Consensus nomenclature for CD8+ T cell phenotypes in cancer

被引:121
作者
Apetoh, Lionel [1 ,2 ,3 ]
Smyth, Mark J. [4 ]
Drake, Charles G. [5 ]
Abastado, Jean-Pierre [6 ]
Apte, Ron N. [7 ]
Ayyoub, Maha [8 ]
Blay, Jean-Yves [9 ,10 ]
Bonneville, Marc [11 ,12 ]
Butterfield, Lisa H. [13 ,14 ,15 ]
Caignard, Anne [16 ]
Castelli, Chiara [17 ]
Cavallo, Federica [18 ]
Celis, Esteban [19 ]
Chen, Lieping [20 ,21 ]
Colombo, Mario P. [22 ]
Comin-Anduix, Begona [23 ]
Coukos, Georges [24 ]
Dhodapkar, Madhav V.
Dranoff, Glenn [25 ,26 ,27 ,28 ]
Frazer, Ian H. [29 ]
Fridman, Wolf-Herve [30 ]
Gabrilovich, Dmitry I. [31 ]
Gilboa, Eli [32 ]
Gnjatic, Sacha [33 ]
Jaeger, Dirk [34 ]
Kalinski, Pawel [35 ]
Kaufman, Howard L. [36 ]
Kiessling, Rolf [37 ]
Kirkwood, John [38 ,39 ]
Knuth, Alexander [40 ]
Liblau, Roland [41 ,42 ,43 ,44 ]
Lotze, Michael T. [45 ]
Lugli, Enrico [46 ]
Marincola, Francesco [47 ]
Melero, Ignacio [48 ]
Melief, Cornelis J. [49 ]
Mempel, Thorsten R. [50 ]
Mittendorf, Elizabeth A. [51 ]
Odun, Kunle [52 ,53 ]
Overwijk, Willem W. [54 ]
Palucka, Anna Karolina [55 ]
Parmiani, Giorgio [56 ]
Ribas, Antoni [23 ]
Romero, Pedro [24 ]
Schreiber, Robert D. [57 ]
Schuler, Gerold [58 ]
Srivastava, Pramod K. [59 ]
Tartour, Eric [60 ,61 ]
Valmori, Danila [8 ,62 ]
van der Burg, Sjoerd H. [63 ]
机构
[1] INSERM, UMR 866, Dijon, France
[2] Ctr Georges Francois Leclerc, Dijon, France
[3] Univ Bourgogne, Dijon, France
[4] QIMR Berghofer Med Res Inst, Herston, Qld, Australia
[5] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
[6] Inst Rech Int Servier, Suresnes, France
[7] Ben Gurion Univ Negev, Fac Hlth Sci, Shraga Segal Dept Microbiol, Immunol & Genet, Beer Sheva, Israel
[8] INSERM, U1102, Equipe Labellisee Ligue Canc, Inst Cancerol Ouest, Nantes St Hreblain, France
[9] Canc Res Ctr Lyon, INSERM UMR 1052, CNRS UMR 5286, Ctr Leon Berard, Lyon, France
[10] Dept Med Oncol, Lyon, France
[11] CRCNA, INSERM U892, CNRS UMR 6299, Nantes, France
[12] Inst Merienx, Lyon, France
[13] Univ Pittsburgh, Inst Canc, Dept Med, Pittsburgh, PA USA
[14] Univ Pittsburgh, Inst Canc, Dept Surg, Pittsburgh, PA USA
[15] Univ Pittsburgh, Inst Canc, Dept Immunol, Pittsburgh, PA USA
[16] INSERM UMR 1116, Paris, France
[17] Fdn IRCCS Ist Nazl Tumori, Dept Expt Oncol & Mol Med, Unit Immunotherapy Human Tumor, Milan, Italy
[18] Univ Turin, Ctr Mol Biotechnol, Dept Mol Biotechnol & Hlth Sci, I-10124 Turin, Italy
[19] Georgia Regents Univ, Ctr Canc, Canc Immunol, Inflammat & Tolerance Program, Augusta, GA USA
[20] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT USA
[21] Yale Univ, Sch Med, Yale Canc Ctr, New Haven, CT USA
[22] Fdn IRCCS Ist Nazl Tumori, Mol Immunol Unit, Dept Expt Oncol & Mol Med, Milan, Italy
[23] Univ Calif Los Angeles, Sch Med, Jonsson Comprehens Canc Ctr Los Angels, Los Angeles, CA 90024 USA
[24] Univ Lausanne, Dept Oncol, Ludwig Ctr Canc Res, CH-1015 Lausanne, Switzerland
[25] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[26] Dana Farber Canc Inst, Canc Vaccine Ctr, Boston, MA 02115 USA
[27] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[28] Harvard Univ, Sch Med, Boston, MA USA
