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
  • [1] Immunology in the clinic review series; focus on cancer: tumour-associated macrophages: undisputed stars of the inflammatory tumour microenvironment
    Allavena, P.
    Mantovani, A.
    [J]. CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2012, 167 (02) : 195 - 205
  • [2] Transcription factor regulation of CD8+T-cell memory and exhaustion
    Angelosanto, Jill M.
    Wherry, E. John
    [J]. IMMUNOLOGICAL REVIEWS, 2010, 236 : 167 - 175
  • [3] [Anonymous], 2013, BEST PRACT RES CLIN, V26, P293
  • [4] The three main stumbling blocks for anticancer T cells
    Baitsch, Lukas
    Fuertes-Marraco, Silvia A.
    Legat, Amandine
    Meyer, Christiane
    Speiser, Daniel E.
    [J]. TRENDS IN IMMUNOLOGY, 2012, 33 (07) : 364 - 372
  • [5] Exhaustion of tumor-specific CD8+ T cells in metastases from melanoma patients
    Baitsch, Lukas
    Baumgaertner, Petra
    Devevre, Estelle
    Raghav, Sunil K.
    Legat, Amandine
    Barba, Leticia
    Wieckowski, Sebastien
    Bouzourene, Hanifa
    Deplancke, Bart
    Romero, Pedro
    Rufer, Nathalie
    Speiser, Daniel E.
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (06) : 2350 - 2360
  • [6] Checkpoint Blockade Immunotherapy Relies on T-bet but Not Eomes to Induce Effector Function in Tumor-Infiltrating CD8+ T Cells
    Berrien-Elliott, Melissa M.
    Yuan, Jinyun
    Swier, Lauryn E.
    Jackson, Stephanie R.
    Chen, Collin L.
    Donlin, Maureen J.
    Teague, Ryan M.
    [J]. CANCER IMMUNOLOGY RESEARCH, 2015, 3 (02) : 116 - 124
  • [7] Transcriptional insights into the CD8+ T cell response to infection and memory T cell formation
    Best, J. Adam
    Blair, David A.
    Knell, Jamie
    Yang, Edward
    Mayya, Viveka
    Doedens, Andrew
    Dustin, Michael L.
    Goldrath, Ananda W.
    [J]. NATURE IMMUNOLOGY, 2013, 14 (04) : 404 - 412
  • [8] Coregulation of CD8+ T cell exhaustion by multiple inhibitory receptors during chronic viral infection
    Blackburn, Shawn D.
    Shin, Haina
    Haining, W. Nicholas
    Zou, Tao
    Workman, Creg J.
    Polley, Antonio
    Betts, Michael R.
    Freeman, Gordon J.
    Vignali, Dario A. A.
    Wherry, E. John
    [J]. NATURE IMMUNOLOGY, 2009, 10 (01) : 29 - 37
  • [9] T-bet and Eomes Are Differentially Linked to the Exhausted Phenotype of CD8+T Cells in HIV Infection
    Buggert, Marcus
    Tauriainen, Johanna
    Yamamoto, Takuya
    Frederiksen, Juliet
    Ivarsson, Martin A.
    Michaelsson, Jakob
    Lund, Ole
    Hejdeman, Bo
    Jansson, Marianne
    Sonnerborg, Anders
    Koup, Richard A.
    Betts, Michael R.
    Karlsson, Annika C.
    [J]. PLOS PATHOGENS, 2014, 10 (07)
  • [10] CTLA-4 and PD-1 pathway blockade: combinations in the clinic
    Callahan, Margaret K.
    Postow, Michael A.
    Wolchok, Jedd D.
    [J]. FRONTIERS IN ONCOLOGY, 2015, 4