Michael Maria, Shimoni Avichai, Nagler Arnon
Hematology Division & Bone Marrow Transplantation, Chaim Sheba Medical Center, Sackler Medical School, Tel Aviv University, Tel Aviv 52621, Israel.
Clin Dev Immunol. 2013;2013:608951. doi: 10.1155/2013/608951. Epub 2013 May 8.
Growing evidence suggests that cellular adoptive immunotherapy is becoming an attractive though challenging approach in regulating tumor immunity and alloresponses in clinical transplantation. Naturally arising CD4+CD25+Foxp3+ regulatory T cells (Treg) have emerged as a key component in this regard. Over the last decade, a large body of evidence from preclinical models has demonstrated their crucial role in auto- and tumor immunity and has opened the door to their "first-in-man" clinical application. Initial studies in clinical allogeneic stem cell transplantation are very encouraging and may pave the way for other applications. Further improvements in Treg ex vivo or in vivo expansion technologies will simplify their global clinical application. In this review, we discuss the current knowledge of Treg biology and their potential for cell-based immunotherapy in allogeneic stem cell transplantation.
越来越多的证据表明,细胞过继性免疫疗法正成为一种在临床移植中调节肿瘤免疫和同种异体反应方面颇具吸引力但具有挑战性的方法。天然产生的CD4+CD25+Foxp3+调节性T细胞(Treg)已成为这方面的关键组成部分。在过去十年中,来自临床前模型的大量证据表明它们在自身免疫和肿瘤免疫中起关键作用,并为其“首次人体”临床应用打开了大门。临床同种异体干细胞移植的初步研究非常令人鼓舞,可能为其他应用铺平道路。Treg体外或体内扩增技术的进一步改进将简化其全球临床应用。在本综述中,我们讨论了Treg生物学的当前知识及其在同种异体干细胞移植中基于细胞的免疫治疗的潜力。