Marcelis Lukas, Tousseyn Thomas
Department of Imaging and Pathology, Translational Cell and Tissue Research Lab, KU Leuven, Herestraat 49 - O&N IV, 3000, Leuven, Belgium.
Department of Pathology, University Hospitals UZ Leuven, 7003 24, Herestraat 49, Leuven, 3000, Belgium.
Cancer Microenviron. 2019 Apr;12(1):3-16. doi: 10.1007/s12307-018-00219-5. Epub 2019 Jan 24.
Post-transplant lymphoproliferative disorders (PTLDs) cover a broad spectrum of lymphoproliferative lesions arising after solid organ or allogeneic hematopoietic stem cell transplantation. The composition and function of the tumor microenvironment (TME), consisting of all non-malignant constituents of a tumor, is greatly impacted in PTLD through a complex interplay between 4 factors: 1) the graft organ causes immune stimulation through chronic antigen presentation; 2) the therapy to prevent organ rejection interferes with the immune system; 3) the oncogenic Epstein-Barr virus (EBV), present in 80% of PTLDs, has a causative role in the oncogenic transformation of lymphocytes and influences immune responses; 4) interaction with the donor-derived immune cells accompanying the graft. These factors make PTLDs an interesting model to look at cancer-microenvironment interactions and current findings can be of interest for other malignancies including solid tumors. Here we will review the current knowledge of the TME composition in PTLD with a focus on the different factors involved in PTLD development.
移植后淋巴细胞增生性疾病(PTLD)涵盖了实体器官或异基因造血干细胞移植后出现的广泛的淋巴细胞增生性病变。肿瘤微环境(TME)由肿瘤的所有非恶性成分组成,其组成和功能在PTLD中受到4个因素之间复杂相互作用的极大影响:1)移植器官通过慢性抗原呈递引起免疫刺激;2)预防器官排斥的治疗会干扰免疫系统;3)80%的PTLD中存在的致癌性爱泼斯坦-巴尔病毒(EBV)在淋巴细胞的致癌转化中起因果作用,并影响免疫反应;4)与移植伴随的供体来源免疫细胞相互作用。这些因素使PTLD成为研究癌症-微环境相互作用的一个有趣模型,目前的研究结果可能对包括实体瘤在内的其他恶性肿瘤具有参考价值。在这里,我们将回顾PTLD中TME组成的当前知识,重点关注PTLD发展中涉及的不同因素。