TY - JOUR
T1 - Whole orbital tissue culture identifies imatinib mesylate and adalimumab as potential therapeutics for Graves' ophthalmopathy
AU - van Steensel, Leendert
AU - van Hagen, P Martin
AU - Paridaens, Dion
AU - Kuijpers, Robert W A M
AU - van den Bosch, Willem A
AU - Drexhage, Hemmo A
AU - Hooijkaas, Herbert
AU - Dik, Willem A
PY - 2011/5
Y1 - 2011/5
N2 - BACKGROUND AND AIMS: Biologicals and small inhibitory molecules are used to treat inflammatory diseases, but their efficacy varies upon clinical application. Using a whole orbital tissue culture system, we tested the potential efficacy of imatinib mesylate (a tyrosine kinase inhibitor that blocks platelet-derived growth factor (PDGF)-receptor, c-Abl and c-Kit activity) and adalimumab (an anti-TNF-α antibody) for the treatment of Graves' ophthalmopathy (GO).METHODS: Orbital fat tissue from GO patients (n=10) was cultured with or without imatinib mesylate or adalimumab. PDGF-B and tumour necrosis factor (TNF)-α mRNA expression levels were determined in the primary orbital tissue, and interleukin (IL)-6 and hyaluronan were measured in tissue-culture supernatants.RESULTS: Imatinib mesylate significantly (p=0.005) reduced IL-6 and hyaluronan production. The inhibition of hyaluronan production correlated positively and significantly (p<0.05) with the PDGF-B mRNA level in the primary tissue. Adalimumab also significantly (p=0.005) reduced IL-6 production. The amount of IL-6 inhibition correlated positively with the TNF-α mRNA level in the primary tissue, but this was not significant.CONCLUSIONS: Imatinib mesylate can be expected to reduce inflammation and tissue remodelling in GO, while adalimumab can be mainly expected to reduce inflammation. This in vitro tissue-culture model may, in future, prove valuable to test novel therapeutics for their presumed effect in GO as well as in other inflammatory diseases.
AB - BACKGROUND AND AIMS: Biologicals and small inhibitory molecules are used to treat inflammatory diseases, but their efficacy varies upon clinical application. Using a whole orbital tissue culture system, we tested the potential efficacy of imatinib mesylate (a tyrosine kinase inhibitor that blocks platelet-derived growth factor (PDGF)-receptor, c-Abl and c-Kit activity) and adalimumab (an anti-TNF-α antibody) for the treatment of Graves' ophthalmopathy (GO).METHODS: Orbital fat tissue from GO patients (n=10) was cultured with or without imatinib mesylate or adalimumab. PDGF-B and tumour necrosis factor (TNF)-α mRNA expression levels were determined in the primary orbital tissue, and interleukin (IL)-6 and hyaluronan were measured in tissue-culture supernatants.RESULTS: Imatinib mesylate significantly (p=0.005) reduced IL-6 and hyaluronan production. The inhibition of hyaluronan production correlated positively and significantly (p<0.05) with the PDGF-B mRNA level in the primary tissue. Adalimumab also significantly (p=0.005) reduced IL-6 production. The amount of IL-6 inhibition correlated positively with the TNF-α mRNA level in the primary tissue, but this was not significant.CONCLUSIONS: Imatinib mesylate can be expected to reduce inflammation and tissue remodelling in GO, while adalimumab can be mainly expected to reduce inflammation. This in vitro tissue-culture model may, in future, prove valuable to test novel therapeutics for their presumed effect in GO as well as in other inflammatory diseases.
KW - Adalimumab
KW - Antibodies, Monoclonal/therapeutic use
KW - Antibodies, Monoclonal, Humanized
KW - Benzamides
KW - Female
KW - Gene Expression Regulation/immunology
KW - Graves Ophthalmopathy/drug therapy
KW - Humans
KW - Hyaluronic Acid/biosynthesis
KW - Imatinib Mesylate
KW - Interleukin-6/biosynthesis
KW - Male
KW - Piperazines/therapeutic use
KW - Pyrimidines/therapeutic use
KW - RNA, Messenger/biosynthesis
KW - Tissue Culture Techniques/methods
KW - Tumor Necrosis Factor-alpha/metabolism
U2 - 10.1136/bjo.2010.192302
DO - 10.1136/bjo.2010.192302
M3 - Article
C2 - 21310803
SN - 0007-1161
VL - 95
SP - 735
EP - 738
JO - British Journal of Ophthalmology
JF - British Journal of Ophthalmology
IS - 5
ER -