The use of congenitally immunodeficient mice to study human tumor metastases and immunotherapy.

J J Mulé, D L Jicha, S A Rosenberg
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引用次数: 16

Abstract

Congenitally immunodeficient strains of mice have proven valuable in the development of relevant models to study human tumor biology, metastases, and immunotherapy. Local invasion and extensive multiorgan metastases in athymic mice have been obtained following orthotopic implantation or onplantation of histologically intact fragments of human tumors. In C.B-17 severe combined immunodeficient (SCID) mice or in triple immunodeficient, beige/nude/xid (BNX) mice, the development and spread of inoculated human leukemia/lymphoma and/or melanoma have mimicked, in some cases, those observed in patients. Reports of reconstitution of SCID and BNX mice with human myeloid or lymphoid cells have suggested that these models might be useful for the study of human immune responses to autologous tumors in vivo. The severe immunocompromised status of these mice have also led to evaluations of the therapeutic efficacy of adoptively transferred, tumor-reactive human T cells. In this report, we review the pertinent information currently available on the use of congenitally immunodeficient mice in studies of human cancer biology and treatment.

利用先天性免疫缺陷小鼠研究人类肿瘤转移和免疫治疗。
先天免疫缺陷小鼠在研究人类肿瘤生物学、转移和免疫治疗的相关模型中具有重要价值。组织学完整的人类肿瘤碎片原位植入或外植后,胸腺小鼠可发生局部侵袭和广泛的多器官转移。在C.B-17严重联合免疫缺陷(SCID)小鼠或三重免疫缺陷(beige/nude/xid)小鼠中,接种的人类白血病/淋巴瘤和/或黑色素瘤的发展和传播在某些情况下模仿了在患者中观察到的情况。用人髓细胞或淋巴细胞重建SCID和BNX小鼠的报道表明,这些模型可能有助于研究人体内对自体肿瘤的免疫反应。这些小鼠的严重免疫功能低下状态也导致了过继转移的肿瘤反应性人类T细胞治疗效果的评估。在这篇报告中,我们回顾了目前在人类癌症生物学和治疗研究中使用先天性免疫缺陷小鼠的相关信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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