Biomaterial-based vaccine induces regression of established intracranial glioma in rats.

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 (1 week) 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 > 100 days. 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.

journal_name

Pharm Res

journal_title

Pharmaceutical research

authors

Ali OA,Doherty E,Bell WJ,Fradet T,Hudak J,Laliberte MT,Mooney DJ,Emerich DF

doi

10.1007/s11095-010-0361-x

subject

Has Abstract

pub_date

2011-05-01 00:00:00

pages

1074-80

issue

5

eissn

0724-8741

issn

1573-904X

journal_volume

28

pub_type

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