Immunotherapy comes of age: Immune aging & checkpoint inhibitors

被引:112
作者
Elias, Rawad [1 ,2 ]
Karantanos, Theodoros [3 ]
Sira, Elizabeth [4 ]
Hartshorn, Kevan L. [1 ]
机构
[1] Boston Univ, Sch Med, Hematol Oncol Sect, Boston, MA 02118 USA
[2] Boston Univ, Sch Med, Sect Geriatr, Boston, MA 02118 USA
[3] Boston Univ, Sch Med, Dept Internal Med, Boston, MA 02118 USA
[4] New York Med Coll, Grad Sch Basic Med Sci, Valhalla, NY 10595 USA
关键词
Immune checkpoint inhibitors; Immunotherapy; Immunosenescence; Aging; Immune aging; Older adults; REGULATORY T-CELLS; PLASMACYTOID DENDRITIC CELLS; NATURAL-KILLER-CELL; SUPPRESSOR-CELLS; B-CELL; ANTITUMOR IMMUNITY; CANCER-PATIENTS; LUNG-CANCER; ANTI-PD-1; ANTIBODY; CLONAL EXPANSION;
D O I
10.1016/j.jgo.2017.02.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immune checkpoint inhibitors (ICIs) are based on the understanding that there are multilayered checks and balances which can be manipulated to unleash already existing, but paralyzed, immune responses to cancer. These agents are safer and more efficacious than classic cytotoxic drugs making them a very attractive therapeutic option, especially in older adults. Current available data do not suggest significant age-associated differences in the clinical profile of ICIs. It must be noted, however, that there is still relatively little information on the use of ICIs in adults over 75 years of age and aging is associated with a decline in the immune system or "immunosenescence" which theoretically can reduce the efficacy of these immune based therapies. In this paper, we review the mechanism of action of ICIs, current clinical data on their use in older adults, and age associated immune changes that might have a direct impact on their activity in this population. We chose to focus on mainly adaptive cellular immunity, and especially on components of the immune system that are implicated directly in the immune checkpoint process. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:229 / 235
页数:7
相关论文
共 126 条
[1]   Dendritic cells in human aging [J].
Agrawal, Anshu ;
Agrawal, Sudhanshu ;
Gupta, Sudhir .
EXPERIMENTAL GERONTOLOGY, 2007, 42 (05) :421-426
[2]   Lymphostromal interactions in thymic development and function [J].
Anderson, G ;
Jenkinson, EJ .
NATURE REVIEWS IMMUNOLOGY, 2001, 1 (01) :31-40
[3]  
[Anonymous], CLIN CANC RES
[4]   PD-1 Blockade with Nivolumab in Relapsed or Refractory Hodgkin's Lymphoma [J].
Ansell, Stephen M. ;
Lesokhin, Alexander M. ;
Borrello, Ivan ;
Halwani, Ahmad ;
Scott, Emma C. ;
Gutierrez, Martin ;
Schuster, Stephen J. ;
Millenson, Michael M. ;
Cattry, Deepika ;
Freeman, Gordon J. ;
Rodig, Scott J. ;
Chapuy, Bjoern ;
Ligon, Azra H. ;
Zhu, Lili ;
Grosso, Joseph F. ;
Kim, Su Young ;
Timmerman, John M. ;
Shipp, Margaret A. ;
Armand, Philippe .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 372 (04) :311-319
[5]   Restoring function in exhausted CD8 T cells during chronic viral infection [J].
Barber, DL ;
Wherry, EJ ;
Masopust, D ;
Zhu, BG ;
Allison, JP ;
Sharpe, AH ;
Freeman, GJ ;
Ahmed, R .
NATURE, 2006, 439 (7077) :682-687
[6]   Quantification of regulatory T cells enables the identification of high-risk breast cancer patients and those at risk of late relapse [J].
Bates, Gaynor J. ;
Fox, Stephen B. ;
Han, Cheng ;
Leek, Russell D. ;
Garcia, Jose F. ;
Harris, Adrian L. ;
Banham, Alison H. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (34) :5373-5380
[7]   The PD-1/PD-L1 axis modulates the natural killer cell versus multiple myeloma effect: a therapeutic target for CT-011, a novel monoclonal anti-PD-1 antibody [J].
Benson, Don M., Jr. ;
Bakan, Courtney E. ;
Mishra, Anjali ;
Hofmeister, Craig C. ;
Efebera, Yvonne ;
Becknell, Brian ;
Baiocchi, Robert A. ;
Zhang, Jianying ;
Yu, Jianhua ;
Smith, Megan K. ;
Greenfield, Carli N. ;
Porcu, Pierluigi ;
Devine, Steven M. ;
Rotem-Yehudar, Rinat ;
Lozanski, Gerard ;
Byrd, John C. ;
Caligiuri, Michael A. .
BLOOD, 2010, 116 (13) :2286-2294
[8]   Can exercise-related improvements in immunity influence cancer prevention and prognosis in the elderly? [J].
Bigley, Austin B. ;
Spielmann, Guillaume ;
LaVoy, Emily C. P. ;
Simpson, Richard J. .
MATURITAS, 2013, 76 (01) :51-56
[9]   PD-L1/B7H-1 inhibits the effector phase of tumor rejection by T cell receptor (TCR) transgenic CD8+ T cells [J].
Blank, C ;
Brown, I ;
Peterson, AC ;
Spiotto, M ;
Iwai, Y ;
Honjo, T ;
Gajewski, TF .
CANCER RESEARCH, 2004, 64 (03) :1140-1145
[10]   Expression of CD57 defines replicative senescence and antigen-induced apoptotic death of CD8+ T cells [J].
Brenchley, JM ;
Karandikar, NJ ;
Betts, MR ;
Ambrozak, DR ;
Hill, BJ ;
Crotty, LE ;
Casazza, JP ;
Kuruppu, J ;
Migueles, SA ;
Connors, M ;
Roederer, M ;
Douek, DC ;
Koup, RA .
BLOOD, 2003, 101 (07) :2711-2720