Cytokines: The Good, the Bad, and the Deadly

被引:78
作者
Ramani, Thulasi [1 ]
Auletta, Carol S. [1 ]
Weinstock, Daniel [2 ]
Mounho-Zamora, Barbara [3 ]
Ryan, Patricia C. [4 ]
Salcedo, Theodora W. [5 ]
Bannish, Gregory [1 ]
机构
[1] Huntingdon Life Sci, Somerset, NJ 08873 USA
[2] Janssen R&D LLC, Spring House, PA USA
[3] ToxStrategies Inc, Bend, OR USA
[4] MedImmune, Gaithersburg, MD USA
[5] Bristol Myers Squibb Co, New Brunswick, NJ USA
关键词
cytokines; biotherapeutics; immunomodulators; cytokine release syndrome; biomarkers; THERAPEUTIC MONOCLONAL-ANTIBODIES; REGULATORY T-CELLS; IN-VIVO TOXICITY; PRECLINICAL EFFICACY; EXPRESSION; RELEASE; TRIAL; VALIDATION; TGN1412; CD4(+);
D O I
10.1177/1091581815584918
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Over the past 30 years, the world of pharmaceutical toxicology has seen an explosion in the area of cytokines. An overview of the many aspects of cytokine safety evaluation currently in progress and evolving strategies for evaluating these important entities was presented at this symposium. Cytokines play a broad role to help the immune system respond to diseases, and drugs which modulate their effect have led to some amazing therapies. Cytokines may be good when stimulating the immune system to fight a foreign pathogen or attack tumors. Other good cytokine effects include reduction of an immune response, for example interferon reduction of neuron inflammation in patients with multiple sclerosis. They may be bad when their expression causes inflammatory diseases, such as the role of tumor necrosis factor alpha in rheumatoid arthritis or asthma and Crohn's disease. Therapeutic modulation of cytokine expression can help the good cytokines to generate or quench the immune system and block the bad cytokines to prevent damaging inflammatory events. However, care must be exercised, as some antibody therapeutics can cause ugly cytokine release which can be deadly. Well-designed toxicology studies should incorporate careful assessment of cytokine modulation that will allow effective therapies to treat unmet needs. This symposium discussed lessons learned in cytokine toxicology using case studies and suggested future directions.
引用
收藏
页码:355 / 365
页数:11
相关论文
共 45 条
[1]
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
[2]
Preclinical screening for acute toxicity of therapeutic monoclonal antibodies in a hu-SCID model [J].
Brady, Jamie L. ;
Harrison, Leonard C. ;
Goodman, David J. ;
Cowan, Peter J. ;
Hawthorne, Wayne J. ;
O'Connell, Philip J. ;
Sutherland, Robyn M. ;
Lew, Andrew M. .
CLINICAL & TRANSLATIONAL IMMUNOLOGY, 2014, 3
[3]
Longitudinal Cytokine Expression during IMRT for Prostate Cancer and Acute Treatment Toxicity [J].
Christensen, Eva ;
Pintilie, Melania ;
Evan, Kenneth R. ;
Lenarduzzi, Michelle ;
Menard, Cynthia ;
Catton, Charles N. ;
Diamandis, Eleftherios P. ;
Bristow, Robert G. .
CLINICAL CANCER RESEARCH, 2009, 15 (17) :5576-5583
[4]
Cytokine therapy [J].
Cutler, A ;
Brombacher, F .
NATURAL PRODUCTS AND MOLECULAR THERAPY, 2005, 1056 :16-29
[5]
Cytokines as Biomarkers of Treatment Response to IFN beta in Relapsing-Remitting Multiple Sclerosis [J].
Dimisianos, Nikolaos ;
Rodi, Maria ;
Kalavrizioti, Dimitra ;
Georgiou, Vasileios ;
Papathanasopoulos, Panagiotis ;
Mouzaki, Athanasia .
MULTIPLE SCLEROSIS INTERNATIONAL, 2014, 2014
[6]
Monoclonal antibody TGN1412 trial failure explained by species differences in CD28 expression on CD4+ effector memory T-cells [J].
Eastwood, D. ;
Findlay, L. ;
Poole, S. ;
Bird, C. ;
Wadhwa, M. ;
Moore, M. ;
Burns, C. ;
Thorpe, R. ;
Stebbings, R. .
BRITISH JOURNAL OF PHARMACOLOGY, 2010, 161 (03) :512-526
[7]
Cytokine release assays: Current practices and future directions [J].
Finco, D. ;
Grimaldi, C. ;
Fort, M. ;
Walker, M. ;
Kiessling, A. ;
Wolf, B. ;
Salcedo, T. ;
Faggioni, R. ;
Schneider, A. ;
Ibraghimov, A. ;
Scesney, S. ;
Serna, D. ;
Prell, R. ;
Stebbings, R. ;
Narayanan, P. K. .
CYTOKINE, 2014, 66 (02) :143-155
[8]
Comparison of novel methods for predicting the risk of pro-inflammatory clinical infusion reactions during monoclonal antibody therapy [J].
Findlay, Lucy ;
Eastwood, David ;
Ball, Christina ;
Robinson, C. Jane ;
Bird, Chris ;
Wadhwa, Meenu ;
Thorpe, Susan J. ;
Thorpe, Robin ;
Stebbings, Richard ;
Poole, Stephen .
JOURNAL OF IMMUNOLOGICAL METHODS, 2011, 371 (1-2) :134-142
[9]
Improved in vitro methods to predict the in vivo toxicity in man of therapeutic monoclonal antibodies including TGN1412 [J].
Findlay, Lucy ;
Eastwood, David ;
Stebbings, Richard ;
Sharp, Giles ;
Mistry, Yogesh ;
Ball, Christina ;
Hood, John ;
Thorpe, Robin ;
Poole, Stephen .
JOURNAL OF IMMUNOLOGICAL METHODS, 2010, 352 (1-2) :1-12
[10]
Predicting cytokine storms: it's about density [J].
Frigault, Matthew J. ;
June, Carl H. .
BLOOD, 2011, 118 (26) :6724-+