TY - JOUR
T1 - Targeted delivery of IFNγ to tumor vessels uncouples antitumor from counterregulatory mechanisms
AU - Curnis, Flavio
AU - Gasparri, Anna
AU - Sacchi, Angelina
AU - Cattaneo, Angela
AU - Magni, Fulvio
AU - Corti, Angelo
PY - 2005/4/1
Y1 - 2005/4/1
N2 - Because of its immunomodulatory and anticancer activities, IFNγ has been used as an anticancer drug in several clinical studies, unfortunately with modest results. Attempts to increase the response by increasing the dose or by repeated continuous injection often resulted in lower efficacy, likely due to counterregulatory effects. We show here that targeted delivery of low doses of IFNγ CD13, a marker of angiogenic vessels, can overcome major counterregulatory mechanisms and delay tumor growth in two murine models that respond poorly to IFNγ. Tumor vascular targeting was achieved by coupling IFNγ to GCNGRC, a CD13 ligand, by genetic engineering technology. The dose-response curve was bell-shaped. Maximal effects were induced with a dose of 0.005 μg/kg, about 500-fold lower than the dose used in patients. Nontargeted IFNγ induced little or no effects over a range of 0.003 to 250 μg/kg. Studies on the mechanism of action showed that low doses of targeted IFNγ could activate tumor necrosis factor (TNF)-dependent antitumor mechanisms, whereas high doses of either targeted or nontargeted IFNγ induced soluble TNF-receptor shedding in circulation, a known counterregulatory mechanism of TNF activity. These findings suggest that antitumor activity and counterregulatory mechanisms could be uncoupled by tumor vascular targeting with extremely low doses of IFNγ.
AB - Because of its immunomodulatory and anticancer activities, IFNγ has been used as an anticancer drug in several clinical studies, unfortunately with modest results. Attempts to increase the response by increasing the dose or by repeated continuous injection often resulted in lower efficacy, likely due to counterregulatory effects. We show here that targeted delivery of low doses of IFNγ CD13, a marker of angiogenic vessels, can overcome major counterregulatory mechanisms and delay tumor growth in two murine models that respond poorly to IFNγ. Tumor vascular targeting was achieved by coupling IFNγ to GCNGRC, a CD13 ligand, by genetic engineering technology. The dose-response curve was bell-shaped. Maximal effects were induced with a dose of 0.005 μg/kg, about 500-fold lower than the dose used in patients. Nontargeted IFNγ induced little or no effects over a range of 0.003 to 250 μg/kg. Studies on the mechanism of action showed that low doses of targeted IFNγ could activate tumor necrosis factor (TNF)-dependent antitumor mechanisms, whereas high doses of either targeted or nontargeted IFNγ induced soluble TNF-receptor shedding in circulation, a known counterregulatory mechanism of TNF activity. These findings suggest that antitumor activity and counterregulatory mechanisms could be uncoupled by tumor vascular targeting with extremely low doses of IFNγ.
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U2 - 10.1158/0008-5472.CAN-04-4282
DO - 10.1158/0008-5472.CAN-04-4282
M3 - Article
C2 - 15805293
AN - SCOPUS:16844363607
VL - 65
SP - 2906
EP - 2913
JO - Journal of Cancer Research
JF - Journal of Cancer Research
SN - 0008-5472
IS - 7
ER -