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Cellular-Based Immunotherapies for Patients with Glioblastoma Multiforme英文文献资料
HindawiPublishingCorporation
ClinicalandDevelopmentalImmunology
Volume2012,ArticleID764213,15pages
doi:10.1155/2012/764213
ReviewArticle
Cellular-BasedImmunotherapiesforPatientswith
GlioblastomaMultiforme
XunXu, FlorianStockhammer, andMichaelSchmitt
1 2 3
1
Center for Biomaterial Development and Berlin-Brandenburg Center for Regenerative Therapies, Institute of Polymer Research,
Helmholtz-ZentrumGeesthacht,14513Teltow,Germany
2
3
DepartmentofNeurosurgery,UniversityofG¨ottingen,37073G¨ottingen,Germany
DepartmentofInternalMedicineV,Hematology,OncologyandRheumatology,UniversityofHeidelberg,69120Heidelberg,Germany
CorrespondenceshouldbeaddressedtoMichaelSchmitt,michael.schmitt@med.uni-heidelberg.de
Received7November2011;Accepted8December2011
AcademicEditor:LucaGattinoni
Copyright?2012XunXuetal.ThisisanopenaccessarticledistributedundertheCreativeCommonsAttributionLicense,which
permitsunrestricteduse,distribution,andreproductioninanymedium,providedtheoriginalworkisproperlycited.
Treatmentofpatientswithglioblastomamultiforme(GBM)remainstobeachallengewithamediansurvivalof14.6months
following diagnosis. Standard treatment options include surgery, radiation therapy, and systemic chemotherapy with
temozolomide.Despitethefactthatthebrainconstitutesanimmunoprivilegedsite,recentobservationsafterimmunotherapies
withlysatefromautologoustumorcellspulsedondendriticcells(DCs),peptides,protein,messengerRNA,andcytokinessuggest
animmunologicalandevenclinicalresponsefromimmunotherapies.Giventhisplethoraofimmunomodulatorytherapies,this
papergivesastructureoverviewofthestate-of-theartinthe?eld.Particularemphasiswasalsoputonimmunogenicantigensas
potentialtargetsforamorespeci?cstimulationoftheimmunesystemagainstGBM.
1.Introduction
noncontrast enhancing tumor part and can be visualized
by aminoacid positron emission tomography [5]. Placing
carmustine-loadedwafersintheresectioncavityhasshown
to prolong survival rates [6]. However, the clinical bene?
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