[29] Univ Queensland, Brisbane, Qld 4072, Australia
[30] Univ Paris 05, Cordeliers Res Ctr, Paris, France
[31] Wistar Inst Anat & Biol, Translat Tumor Immunol, Philadelphia, PA 19104 USA
[32] Univ Miami, Miller Sch Med, Dodson Interdisciplinary Immunotherapy Inst, Dept Microbiol & Immunol,Sylvester Comprehens Can, Miami, FL USA
[33] Icahn Sch Med Mt Sinai, Tisch Canc Inst, New York, NY 10029 USA
[34] Univ Heidelberg Hosp, Internal Med 4, Natl Ctr Tumor Dis, Dept Med Oncol, Heidelberg, Germany
[35] Univ Pittsburgh, Dept Surg, Pittsburgh, PA USA
[36] Rutgers Canc Inst New Jersey, New Brunswick, NJ USA
[37] Karolinska Inst, Dept Oncol Pathol, Stockholm, Sweden
[38] Univ Pittsburgh, Dept Med, Sch Med, Div Hematol Oncol, Pittsburgh, PA USA
[39] Univ Pittsburgh, Inst Canc, Melanoma & Skin Canc Program, Pittsburgh, PA USA
[40] Natl Ctr Canc Care & Res, Doha, Qatar
[41] INSERM UMR 1043, Toulouse, France
[42] CNRS, U5282, Toulouse, France
[43] Univ Toulouse, UPS, Ctr Physiopathol Toulouse Purpan, Toulouse, France
[44] CHU Toulouse Purpan, Toulouse, France
[45] Univ Pittsburgh, Sch Hlth Sci, Hillman Canc Ctr, Pittsburgh, PA USA
[46] Humanitas Clin & Res Ctr, Unit Clin & Expt Immunol, Rozzano, Italy
[47] Sidra Med & Res Ctr, Res Branch, Doha, Qatar
[48] Univ Navarra, Div Oncol, Ctr Appl Med Res & Clin, E-31080 Pamplona, Spain
[49] Leiden Univ, ISA Pharmaceut, NL-2300 RA Leiden, Netherlands
[50] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Ctr Immunol & Inflammatory Dis, Boston, MA USA
基金
英国医学研究理事会;
关键词
anergy; anticancer immunity; CD8(+) T cells; cytotoxicity; exhaustion; effector; IFN gamma; senescence; stemness; CHRONIC VIRAL-INFECTION; ANTIGEN-LOSS VARIANTS; TUMOR-SPECIFIC CTL; ANTITUMOR IMMUNITY; REPLICATIVE SENESCENCE; MELANOMA PATIENTS; INTERFERON-GAMMA; DENDRITIC CELLS; IN-VITRO; INHIBITORY RECEPTORS;
D O I
10.1080/2162402X.2014.998538
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Whereas preclinical investigations and clinical studies have established that CD8+ T cells can profoundly affect cancer progression, the underlying mechanisms are still elusive. Challenging the prevalent view that the beneficial effect of CD8+ T cells in cancer is solely attributable to their cytotoxic activity, several reports have indicated that the ability of CD8+T cells to promote tumor regression is dependent on their cytokine secretion profile and their ability to self-renew. Evidence has also shown that the tumor microenvironment can disarm CD8+ T cell immunity, leading to the emergence of dysfunctional CD8+ T cells. The existence of different types of CD8+ T cells in cancer calls for a more precise definition of the CD8+ T cell immune phenotypes in cancer and the abandonment of the generic terms “pro-tumor” and “antitumor.” Based on recent studies investigating the functions of CD8+ T cells in cancer, we here propose some guidelines to precisely define the functional states of CD8+T cells in cancer. © 2015 Taylor & Francis Group, LLC.
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页数:10
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