Department of Medical Microbiology and Immunology, University of Wisconsin School of Medicine and Public Health, Madison, WI, United States.
Front Immunol. 2018 Jan 26;9:54. doi: 10.3389/fimmu.2018.00054. eCollection 2018.
Mice engrafted with human immune cells offer powerful model systems to investigate molecular and cellular processes of tumorigenesis, as well as to test therapeutic approaches to treat the resulting cancer. The use of umbilical cord blood mononuclear cells as a source of human immune cells for engraftment is technically straightforward, and provides T lymphocytes and autologous antigen-presenting cells (including B cells, monocytes, and DCs) that bear cognate antigen presenting molecules. By using a human-specific oncogenic virus, such as Epstein-Barr virus, neoplastic transformation of the human B cells can be induced in a manner that models progressive stages of tumorigenesis from nascent neoplasia to the establishment of vascularized tumor masses with an immunosuppressive environment. Moreover, since tumorigenesis occurs in the presence of autologous T cells, this type of system can be used to investigate how T cells become suppressed during tumorigenesis, and how immunotherapies counteract immunosuppression. This minireview will provide a brief overview of the use of human umbilical cord blood transplanted into immunodeficient murine hosts to model antitumor responses.
用人脐带血中的单核细胞作为移植的人类免疫细胞来源,技术上较为简单,并且可以提供 T 淋巴细胞和自体抗原呈递细胞(包括 B 细胞、单核细胞和 DC),这些细胞携带同源抗原呈递分子。通过使用人类特异性致癌病毒,如 Epstein-Barr 病毒,可以诱导人类 B 细胞的肿瘤转化,以模拟肿瘤发生的渐进阶段,从新生肿瘤到建立具有免疫抑制环境的血管化肿瘤块。此外,由于肿瘤发生在自体 T 细胞存在的情况下,这种类型的系统可用于研究 T 细胞在肿瘤发生过程中如何受到抑制,以及免疫疗法如何对抗免疫抑制。这篇简评将简要介绍用人脐带血移植到免疫缺陷的小鼠宿主中,以模拟抗肿瘤反应的应用。