Development and Characterization of Monoclonal Antibodies Specific for Mouse and Human Fcγ Receptors

被引:37
作者
Tutt, Alison L. [1 ]
James, Sonya [1 ]
Laversin, Stephanie A. [1 ]
Tipton, Thomas R. W. [1 ]
Ashton-Key, Margaret [1 ]
French, Ruth R. [1 ]
Hussain, Khiyam [1 ]
Vaughan, Andrew T. [1 ]
Dou, Lang [1 ]
Earley, Alexander [1 ]
Dahal, Lekh N. [1 ]
Lu, Chen [1 ]
Dunscombe, Melanie [1 ]
Chan, H. T. Claude [1 ]
Penfold, Christine A. [1 ]
Kim, Jinny H. [1 ]
Potter, Elizabeth A. [1 ]
Mockridge, C. Ian [1 ]
Roghanian, Ali [1 ]
Oldham, Robert J. [1 ]
Cox, Kerry L. [1 ]
Lim, Sean H. [1 ]
Teige, Ingrid [2 ]
Frendeus, Bjorn [2 ]
Glennie, Martin J. [1 ]
Beers, Stephen A. [1 ]
Cragg, Mark S. [1 ]
机构
[1] Univ Southampton, Southampton Gen Hosp, Fac Med, Canc Sci Unit,Antibody & Vaccine Grp, Southampton SO16 6YD, Hants, England
[2] BioInvent Int, S-22362 Lund, Sweden
关键词
COPY-NUMBER VARIATION; ANTITUMOR ACTIVITIES; ENDOTHELIAL-CELLS; RIIB CD32B; GENE; IGG; EXPRESSION; THERAPY; INTERNALIZATION; AFFINITY;
D O I
10.4049/jimmunol.1402988
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
Fc gamma Rs are key regulators of the immune response, capable of binding to the Fc portion of IgG Abs and manipulating the behavior of numerous cell types. Through a variety of receptors, isoforms, and cellular expression patterns, they are able to fine-tune and direct appropriate responses. Furthermore, they are key determinants of mAb immunotherapy, with mAb isotype and Fc gamma R interaction governing therapeutic efficacy. Critical to understanding the biology of this complex family of receptors are reagents that are robust and highly specific for each receptor. In this study, we describe the development and characterization of mAb panels specific for both mouse and human Fc gamma R for use in flow cytometry, immunofluorescence, and immunocytochemistry. We highlight key differences in expression between the two species and also patterns of expression that will likely impact on immunotherapeutic efficacy and translation of therapeutic agents from mouse to clinic.
引用
收藏
页码:5503 / 5516
页数:14
相关论文
共 57 条
[1]
Affinity and kinetics of the interaction between soluble trimeric OX40 ligand, a member of the tumor necrosis factor superfamily, and its receptor OX40 on activated T cells [J].
AlShamkhani, A ;
Mallett, S ;
Brown, MH ;
James, W ;
Barclay, AN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (08) :5275-5282
[2]
Cell Contact-Dependent Priming and Fc Interaction with CD32+ Immune Cells Contribute to the TGN1412-Triggered Cytokine Response [J].
Bartholomaeus, Patrick ;
Semmler, Linda Y. ;
Bukur, Thomas ;
Boisguerin, Valesca ;
Roemer, Paula S. ;
Tabares, Paula ;
Chuvpilo, Sergey ;
Tyrsin, Dmitry Y. ;
Matskevich, Alexey ;
Hengel, Hartmut ;
Castle, John ;
Unig, Thomas H. ;
Kalinke, Ulrich .
JOURNAL OF IMMUNOLOGY, 2014, 192 (05) :2091-2098
[3]
Type II (tositumomab) anti-CD20 monoclonal antibody out performs type I (rituximab-like) reagents in B-cell depletion regardless of complement activation [J].
Beers, Stephen A. ;
Chan, Claude H. T. ;
James, Sonya ;
French, Ruth R. ;
Attfield, Kathrine E. ;
Brennan, Claire M. ;
Ahuja, Anupama ;
Shlomchik, Mark J. ;
Cragg, Mark S. ;
Glennie, Martin J. .
BLOOD, 2008, 112 (10) :4170-4177
[4]
CD20 as a Target for Therapeutic Type I and II Monoclonal Antibodies [J].
Beers, Stephen A. ;
Chan, Claude H. T. ;
French, Ruth R. ;
Cragg, Mark S. ;
Glennie, Martin J. .
SEMINARS IN HEMATOLOGY, 2010, 47 (02) :107-114
[5]
Flow cytometric assay for detennination of FcγRIIIA-158 V/F polymorphism [J].
Böttcher, S ;
Ritgen, M ;
Brüggemann, M ;
Raff, T ;
Lüschen, S ;
Humpe, A ;
Kneba, M ;
Pott, C .
JOURNAL OF IMMUNOLOGICAL METHODS, 2005, 306 (1-2) :128-136
[6]
Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpura [J].
Breunis, Willernijn B. ;
van Mirre, Edwin ;
Bruin, Marrie ;
Geissler, Judy ;
de Boer, Martin ;
Peters, Marjolein ;
Roos, Dirk ;
de Haas, Masja ;
Koene, Harry R. ;
Kuijpers, Taco W. .
BLOOD, 2008, 111 (03) :1029-1038
[7]
Activating Fc γ receptors contribute to the antitumor activities of immunoregulatory receptor-targeting antibodies [J].
Bulliard, Yannick ;
Jolicoeur, Rose ;
Windman, Maurice ;
Rue, Sarah M. ;
Ettenberg, Seth ;
Knee, Deborah A. ;
Wilson, Nicholas S. ;
Dranoff, Glenn ;
Brogdon, Jennifer L. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2013, 210 (09) :1685-1693
[8]
Technical pitfalls potentially affecting diagnoses in immunohistochemistry [J].
Bussolati, G. ;
Leonardo, E. .
JOURNAL OF CLINICAL PATHOLOGY, 2008, 61 (11) :1184-1192
[9]
Selective expression of inhibitory Fcγ receptor by metastatic melanoma impairs tumor susceptibility to IgG-dependent cellular response [J].
Cassard, Lvdie ;
Cohen-Solal, Joel F. G. ;
Fournier, Emilie M. ;
Camilleri-Broet, Sophie ;
Spatz, Alain ;
Chouaib, Salem ;
Badoual, Cecile ;
Varin, Audrey ;
Fisson, Sylvain ;
Duvillard, Pierre ;
Boix, Charlotte ;
Loncar, Shannon M. ;
Sastre-Garau, Xavier ;
Houghton, Alan N. ;
Avrill, Marie-Francoise ;
Gresser, Ion ;
Fridman, Wolf H. ;
Sautes-Fridman, Catherine .
INTERNATIONAL JOURNAL OF CANCER, 2008, 123 (12) :2832-2839
[10]
Metastatic Melanomas Express Inhibitory Low Affinity Fc Gamma Receptor and Escape Humoral Immunity [J].
Cohen-Solal, Joel F. G. ;
Cassard, Lydie ;
Fournier, Emilie M. ;
Loncar, Shannon M. ;
Fridman, Wolf Herman ;
Sautes-Fridman, Catherine .
DERMATOLOGY RESEARCH AND PRACTICE, 2010, 2010