 和 CD34+细胞剂量的策略,特别关注间充质干细胞 (MSC)/CB 单核细胞体外共培养扩增系统的使用。