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肿瘤免疫、免疫治疗和癌症疫苗的动物模型。

Animal models of tumor immunity, immunotherapy and cancer vaccines.

作者信息

Ostrand-Rosenberg Suzanne

机构信息

Department of Biological Sciences, University of Maryland Baltimore County, 1000 Hilltop Circle Baltimore, MD 21250, USA.

出版信息

Curr Opin Immunol. 2004 Apr;16(2):143-50. doi: 10.1016/j.coi.2004.01.003.

Abstract

Reliable animal models are critical for evaluating immunotherapies and for defining tumor immunology paradigms. Tumor immunologists are moving away from traditional transplantation tumor systems because they do not adequately model human malignancies. Transgenic mouse models in which tumors arise spontaneously have been developed for most cancers. The models use one of three technologies: tissue-specific promoters to drive expression of SV40 large T antigen or tissue-specific oncogenes; deletion of tumor suppressor genes by gene targeting; or, conditional deletion of tumor suppressor genes or activation of oncogenes via Cre-lox technology. Knockin mice expressing human tumor antigens and gene-targeted mice with deletions for immunologically relevant molecules have been integral to advancing knowledge of the tumor-host relationship. Although animal models are becoming more sophisticated, additional improvements are needed so that more realistic models can be developed.

摘要

可靠的动物模型对于评估免疫疗法和界定肿瘤免疫学范式至关重要。肿瘤免疫学家正逐渐摒弃传统的移植瘤系统,因为它们无法充分模拟人类恶性肿瘤。针对大多数癌症,已开发出肿瘤自发产生的转基因小鼠模型。这些模型采用三种技术之一:利用组织特异性启动子驱动SV40大T抗原或组织特异性癌基因的表达;通过基因靶向缺失肿瘤抑制基因;或通过Cre-lox技术条件性缺失肿瘤抑制基因或激活癌基因。表达人类肿瘤抗原的敲入小鼠以及针对免疫相关分子缺失的基因靶向小鼠,对于推进肿瘤-宿主关系的认识不可或缺。尽管动物模型正变得越来越复杂,但仍需要进一步改进,以便开发出更逼真的模型。

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