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   <subfield code="a">Biomaterial-Based Vaccine Induces Regression of Established Intracranial Glioma in Rats</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Omar Ali, Ed Doherty, William Bell, Tracie Fradet, Jebecka Hudak, Marie-Therese Laliberte, David Mooney, Dwaine Emerich]</subfield>
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   <subfield code="a">ABSTRACT: Purpose: The prognosis for glioma patients is poor, and development of new treatments is critical. Previously, we engineered polymer-based vaccines that control GM-CSF, CpG-oligonucleotide, and tumor-lysate presentation to regulate immune cell trafficking and activation, which promoted potent immune responses against peripheral tumors. Here, we extend the use of this system to glioma. Methods: Rats were challenged with an intracranial injection of glioma cells followed (1week) by administration of the polymeric vaccine (containing GM-CSF, CpG, and tumor-lysate) in the tumor bed. Control rats were treated with blank matrices, matrices with GM-CSF and CpG, or intra-tumoral bolus injections of GM-CSF, CpG, and tumor lysate. Rats were monitored for survival and tested for neurological function. Results: Survival studies confirmed a benefit of the polymeric vaccine as 90% of vaccinated rats survived for &gt;100days. Control rats exhibited minimal benefit. Motor tests revealed that vaccination protected against the loss of forelimb use produced by glioma growth. Histological analysis quantitatively confirmed a robust and rapid reduction in tumor size. Long-term immunity was confirmed when 67% of survivors also survived a second glioma challenge. Conclusions: These studies extend previous reports regarding this approach to tumor therapy and justify further development for glioma treatment.</subfield>
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   <subfield code="a">Springer Science+Business Media, LLC, 2011</subfield>
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