肿瘤微环境
免疫系统
间质细胞
生物
CD44细胞
细胞生物学
癌症研究
癌症免疫疗法
免疫疗法
调节器
背景(考古学)
免疫学
细胞
基因
遗传学
古生物学
作者
Anamika Bose,Subhasis Barik,Saptak Banerjee,Tithi Ghosh,Atanu Mallick,Suchandra Bhattacharyya Majumdar,Kuntal Kanti Goswami,Avishek Bhuniya,Sayantan Banerjee,Rathindranath Baral,Walter J. Storkus,Partha Dasgupta,Subrata Majumdar
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:2013-06-20
卷期号:191 (2): 971-981
被引量:64
标识
DOI:10.4049/jimmunol.1300280
摘要
Abstract Immune evasion within the tumor microenvironment supports malignant growth and is also a major obstacle for successful immunotherapy. Multiple cellular components and soluble factors coordinate to disrupt protective immune responses. Although stromal cells are well-known for their parenchymal supportive roles in cancer establishment and progression, we demonstrate for the first time, to our knowledge, that tumor-derived vascular pericytes negatively influence CD4+ T cell activation and proliferation, and promote anergy in recall response to Ag by CD4+CD44+ T cells via regulator of G protein signaling 5– and IL-6–dependent pathways. Our data support a new specific role for tumor-derived pericytes in the immune evasion paradigm within the tumor microenvironment and suggest the targeting of these cell populations in the context of successful immunotherapeutics for the treatment of cancer.
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