Unit of Clinical and Experimental Immunology, Humanitas Clinical and Research Center, Milan, Italy.
Department of Medical Biotechnologies and Translational Medicine (BioMeTra), University of Milan, Milan, Italy.
Front Immunol. 2019 Nov 28;10:2794. doi: 10.3389/fimmu.2019.02794. eCollection 2019.
In the context of allogeneic transplant platforms, human leukocyte antigen (HLA)-haploidentical hematopoietic stem cell transplantation (haplo-HSCT) represents one of the latest and most promising curative strategies for patients affected by high-risk hematologic malignancies. Indeed, this platform ensures a suitable stem cell source immediately available for virtually any patents in need. Moreover, the establishment in recipients of a state of immunologic tolerance toward grafted hematopoietic stem cells (HSCs) remarkably improves the clinical outcome of this transplant procedure in terms of overall and disease free survival. However, the HLA-mismatch between donors and recipients has not been yet fully exploited in order to optimize the Graft vs. Leukemia effect. Furthermore, the efficacy of haplo-HSCT is currently hampered by several life-threatening side effects including the onset of Graft vs. Host Disease (GvHD) and the occurrence of opportunistic viral infections. In this context, the quality and the kinetic of the immune cell reconstitution (IR) certainly play a major role and several experimental efforts have been greatly endorsed to better understand and accelerate the post-transplant recovery of a fully competent immune system in haplo-HSCT. In particular, the IR of innate immune system is receiving a growing interest, as it recovers much earlier than T and B cells and it is able to rapidly exert protective effects against both tumor relapses, GvHD and the onset of life-threatening opportunistic infections. Herein, we review our current knowledge in regard to the kinetic and clinical impact of Natural Killer (NK), γδ and Innate lymphoid cells (ILCs) IRs in both allogeneic and haplo-HSCT. The present paper also provides an overview of those new therapeutic strategies currently being implemented to boost the alloreactivity of the above-mentioned innate immune effectors in order to ameliorate the prognosis of patients affected by hematologic malignancies and undergone transplant procedures.
在异基因移植平台中,人类白细胞抗原(HLA)-单倍体造血干细胞移植(haplo-HSCT)是治疗高危血液恶性肿瘤患者的最新且最有前途的治愈策略之一。实际上,该平台确保了几乎任何有需要的患者都能立即获得合适的干细胞来源。此外,受者中对移植造血干细胞(HSCs)产生免疫耐受状态可显著改善该移植程序在总生存率和无病生存率方面的临床结果。然而,供者和受者之间的 HLA 不匹配尚未得到充分利用,以优化移植物抗白血病效应。此外,haplo-HSCT 的疗效目前受到包括移植物抗宿主病(GvHD)和机会性病毒感染在内的几种危及生命的副作用的限制。在这种情况下,免疫细胞重建(IR)的质量和动力学肯定起着重要作用,已经进行了大量的实验努力来更好地理解和加速 haplo-HSCT 中完全功能免疫系统的移植后恢复。特别是,固有免疫系统的 IR 受到越来越多的关注,因为它比 T 和 B 细胞恢复得更早,并且能够迅速对肿瘤复发、GvHD 和危及生命的机会性感染的发生产生保护作用。在此,我们回顾了我们在 NK、γδ 和固有淋巴样细胞(ILCs)IR 的动力学和临床影响方面的当前知识,这些细胞在异基因和 haplo-HSCT 中都有涉及。本文还概述了目前正在实施的那些新的治疗策略,以增强上述固有免疫效应物的同种异体反应性,从而改善接受血液恶性肿瘤和移植程序的患者的预后。