Bernaldo-de-Quirós Esther, Pion Marjorie, Martínez-Bonet Marta, Correa-Rocha Rafael
Laboratory of Immune-Regulation, Instituto de Investigación Sanitaria Gregorio Marañón (IiSGM), Madrid, Spain.
Front Pediatr. 2022 May 11;10:862807. doi: 10.3389/fped.2022.862807. eCollection 2022.
Kidney transplantation is the most common solid organ transplant and the preferred treatment for pediatric patients with end-stage renal disease, but it is still not a definitive solution due to immune graft rejection. Regulatory T cells (Treg) and their control over effector T cells is a crucial and intrinsic tolerance mechanism in limiting excessive immune responses. In the case of transplants, Treg are important for the survival of the transplanted organ, and their dysregulation could increase the risk of rejection in transplanted children. Chronic immunosuppression to prevent rejection, for which Treg are especially sensitive, have a detrimental effect on Treg counts, decreasing the Treg/T-effector balance. Cell therapy with Treg cells is a promising approach to restore this imbalance, promoting tolerance and thus increasing graft survival. However, the strategies used to date that employ peripheral blood as a Treg source have shown limited efficacy. Moreover, it is not possible to use this approach in pediatric patients due to the limited volume of blood that can be extracted from children. Here, we outline our innovative strategy that employs the thymus removed during pediatric cardiac surgeries as a source of therapeutic Treg that could make this therapy accessible to transplanted children. The advantageous properties and the massive amount of Treg cells obtained from pediatric thymic tissue (thyTreg) opens a new possibility for Treg therapies to prevent rejection in pediatric kidney transplants. We are recruiting patients in a clinical trial to prevent rejection in heart-transplanted children through the infusion of autologous thyTreg cells (NCT04924491). If its efficacy is confirmed, thyTreg therapy may establish a new paradigm in preventing organ rejection in pediatric transplants, and their allogeneic use would extend its application to other solid organ transplantation.
肾移植是最常见的实体器官移植,也是终末期肾病儿科患者的首选治疗方法,但由于免疫移植排斥反应,它仍不是一个确定性的解决方案。调节性T细胞(Treg)及其对效应T细胞的控制是限制过度免疫反应的关键内在耐受机制。在移植情况下,Treg对移植器官的存活很重要,其失调可能会增加移植儿童排斥反应的风险。用于预防排斥反应的慢性免疫抑制对Treg计数有不利影响,Treg对此尤为敏感,会降低Treg/效应T细胞平衡。用Treg细胞进行细胞治疗是恢复这种失衡、促进耐受从而提高移植物存活率的一种有前景的方法。然而,迄今为止使用外周血作为Treg来源的策略疗效有限。此外,由于儿童可抽取的血量有限,无法在儿科患者中使用这种方法。在此,我们概述了我们创新策略,即利用小儿心脏手术中切除的胸腺作为治疗性Treg的来源,这可以使移植儿童能够接受这种治疗。从儿科胸腺组织(thyTreg)获得的Treg细胞的有利特性和大量细胞为Treg疗法预防小儿肾移植排斥反应开辟了新的可能性。我们正在进行一项临床试验招募患者,通过输注自体thyTreg细胞来预防心脏移植儿童的排斥反应(NCT04924491)。如果其疗效得到证实,thyTreg疗法可能会在预防儿科移植器官排斥反应方面建立新的范例,其异体使用将把它的应用扩展到其他实体器官移植。