Hérodin Francis, Mayol Jean-François, Mourcin Frédéric, Drouet Michel
Centre de Recherches du Service de Santé des Armées, PO Box 87, 38702 La Tronche, France.
Folia Histochem Cytobiol. 2005;43(4):223-7.
Radiation-induced (RI) tissue injuries can be caused by radiation therapy, nuclear accidents or radiological terrorism. Notwithstanding the complexity of RI pathophysiology, there are some effective approaches to treatment of both acute and chronic radiation damages. Cytokine therapy is the main strategy capable of preventing or reducing the acute radiation syndrome (ARS), and hematopoietic growth factors (GF) are particularly effective in mitigating bone marrow (BM) aplasia and stimulating hematopoietic recovery. However, first, as a consequence of RI stem and progenitor cell death, use of cytokines should be restricted to a range of intermediate radiation doses (3 to 7 Gy total body irradiation). Second, ARS is a global illness that requires treatment of damages to other tissues (epithelial, endothelial, glial, etc.), which could be achieved using pleiotropic or tissue-specific cytokines. Stem cell therapy (SCT) is a promising approach developed in the laboratory that could expand the ability to treat severe radiation injuries. Allogeneic hematopoietic stem cell transplantation (BM, mobilized peripheral blood and cord blood) transplantation has been used in radiation casualties with variable success due to limiting toxicity related to the degree of graft histocompatibility and combined injuries. Ex vivo expansion should be used to augment cord blood graft size and/or promote very immature stem cells. Autologous SCT might also be applied to radiation casualties from residual hematopoietic stem and progenitor cells (HSPC). Stem cell plasticity of different tissues such as liver or skeletal muscle, may also be used as a source of hematopoietic stem cells. Finally, other types of stem cells such as mesenchymal, endothelial stem cells or other tissue committed stem cells (TCSC), could be used for treating damages to nonhematopoietic organs.
辐射诱导(RI)组织损伤可由放射治疗、核事故或放射性恐怖主义引起。尽管RI病理生理学复杂,但对于急性和慢性辐射损伤都有一些有效的治疗方法。细胞因子疗法是预防或减轻急性放射综合征(ARS)的主要策略,造血生长因子(GF)在减轻骨髓(BM)再生障碍和刺激造血恢复方面特别有效。然而,首先,由于RI干细胞和祖细胞死亡,细胞因子的使用应限于一定范围的中等辐射剂量(全身照射3至7 Gy)。其次,ARS是一种全身性疾病,需要治疗对其他组织(上皮、内皮、神经胶质等)的损伤,这可以使用多效性或组织特异性细胞因子来实现。干细胞疗法(SCT)是实验室开发的一种有前景的方法,可扩展治疗严重辐射损伤的能力。同种异体造血干细胞移植(骨髓、动员外周血和脐带血)已用于辐射伤亡人员,但由于与移植物组织相容性程度和合并损伤相关的毒性限制,成功率不一。体外扩增应用于增加脐带血移植物大小和/或促进非常不成熟的干细胞。自体SCT也可应用于来自残留造血干细胞和祖细胞(HSPC)的辐射伤亡人员。不同组织如肝脏或骨骼肌的干细胞可塑性,也可作为造血干细胞的来源。最后,其他类型的干细胞如间充质干细胞、内皮干细胞或其他组织定向干细胞(TCSC),可用于治疗非造血器官的损伤。