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从床边到实验室再到农场,然后再回到床边:实验性小鼠模型中的概念性进展如何转化为患者的临床获益。用于黑色素瘤的 T 细胞免疫疗法。

T cell immunotherapy for melanoma from bedside to bench to barn and back: how conceptual advances in experimental mouse models can be translated into clinical benefit for patients.

机构信息

Laboratory of Experimental Dermatology, Department of Dermatology, University Hospital Bonn, Bonn, Germany.

出版信息

Pigment Cell Melanoma Res. 2013 Jul;26(4):441-56. doi: 10.1111/pcmr.12111. Epub 2013 May 15.

Abstract

A solid scientific basis now supports the concept that cytotoxic T lymphocytes can specifically recognize and destroy melanoma cells. Over the last decades, clinicians and basic scientists have joined forces to advance our concepts of melanoma immunobiology. This has catalyzed the rational development of therapeutic approaches to enforce melanoma-specific T cell responses. Preclinical studies in experimental mouse models paved the way for their successful translation into clinical benefit for patients with metastatic melanoma. A more thorough understanding of how melanomas develop resistance to T cell immunotherapy is necessary to extend this success. This requires a continued interdisciplinary effort of melanoma biologists and immunologists that closely connects clinical observations with in vitro investigations and appropriate in vivo mouse models: From bedside to bench to barn and back.

摘要

目前,坚实的科学基础支持细胞毒性 T 淋巴细胞能够特异性识别和破坏黑色素瘤细胞这一概念。在过去的几十年中,临床医生和基础科学家联手推进了我们对黑色素瘤免疫生物学的认识。这促进了治疗方法的合理发展,以增强黑色素瘤特异性 T 细胞反应。实验小鼠模型的临床前研究为其成功转化为转移性黑色素瘤患者的临床获益铺平了道路。为了扩大这一成功,我们有必要更深入地了解黑色素瘤如何对 T 细胞免疫疗法产生耐药性。这需要黑色素瘤生物学家和免疫学家的持续跨学科努力,将临床观察与体外研究和适当的体内小鼠模型紧密联系起来:从床边到实验室,再到农场,然后再回来。

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