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Stereotactic Adoptive Transfer of Cytotoxic Immune Cells in Murine Models of Orthotopic Human Glioblastoma Multiforme Xenografts
Published on: September 1, 2018
New agents for targeting of IL-13RA2 expressed in primary human and canine brain tumors
Waldemar Debinski1, Peter Dickinson, John H Rossmeisl
1The Brain Tumor Center of Excellence, Thomas K. Hearn Brain Tumor Research Center, Departments of Neurosurgery, Radiation Oncology, Wake Forest School of Medicine, Winston-Salem, North Carolina, United States of America.
Abstract:
Interleukin 13 receptor alpha 2 (IL-13RA2) is over-expressed in a vast majority of human patients with high-grade astrocytomas like glioblastoma. Spontaneous astrocytomas in dogs resemble human disease and have been proposed as translational model system for investigation of novel therapeutic strategies for brain tumors. We have generated reagents for both detection and therapeutic targeting of IL-13RA2 in human and canine brain tumors. Peptides from three different regions of IL-13RA2 with 100% sequence identity between human and canine receptors were used as immunogens for generation of monoclonal antibodies. Recombinant canine mutant IL-13 (canIL-13.E13K) and canIL-13.E13K based cytotoxin were also produced. The antibodies were examined for their immunoreactivities in western blots, immunohistochemistry, immunofluorescence and cell binding assays using human and canine tumor specimen sections, tissue lysates and established cell lines; the cytotoxin was tested for specific cell killing. Several isolated MAbs were immunoreactive to IL-13RA2 in western blots of cell and tissue lysates from glioblastomas from both human and canine patients. Human and canine astrocytomas and oligodendrogliomas were also positive for IL-13RA2 to various degrees. Interestingly, both human and canine meningiomas also exhibited strong reactivity. Normal human and canine brain samples were virtually negative for IL-13RA2 using the newly generated MAbs. MAb 1E10B9 uniquely worked on tissue specimens and western blots, bound live cells and was internalized in GBM cells over-expressing IL-13RA2. The canIL-13.E13K cytotoxin was very potent and specific in killing canine GBM cell lines. Thus, we have obtained several monoclonal antibodies against IL-13RA2 cross-reacting with human and canine receptors. In addition to GBM, other brain tumors, such as high grade oligodendrogliomas, meningiomas and canine choroid plexus papillomas, appear to express the receptor at high levels and thus may be appropriate candidates for IL-13RA2-targeted imaging/therapies. Canine spontaneous primary brain tumors represent an excellent translational model for human counterparts.
Insights
Researchers developed new tools to target Interleukin 13 receptor alpha 2 (IL-13RA2) in brain tumors. These reagents show promise for diagnosing and treating both human and canine glioblastomas and other brain cancers.
Area of Science:
- Neuro-oncology
- Immunology
- Comparative Medicine
Background:
- Interleukin 13 receptor alpha 2 (IL-13RA2) is highly expressed in human glioblastoma.
- Canine brain tumors serve as a valuable translational model for human diseases.
- Targeting IL-13RA2 offers a potential therapeutic strategy for brain tumors.
Purpose of the Study:
- To generate and characterize novel reagents for detecting and targeting IL-13RA2 in human and canine brain tumors.
- To evaluate the cross-reactivity of these reagents between human and canine IL-13RA2.
- To assess the therapeutic potential of a novel cytotoxin targeting IL-13RA2.
Main Methods:
- Development of monoclonal antibodies (mAbs) against IL-13RA2 using peptides with conserved sequences.
- Production of recombinant canine mutant IL-13 (canIL-13.E13K) and a corresponding cytotoxin.
- Immunoreactivity testing via Western blot, immunohistochemistry, immunofluorescence, and cell binding assays.
- Cytotoxicity assays to evaluate the efficacy of the canIL-13.E13K cytotoxin.
Main Results:
- Several mAbs demonstrated immunoreactivity to IL-13RA2 in both human and canine glioblastoma tissues and cell lines.
- IL-13RA2 expression was observed in human and canine astrocytomas, oligodendrogliomas, and meningiomas.
- Normal brain tissues showed minimal IL-13RA2 expression.
- MAb 1E10B9 exhibited strong binding to live cells and internalization in IL-13RA2-overexpressing glioblastoma cells.
- The canIL-13.E13K cytotoxin proved potent and specific in killing canine glioblastoma cell lines.
Conclusions:
- Novel monoclonal antibodies cross-reacting with human and canine IL-13RA2 have been successfully generated.
- IL-13RA2 is a promising target for imaging and therapy in various brain tumors, including glioblastoma, oligodendroglioma, and meningioma.
- Canine brain tumors represent an excellent translational model for developing IL-13RA2-targeted therapies for human brain cancer.

