Current modalities in cancer immunotherapy: Immunomodulatory antibodies, CARs and vaccines

被引:65
作者
Lohmueller, Jason [1 ]
Finn, Olivera J. [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Immunol, Pittsburgh, PA USA
基金
美国国家卫生研究院;
关键词
Cancer immunotherapy; Cancer vaccine; Immune checkpoint inhibitor; Immunomodulator; Chimeric antigen receptor (CAR); Adoptive cell therapy; RECEPTOR T-CELLS; IMMUNE CHECKPOINT BLOCKADE; CHIMERIC ANTIGEN RECEPTORS; LONG-TERM SURVIVAL; CTLA-4; BLOCKADE; IN-VIVO; ANTITUMOR IMMUNITY; CD28; COSTIMULATION; AGONIST ANTIBODY; DENDRITIC CELLS;
D O I
10.1016/j.pharmthera.2017.03.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Successes of immune checkpoint inhibitors (ICIs) and chimeric antigen receptor (CAR) T cell therapy in curing patients with otherwise lethal cancers have validated immunotherapy as a treatment for cancer and have inspired excitement for its broader potential. Most promising is the ability of each approach to eliminate bulky and advanced-stage cancers and to achieve durable cures. Despite this success, to date only a subset of cancer patients and a limited number of cancer types respond to these therapies. A major goal now is to expand the types of cancer and number of patients who can be successfully treated. To this end a multitude of immunotherapies are being tested clinically in new combinations, and many new immunomodulatory antibodies and CARs are in development. A third major immunotherapeutic approach with renewed interest is cancer vaccines. While over 20 years of therapeutic cancer vaccine trials have met with limited success, these studies have laid the groundwork for the use of therapeutic vaccines in combination with other immunotherapies or alone as prophylactic cancer vaccines. Prophylactic vaccines are now poised to revolutionize cancer prevention as they have done for the prevention of infectious diseases. In this review we examine three major cancer immunotherapy modalities: immunomodulatory antibodies, CART cell therapy and vaccines. For each we describe the current state of the art and outline major challenges and research directions forward. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:31 / 47
页数:17
相关论文
共 210 条
[71]   Anti-CD22-chimeric antigen receptors targeting B-cell precursor acute lymphoblastic leukemia [J].
Haso, Waleed ;
Lee, Daniel W. ;
Shah, Nirali N. ;
Stetler-Stevenson, Maryalice ;
Yuan, Constance M. ;
Pastan, Ira H. ;
Dimitrov, Dimiter S. ;
Morgan, Richard A. ;
FitzGerald, David J. ;
Barrett, David M. ;
Wayne, Alan S. ;
Mackall, Crystal L. ;
Orentas, Rimas J. .
BLOOD, 2013, 121 (07) :1165-1174
[72]   Agonist Anti-Human CD27 Monoclonal Antibody Induces T Cell Activation and Tumor Immunity in Human CD27-Transgenic Mice [J].
He, Li-Zhen ;
Prostak, Naseem ;
Thomas, Lawrence J. ;
Vitale, Laura ;
Weidlick, Jeffrey ;
Crocker, Andrea ;
Pilsmaker, Catherine D. ;
Round, Sarah M. ;
Tutt, Alison ;
Glennie, Martin J. ;
Marsh, Henry ;
Keler, Tibor .
JOURNAL OF IMMUNOLOGY, 2013, 191 (08) :4174-4183
[73]   OX40 engagement and chemotherapy combination provides potent antitumor immunity with concomitant regulatory T cell apoptosis [J].
Hirschhorn-Cymerman, Daniel ;
Rizzuto, Gabrielle A. ;
Merghoub, Taha ;
Cohen, Adam D. ;
Avogadri, Francesca ;
Lesokhin, Alexander M. ;
Weinberg, Andrew D. ;
Wolchok, Jedd D. ;
Houghton, Alan N. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2009, 206 (05) :1103-1116
[74]   Improved Survival with Ipilimumab in Patients with Metastatic Melanoma [J].
