Talib Sohel, Millan Maria T, Jorgenson Rebecca L, Shepard Kelly A
California Institute for Regenerative Medicine, San Francisco, California, USA
California Institute for Regenerative Medicine, San Francisco, California, USA.
Stem Cells Transl Med. 2015 Jan;4(1):4-9. doi: 10.5966/sctm.2014-0262. Epub 2014 Dec 3.
The mission of the California Institute for Regenerative Medicine (CIRM) is to accelerate stem cell treatments to patients with unmet medical needs. Immune rejection is one hurdle that stem cell therapies must overcome to achieve a durable and effective therapeutic benefit. In July 2014, CIRM convened a group of clinical investigators developing stem cell therapeutics, immunologists, and transplantation biologists to consider strategies to address this challenge. Workshop participants discussed current approaches for countering immune rejection in the context of organ transplant and cellular therapy and defined the risks, challenges, and opportunities for adapting them to the development of stem cell-based therapeutics. This effort led to the development of a Roadmap to Tolerance for allogeneic stem cell therapy, with four fundamental steps: (a) the need to identify "tolerance-permissive" immune-suppressive regimens to enable the eventual transition from current, drug-based approaches to a newer generation of technologies for inducing tolerance; (b) testing new biologics and small molecules for inducing tolerance in stem cell-based preclinical and clinical studies; (c) stimulation of efforts to develop novel therapeutic approaches to induce central and peripheral tolerance, including manipulation of the thymus, transplantation of purified stem cells, and cell therapy with T-regulatory cells; and (d) development of robust and sensitive immune monitoring technologies for identifying biomarkers of tolerance and rejection after allogeneic stem cell treatments in the clinical setting.
加利福尼亚再生医学研究所(CIRM)的使命是加速向有未满足医疗需求的患者提供干细胞治疗。免疫排斥是干细胞疗法为实现持久有效的治疗效果必须克服的一个障碍。2014年7月,CIRM召集了一群从事干细胞治疗研发的临床研究人员、免疫学家和移植生物学家,共同探讨应对这一挑战的策略。研讨会参与者讨论了在器官移植和细胞治疗背景下对抗免疫排斥的现有方法,并明确了将这些方法应用于基于干细胞的治疗研发中的风险、挑战和机遇。这项工作促成了一份异基因干细胞治疗耐受性路线图的制定,该路线图包含四个基本步骤:(a)需要确定“允许耐受性”的免疫抑制方案,以便最终从当前基于药物的方法过渡到新一代诱导耐受性的技术;(b)在基于干细胞的临床前和临床研究中测试诱导耐受性的新生物制剂和小分子;(c)推动开发诱导中枢和外周耐受性的新型治疗方法,包括操纵胸腺、移植纯化的干细胞以及用调节性T细胞进行细胞治疗;(d)开发强大且灵敏的免疫监测技术,以识别临床环境中异基因干细胞治疗后耐受性和排斥反应的生物标志物。