Enhancement of antibody-dependent cell mediated cytotoxicity: a new era in cancer treatment

被引:43
作者
Rajasekaran, Narendiran [1 ]
Chester, Cariad [1 ]
Yonezawa, Atsushi [1 ,2 ]
Zhao, Xing [1 ,3 ]
Kohrt, Holbrook E. [1 ]
机构
[1] Stanford Univ, Stanford Sch Med, Div Oncol, Stanford, CA 94305 USA
[2] Kyoto Univ Hosp, Dept Clin Pharmacol & Therapeut, Kyoto, Japan
[3] Guiyang Med Univ, Tissue Engn & Stem Cells Res Ctr, Dept Immunol, Guiyang, Guizhou, Peoples R China
关键词
ADCC; NK cell; reovirus; TLR; CD137;
D O I
10.2147/ITT.S61292
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The therapeutic efficacy of some anti-tumor monoclonal antibodies (mAbs) depends on the capacity of the mAb to recognize the tumor-associated antigen and induce cytotoxicity via a network of immune effector cells. This process of antibody-dependent cell-mediated cytotoxicity (ADCC) against tumor cells is triggered by the interaction of the fragment crystallizable (Fc) portion of the mAb with the Fc receptors on effector cells like natural killer cells, macrophages,gamma d T cells, and dendritic cells. By augmenting ADCC, the antitumor activity of mAbs can be significantly increased. Currently, identifying and developing therapeutic agents that enhance ADCC is a growing area of research. Combining existing tumor-targeting mAbs and ADCC-promoting agents that stimulate effector cells will translate to greater clinical responses. In this review, we discuss strategies for enhancing ADCC and emphasize the potential of combination treatments that include US Food and Drug Administration-approved mAbs and immunostimulatory therapeutics.
引用
收藏
页码:91 / 100
页数:10
相关论文
共 109 条
[91]   Herpes simplex virus as an in situ cancer vaccine for the induction of specific anti-tumor immunity [J].
Toda, M ;
Rabkin, SD ;
Kojima, H ;
Martuza, RL .
HUMAN GENE THERAPY, 1999, 10 (03) :385-393
[92]   Natural killer cell cytotoxicity: how do they pull the trigger? [J].
Topham, Nicola J. ;
Hewitt, Eric W. .
IMMUNOLOGY, 2009, 128 (01) :7-15
[93]  
Vacchelli E, 2014, ONCOIMMUNOLOGY, V2
[94]   Trial watch FDA-approved Toll-like receptor agonists for cancer therapy [J].
Vacchelli, Erika ;
Galluzzi, Lorenzo ;
Eggermont, Alexander ;
Fridman, Wolf Herve ;
Galon, Jerome ;
Sautes-Fridman, Catherine ;
Tartour, Eric ;
Zitvogel, Laurence ;
Kroemer, Guido .
ONCOIMMUNOLOGY, 2012, 1 (06) :894-907
[95]  
van Ojik HH, 2003, CANCER RES, V63, P5595
[96]   A phase 1 trial of the anti-inhibitory KIR mAb IPH2101 for AML in complete remission [J].
Vey, Norbert ;
Bourhis, Jean-Henri ;
Boissel, Nicolas ;
Bordessoule, Dominique ;
Prebet, Thomas ;
Charbonnier, Aude ;
Etienne, Anne ;
Andre, Pascale ;
Romagne, Francois ;
Benson, Don ;
Dombret, Herve ;
Olive, Daniel .
BLOOD, 2012, 120 (22) :4317-4323
[97]   A Phase I Study of Intravenous Oncolytic Reovirus Type 3 Dearing in Patients with Advanced Cancer [J].
Vidal, Laura ;
Pandha, Hardev S. ;
Yap, Timothy A. ;
White, Christine L. ;
Twigger, Katie ;
Vile, Richard G. ;
Melcher, Alan ;
Coffey, Matt ;
Harrington, Kevin J. ;
DeBono, Johann S. .
CLINICAL CANCER RESEARCH, 2008, 14 (21) :7127-7137
[98]   KIR: Diverse, rapidly evolving receptors of innate and adaptive immunity [J].
Vilches, C ;
Parham, P .
ANNUAL REVIEW OF IMMUNOLOGY, 2002, 20 :217-251
[99]   Post-translational modifications in the context of therapeutic proteins [J].
Walsh, Gary ;
Jefferis, Roy .
NATURE BIOTECHNOLOGY, 2006, 24 (10) :1241-1252
[100]   Natural killer cells:: from CD3-NKp46+ to post-genomics meta-analyses [J].
Walzer, Thierry ;
Jaeger, Sebastien ;
Chaix, Julie ;
Vivier, Eric .
CURRENT OPINION IN IMMUNOLOGY, 2007, 19 (03) :365-372