The targeted delivery of IL17 to the mouse tumor neo-vasculature enhances angiogenesis but does not reduce tumor growth rate

There has been a long controversy as to whether interleukin-17 (IL17) has an impact on tumor growth. In order to assess whether IL17 may affect tumor growth, it would be convenient to achieve high levels of this pro-inflammatory cytokine at the tumor neo-vasculature, since IL17 is known to promote a...

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Veröffentlicht in:Angiogenesis (London) 2012-03, Vol.15 (1), p.165-169
Hauptverfasser: Pasche, Nadine, Frey, Katharina, Neri, Dario
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Frey, Katharina
Neri, Dario
description There has been a long controversy as to whether interleukin-17 (IL17) has an impact on tumor growth. In order to assess whether IL17 may affect tumor growth, it would be convenient to achieve high levels of this pro-inflammatory cytokine at the tumor neo-vasculature, since IL17 is known to promote angiogenesis. Here, we have generated and tested in vivo a fusion protein, consisting of the F8 antibody (specific to the alternatively spliced EDA domain of fibronectin, a marker of angiogenesis) and of murine IL17 (mIL17). The resulting immunocytokine (termed F8-mIL17) was shown to selectively localize at the tumor neo-vasculature and to vigorously promote tumor angiogenesis, without however reducing or enhancing tumor growth rate both in immunocompetent and in immunodeficient mice.
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subjects Animals
Antibodies - immunology
Biological and medical sciences
Biomedical and Life Sciences
Biomedicine
Blood and lymphatic vessels
Blood vessels and receptors
Brief Communication
Cancer Research
Cardiology
Cardiology. Vascular system
Cell Biology
Cell Line
Cell Proliferation - drug effects
Cloning, Molecular
Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous
Drug Delivery Systems - methods
Fundamental and applied biological sciences. Psychology
Interleukin-17 - pharmacology
Interleukin-17 - therapeutic use
Medical sciences
Mice
Neoplasms - blood supply
Neoplasms - drug therapy
Neoplasms - pathology
Neovascularization, Pathologic - drug therapy
Neovascularization, Pathologic - pathology
Oncology
Ophthalmology
Recombinant Fusion Proteins - pharmacology
Recombinant Fusion Proteins - therapeutic use
Subcutaneous Tissue - drug effects
Subcutaneous Tissue - pathology
Vertebrates: cardiovascular system
title The targeted delivery of IL17 to the mouse tumor neo-vasculature enhances angiogenesis but does not reduce tumor growth rate
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