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加鲁尼西替布可导致调节性T细胞功能脆弱,并促进树突状细胞介导的针对实验性淋巴瘤的免疫反应。

Galunisertib Drives Treg Fragility and Promotes Dendritic Cell-Mediated Immunity against Experimental Lymphoma.

作者信息

Hira Sumit Kumar, Rej Abhinandan, Paladhi Ankush, Singh Ranjeet, Saha Jayasree, Mondal Indrani, Bhattacharyya Sankar, Manna Partha Pratim

机构信息

Cellular Immunology Laboratory, Department of Zoology, The University of Burdwan, Bardhaman 713104, India.

Immunobiology Laboratory, Department of Zoology, Banaras Hindu University, Varanasi 221005, India.

出版信息

iScience. 2020 Sep 29;23(10):101623. doi: 10.1016/j.isci.2020.101623. eCollection 2020 Oct 23.

Abstract

Galunisertib (LY2157299) is a selective ATP-mimetic inhibitor of TGF-β receptor-I activation, currently under clinical trial in a variety of cancers. We have tested the combined effects of galunisertib- and interleukin-15-activated dendritic cells in an aggressive and highly metastatic murine lymphoma. Based on the tumor-draining lymph node architecture, and its histology, the combination therapy results in better prognosis, including disappearance of the disease-exacerbating regulatory T cells. Our data suggest that galunisertib significantly enhances the success of immunotherapy with IL-15-activated dendritic cells by limiting the regulatory T cells generation with consequent downregulation of regulatory T cells in the tumor-draining lymph nodes and vascularized organ like spleen. This is also associated with consistent loss p-SMAD2 and downregulation of Neuropilin-1, leading to better prognosis and positive outcome. These results connect the role of combined therapy with the consequent elimination of disease-exacerbating T regulatory cells in a metastatic murine lymphoma.

摘要

加芦米司替(LY2157299)是一种选择性ATP模拟物,可抑制转化生长因子-β受体-I的激活,目前正在多种癌症中进行临床试验。我们已经在侵袭性和高转移性小鼠淋巴瘤中测试了加芦米司替和白细胞介素-15激活的树突状细胞的联合作用。基于引流肿瘤的淋巴结结构及其组织学,联合治疗可带来更好的预后,包括使加剧疾病的调节性T细胞消失。我们的数据表明,加芦米司替通过限制调节性T细胞的生成,从而使引流肿瘤的淋巴结和脾脏等血管化器官中的调节性T细胞下调,显著提高了IL-15激活的树突状细胞免疫治疗的成功率。这也与p-SMAD2的持续缺失和神经纤毛蛋白-1的下调有关,从而带来更好的预后和积极的结果。这些结果将联合治疗的作用与转移性小鼠淋巴瘤中加剧疾病的T调节细胞的消除联系起来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a294/7559877/a9bac05d5c02/fx1.jpg

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