Establishment of immune suppression by cancer cells in the tumor microenvironment

被引:0
|
作者
Ishikawa, Hiroyoshi N. [1 ,2 ,3 ]
机构
[1] Natl Canc Ctr, Res Inst, Exploratory Oncol Res & Clin Trial Ctr EPOC, Div Canc Immunol, Tokyo Chiba, Japan
[2] Nagoya Univ, Dept Immunol, Grad Sch Med, Nagoya, Aichi, Japan
[3] Natl Canc Ctr, Res Inst, Div Canc Immunol, EPOC, 5-1-1 Tsukiji,Chuo Ku, Tokyo 1040045, Japan
关键词
cancer immunotherapy; immune checkpoint inhibitors; tumor; microenvironment; immune suppression; immune-genome precision medicine; REGULATORY T-CELLS; ANTITUMOR IMMUNITY; PD-1; BLOCKADE; IMMUNOTHERAPY; SURVEILLANCE; IMMUNOSURVEILLANCE; LYMPHOCYTES; MECHANISMS; EXPRESSION; RESPONSES;
D O I
10.2183/pjab.100.005
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
With the clinical success of immune checkpoint inhibitors (ICIs), cancer immunotherapy has become an important pillar of cancer treatment in various types of cancer. However, more than half of patients fail to respond to ICIs, even in combination, uncovering a limited window of clinical responses. Therefore, it is essential to develop more effective cancer immunotherapies and to define biomarkers for stratifying responders and nonresponders by exploring the immunological landscape in the tumor microenvironment (TME). It has become clear that differences in immune responses in the TME determine the clinical efficacy of cancer immunotherapies. Additionally, gene alterations in cancer cells contribute to the development of the immunological landscape, particularly immune suppression in the TME. Therefore, integrated analyses of immunological and genomic assays are key for understanding diverse immune suppressive mechanisms in the TME. Developing novel strategies to control immune suppression in the TME from the perspective of immunology and the cancer genome is crucial for effective cancer immunotherapy (immune-genome precision medicine).
引用
收藏
页码:114 / 122
页数:9
相关论文
共 50 条
  • [11] MiRNAs as Regulators of Immune Cells in the Tumor Microenvironment of Ovarian Cancer
    Wilczynski, Milosz
    Wilczynski, Jacek
    Nowak, Marek
    CELLS, 2024, 13 (16)
  • [12] Immunomodulatory effects of the tumor microenvironment on immune cells in colon cancer
    Kaumanns, L.
    Adamczyk, A.
    Westendorf, A. M.
    Pastille, E.
    EUROPEAN JOURNAL OF IMMUNOLOGY, 2022, 52 : 293 - 293
  • [13] Regulation of Ovarian Cancer Prognosis by Immune Cells in the Tumor Microenvironment
    Drakes, Maureen L.
    Stiff, Patrick J.
    CANCERS, 2018, 10 (09)
  • [14] Impact of Immune Cells in the Tumor Microenvironment of Prostate Cancer Metastasis
    Messex, Justin K.
    Liou, Geou-Yarh
    LIFE-BASEL, 2023, 13 (02):
  • [15] Myeloid-Derived Suppressor Cells: Critical Cells Driving Immune Suppression in the Tumor Microenvironment
    Parker, Katherine H.
    Beury, Daniel W.
    Ostrand-Rosenberg, Suzanne
    IMMUNOTHERAPY OF CANCER, 2015, 128 : 95 - 139
  • [16] Hypoxia is an essential driver of immune suppression in the tumor microenvironment
    Ai, Midan
    Budhani, Pratha
    Curran, Michael A.
    CANCER IMMUNOLOGY RESEARCH, 2016, 4 (01)
  • [17] Novel mediators of immune suppression within the tumor microenvironment
    Restifo, N. P.
    EUROPEAN JOURNAL OF IMMUNOLOGY, 2016, 46 : 246 - 246
  • [18] Novel "Elements" of Immune Suppression within the Tumor Microenvironment
    Gurusamy, Devikala
    Clever, David
    Eil, Robert
    Restifo, Nicholas P.
    CANCER IMMUNOLOGY RESEARCH, 2017, 5 (06) : 426 - 433
  • [19] Tumor microenvironment in pancreatic cancer (PDAC): interplay between tumor cells, stromal cells and immune cells
    Karamitopoulou, Eva
    Wartenberg, Martin
    Galvan, Jose A.
    Zlobec, Inti
    Lugli, Alessandro
    Perren, Aurel
    CANCER RESEARCH, 2015, 75
  • [20] Innate immune cells in the tumor microenvironment
    Li, Ming O.
    Wolf, Natalie
    Raulet, David H.
    Akkari, Leila
    Pittet, Mikael J.
    Rodriguez, Paulo C.
    Kaplan, Rosandra N.
    Munitz, Ariel
    Zhang, Zemin
    Cheng, Sijin
    Bhardwaj, Nina
    CANCER CELL, 2021, 39 (06) : 725 - 729