Burt Richard K, Slavin Shimon, Burns William H, Marmont Alberto M
Division of Immune Therapy and Autoimmune Disease, Northwestern University Medical Center, 320 E. Superior, Searle Bldg. Rm 3-489, Chicago, IL 60611, USA.
Blood. 2002 Feb 1;99(3):768-84. doi: 10.1182/blood.v99.3.768.
Hematopoietic stem cells (HSCs) are the earliest cells of the immune system, giving rise to B and T lymphocytes, monocytes, tissue macrophages, and dendritic cells. In animal models, adoptive transfer of HSCs, depending on circumstances, may cause, prevent, or cure autoimmune diseases. Clinical trials have reported early remission of otherwise refractory autoimmune disorders after either autologous or allogeneic hematopoietic stem cell transplantation (HSCT). By percentage of transplantations performed, autoimmune diseases are the most rapidly expanding indication for stem cell transplantation. Although numerous editorials or commentaries have been previously published, no prior review has focused on the immunology of transplantation tolerance or development of phase 3 autoimmune HSCT trials. Results from current trials suggest that mobilization of HSCs, conditioning regimen, eligibility and exclusion criteria, toxicity, outcome, source of stem cells, and posttransplantation follow-up need to be disease specific. HSCT-induced remission of an autoimmune disease allows for a prospective analysis of events involved in immune tolerance not available in cross-sectional studies.
造血干细胞(HSCs)是免疫系统中最早的细胞,可分化产生B淋巴细胞、T淋巴细胞、单核细胞、组织巨噬细胞和树突状细胞。在动物模型中,根据具体情况,造血干细胞的过继转移可能引发、预防或治愈自身免疫性疾病。临床试验报告称,自体或异基因造血干细胞移植(HSCT)后,原本难治的自身免疫性疾病可实现早期缓解。按移植手术的占比计算,自身免疫性疾病是干细胞移植中增长最为迅速的适应症。尽管此前已发表了众多社论或评论,但尚无先前的综述聚焦于移植耐受的免疫学或3期自身免疫性HSCT试验的开展情况。当前试验的结果表明,造血干细胞的动员、预处理方案、入选和排除标准、毒性、疗效、干细胞来源以及移植后的随访需要因病而异。HSCT诱导的自身免疫性疾病缓解使得对免疫耐受相关事件进行前瞻性分析成为可能,而这在横断面研究中是无法实现的。