Hodi, F. Stephen ;
O'Day, Steven J. ;
McDermott, David F. ;
Weber, Robert W. ;
Sosman, Jeffrey A. ;
Haanen, John B. ;
Gonzalez, Rene ;
Robert, Caroline ;
Schadendorf, Dirk ;
Hassel, Jessica C. ;
Akerley, Wallace ;
van den Eertwegh, Alfons J. M. ;
Lutzky, Jose ;
Lorigan, Paul ;
Vaubel, Julia M. ;
Linette, Gerald P. ;
Hogg, David ;
Ottensmeier, Christian H. ;
Lebbe, Celeste ;
Peschel, Christian ;
Quirt, Ian ;
Clark, Joseph I. ;
Wolchok, Jedd D. ;
Weber, Jeffrey S. ;
Tian, Jason ;
Yellin, Michael J. ;
Nichol, Geoffrey M. ;
Hoos, Axel ;
Urba, Walter J. .
NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (08) :711-723
[75]   Costimulation by chimeric antigen receptors revisited: the T cell antitumor response benefits from combined CD28-OX40 signalling [J].
Hombach, Andreas A. ;
Abken, Hinrich .
INTERNATIONAL JOURNAL OF CANCER, 2011, 129 (12) :2935-2944
[76]   Fc-engineered anti-CD40 antibody enhances multiple effector functions and exhibits potent in vitro and in vivo antitumor activity against hematologic malignancies [J].
Horton, Holly M. ;
Bernett, Matthew J. ;
Peipp, Matthias ;
Pong, Erik ;
Karki, Sher ;
Chu, Seung Y. ;
Richards, John O. ;
Chen, Hsing ;
Repp, Roland ;
Desjarlais, John R. ;
Zhukovsky, Eugene A. .
BLOOD, 2010, 116 (16) :3004-3012
[77]   Role of LAG-3 in regulatory T cells [J].
Huang, CT ;
Workman, CJ ;
Flies, D ;
Pan, XY ;
Marson, AL ;
Zhou, G ;
Hipkiss, EL ;
Ravi, S ;
Kowalski, J ;
Levitsky, HI ;
Powell, JD ;
Pardoll, DM ;
Drake, CG ;
Vignali, DAA .
IMMUNITY, 2004, 21 (04) :503-513
[78]   CEACAM1 regulates TIM-3-mediated tolerance and exhaustion [J].
Huang, Yu-Hwa ;
Zhu, Chen ;
Kondo, Yasuyuki ;
Anderson, Ana C. ;
Gandhi, Amit ;
Russell, Andrew ;
Dougan, Stephanie K. ;
Petersen, Britt-Sabina ;
Melum, Espen ;
Pertel, Thomas ;
Clayton, Kiera L. ;
Raab, Monika ;
Chen, Qiang ;
Beauchemin, Nicole ;
Yazaki, Paul J. ;
Pyzik, Michal ;
Ostrowski, Mario A. ;
Glickman, Jonathan N. ;
Rudd, Christopher E. ;
Ploegh, Hidde L. ;
Franke, Andre ;
Petsko, Gregory A. ;
Kuchroo, Vijay K. ;
Blumberg, Richard S. .
NATURE, 2015, 517 (7534) :386-U566
[79]   The Nonsignaling Extracellular Spacer Domain of Chimeric Antigen Receptors Is Decisive for In Vivo Antitumor Activity [J].
Hudecek, Michael ;
Sommermeyer, Daniel ;
Kosasih, Paula L. ;
Silva-Benedict, Anne ;
Liu, Lingfeng ;
Rader, Christoph ;
Jensen, Michael C. ;
Riddell, Stanley R. .
CANCER IMMUNOLOGY RESEARCH, 2015, 3 (02) :125-135
[80]   Systemic spread is an early step in breast cancer [J].
Huesemann, Yves ;
Geigl, Jochen B. ;
Schubert, Falk ;
Musiani, Piero ;
Meyer, Manfred ;
Burghart, Elke ;
Forni, Guido ;
Eils, Roland ;
Fehm, Tanja ;
Riethmueller, Gert ;
Klein, Christoph A. .
CANCER CELL, 2008, 13 (01) :58-68