From T cell "exhaustion" to anti-cancer immunity

被引:24
作者
Verdeil, Gregory
Marraco, Silvia A. Fuertes
Murray, Timothy
Speiser, Daniel E. [1 ]
机构
[1] Lausanne Univ Hosp Ctr CHUV, Clin Tumor Biol & Immunotherapy Grp, Ludwig Canc Res Ctr, Route Corniche 9A, CH-1066 Epalinges, Switzerland
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2016年 / 1865卷 / 01期
关键词
T cells; Exhaustion; Tumor microenvironment; Cancer biology; Cancer immunotherapy; Clinical trials; CHRONIC VIRAL-INFECTION; TUMOR-INFILTRATING LYMPHOCYTES; ARYL-HYDROCARBON RECEPTOR; CANCER-IMMUNOTHERAPY; CHECKPOINT BLOCKADE; EFFECTOR FUNCTION; MELANOMA PATIENTS; IN-VIVO; INDOLEAMINE 2,3-DIOXYGENASE; INHIBITORY RECEPTORS;
D O I
10.1016/j.bbcan.2015.06.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The immune system has the potential to protect from malignant diseases for extended periods of time. Unfortunately, spontaneous immune responses are often inefficient. Significant effort is required to develop reliable, broadly applicable immunotherapies for cancer patients. A major innovation was transplantation with hematopoietic stem cells from genetically distinct donors for patients with hematologic malignancies. In this setting, donor T cells induce long-term remission by keeping cancer cells in check through powerful allogeneic graft versus-leukemia effects. More recently, a long awaited breakthrough for patients with solid tissue cancers was achieved, by means of therapeutic blockade of T cell inhibitory receptors. In untreated cancer patients, T cells are dysfunctional and remain in a state of T cell "exhaustion". Nonetheless, they often retain a high potential for successful defense against cancer, indicating that many T cells are not entirely and irreversibly exhausted but can be mobilized to become highly functional. Novel antibody therapies that block inhibitory receptors can lead to strong activation of anti-tumor T cells, mediating clinically significant anti-cancer immunity for many years. Here we review these new treatments and the current knowledge on tumor antigen-specific T cells. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:49 / 57
页数:9
相关论文
共 107 条
  • [51] Mesenchymal Stem Cells Use IDO to Regulate Immunity in Tumor Microenvironment
    Ling, Weifang
    Zhang, Jimin
    Yuan, Zengrong
    Ren, Guangwen
    Zhang, Liying
    Chen, Xiaodong
    Rabson, Arnold B.
    Roberts, Arthur I.
    Wang, Ying
    Shi, Yufang
    [J]. CANCER RESEARCH, 2014, 74 (05) : 1576 - 1587
  • [52] High-throughput epitope discovery reveals frequent recognition of neo-antigens by CD4+ T cells in human melanoma
    Linnemann, Carsten
    van Buuren, Marit M.
    Bies, Laura
    Verdegaal, Els M. E.
    Schotte, Remko
    Calis, Jorg J. A.
    Behjati, Sam
    Velds, Arno
    Hilkmann, Henk
    el Atmioui, Dris
    Visser, Marten
    Stratton, Michael R.
    Haanen, John B. A. G.
    Spits, Hergen
    van der Burg, Sjoerd H.
    Schumacher, Ton N. M.
    [J]. NATURE MEDICINE, 2015, 21 (01) : 81 - 85
  • [53] Transcriptional mechanisms underlying lymphocyte tolerance
    Macián, F
    García-Cózar, F
    Im, SH
    Horton, HF
    Byrne, MC
    Rao, A
    [J]. CELL, 2002, 109 (06) : 719 - 731
  • [54] Long-lasting stem cell-like memory CD8+ T cells with a naive-like profile upon yellow fever vaccination
    Marraco, Silvia A. Fuertes
    Soneson, Charlotte
    Cagnon, Laurene
    Gannon, Philippe O.
    Allard, Mathilde
    Maillard, Samia Abed
    Montandon, Nicole
    Rufer, Nathalie
    Waldvogel, Sophie
    Delorenzi, Mauro
    Speiser, Daniel E.
    [J]. SCIENCE TRANSLATIONAL MEDICINE, 2015, 7 (282)
  • [55] The Transcription Factor NFAT Promotes Exhaustion of Activated CD8+ T Cells
    Martinez, Gustavo J.
    Pereira, Renata M.
    Aijo, Tarmo
    Kim, Edward Y.
    Marangoni, Francesco
    Pipkin, Matthew E.
    Togher, Susan
    Heissmeyer, Vigo
    Zhang, Yi Chen
    Crotty, Shane
    Lamperti, Edward D.
    Ansel, K. Mark
    Mempel, Thorsten R.
    Lahdesmaki, Harri
    Hogan, Patrick G.
    Rao, Anjana
    [J]. IMMUNITY, 2015, 42 (02) : 265 - 278
  • [56] Metabolic control of type 1 regulatory T cell differentiation by AHR and HIF1-α
    Mascanfroni, Ivan D.
    Takenaka, Maisa C.
    Yeste, Ada
    Patel, Bonny
    Wu, Yan
    Kenison, Jessica E.
    Siddiqui, Shafiuddin
    Basso, Alexandre S.
    Otterbein, Leo E.
    Pardoll, Drew M.
    Pan, Fan
    Priel, Avner
    Clish, Clary B.
    Robson, Simon C.
    Quintana, Francisco J.
    [J]. NATURE MEDICINE, 2015, 21 (06) : 638 - 646
  • [57] Naidoo J., 2014, BR CANC
  • [58] Clinical blockade of PD1 and LAG3-potential mechanisms of action
    Nguyen, Linh T.
    Ohashi, Pamela S.
    [J]. NATURE REVIEWS IMMUNOLOGY, 2015, 15 (01) : 45 - 56
  • [59] Molecular Pathways: Coexpression of Immune Checkpoint Molecules: Signaling Pathways and Implications for Cancer Immunotherapy
    Nirschl, Christopher J.
    Drake, Charles G.
    [J]. CLINICAL CANCER RESEARCH, 2013, 19 (18) : 4917 - 4924
  • [60] Cancer-associated fibroblasts and tumor growth - bystanders turning into key players
    Oestman, Arne
    Augsten, Martin
    [J]. CURRENT OPINION IN GENETICS & DEVELOPMENT, 2009, 19 (01) : 67 - 73