Adoptive immunotherapy of cancer using CD4+ T cells

被引:227
作者
Muranski, Pawel [1 ]
Restifo, Nicholas P. [1 ]
机构
[1] NCI, NIH, Bethesda, MD 20892 USA
关键词
ROR-GAMMA-T; HELPER-CELLS; IFN-GAMMA; METASTATIC MELANOMA; TUMOR-ERADICATION; ORPHAN RECEPTOR; CUTTING EDGE; TH17; CELLS; IN-VIVO; ANTIGEN;
D O I
10.1016/j.coi.2009.02.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
CD4(+) T cells are central to the function of the immune system but their role in tumor immunity remains underappreciated. It is becoming clear that there is an enormous diversity of CD4(+) T cell polarization patterns including Th1, Th2, Th17, and regulatory T cells (Tregs). These functionally divergent T cell subsets can have opposing effects - they can trigger tumor rejection or inhibit treatment after adoptive cell transfer. Some polarized CD4(+) cells have plasticity, and their phenotypes and functions can evolve in vivo. Recent advances in understanding of polarization and differentiation of lymphocytes, as well as some intriguing developments in the clinic, indicate that the use of CD4(+) T cell subsets in the immunotherapy of cancer has unrealized potential.
引用
收藏
页码:200 / 208
页数:9
相关论文
共 91 条
[1]
CD8+T cell immunity against a tumor/self-antigen is augmented by CD4+ T helper cells and hindered by naturally occurring T regulatory cells [J].
Antony, PA ;
Piccirillo, CA ;
Akpinarli, A ;
Finkelstein, SE ;
Speiss, PJ ;
Surman, DR ;
Palmer, DC ;
Chan, CC ;
Klebanoff, CA ;
Overwijk, WW ;
Rosenberg, SA ;
Restifo, NP .
JOURNAL OF IMMUNOLOGY, 2005, 174 (05) :2591-2601
[2]
TH-17 cells in the circle of immunity and autoimmunity [J].
Bettelli, Estelle ;
Oukka, Mohamed ;
Kuchroo, Vijay K. .
NATURE IMMUNOLOGY, 2007, 8 (04) :345-350
[3]
Helping the CD8+ T-cell response [J].
Bevan, MJ .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (08) :595-602
[4]
The role of IFN-γ in tumor transplantation immunity and inhibition of chemical carcinogenesis [J].
Blankenstein, T ;
Qin, ZH .
CURRENT OPINION IN IMMUNOLOGY, 2003, 15 (02) :148-154
[5]
Complete responses of relapsed lymphoma following genetic modification of tumor-antigen presenting cells and T-lymphocyte transfer [J].
Bollard, Catherine M. ;
Gottschalk, Stephen ;
Leen, Ann M. ;
Weiss, Heidi ;
Straathof, Karin C. ;
Carrum, George ;
Khalil, Mariam ;
Wu, Meng-fen ;
Huls, M. Helen ;
Chang, Chung-Che ;
Gresik, M. Victoria ;
Gee, Adrian P. ;
Brenner, Malcolm K. ;
Rooney, Cliona M. ;
Heslop, Helen E. .
BLOOD, 2007, 110 (08) :2838-2845
[6]
Adoptive transfer of allogeneic tumor-specific T cells mediates effective regression of large tumors across major histocompatibility barriers [J].
Boni, Andrea ;
Muranski, Pawel ;
Cassard, Lydie ;
Wrzesinski, Claudia ;
Paulos, Chrystal M. ;
Palmer, Douglas C. ;
Gattinoni, Luca ;
Hinrichs, Christian S. ;
Chan, Chi-Chao ;
Rosenberg, Steven A. ;
Restifo, Nicholas P. .
BLOOD, 2008, 112 (12) :4746-4754
[7]
Bourgeois C, 2002, EUR J IMMUNOL, V32, P2199, DOI 10.1002/1521-4141(200208)32:8<2199::AID-IMMU2199>3.0.CO
[8]
2-L
[9]
Primary antitumor immune response mediated by CD4+ T cells [J].
Corthay, A ;
Skovseth, DK ;
Lundin, KU ;
Rosjo, E ;
Omholt, H ;
Hofgaard, PO ;
Haraldsen, G ;
Bogen, B .
IMMUNITY, 2005, 22 (03) :371-383
[10]
Helping and harming have something in common [J].
Debes, Gudrun F. ;
Reiner, Steven L. .
NATURE IMMUNOLOGY, 2009, 10 (02) :138-140