Neural Stem Cells as a Novel Platform for Tumor-Specific Delivery of Therapeutic Antibodies 英文参考文献.docVIP
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Neural Stem Cells as a Novel Platform for Tumor-Specific Delivery of Therapeutic Antibodies 英文参考文献
NeuralStemCellsasaNovelPlatformforTumor-Specific
DeliveryofTherapeuticAntibodies
RichardT.Frank1*,MarissaEdmiston1,StephenE.Kendall2,JosephNajbauer1,Chia-WeiCheung3,
ThewodrosKassa3,MarianneZ.Metz1,SeungU.Kim6,7,CarlottaA.Glackin2,AnnaM.Wu5,PaulJ.
Yazaki3,KarenS.Aboody1,4*
1DivisionsofHematologyandHematopoieticCellTransplantation,CityofHopeNationalMedicalCenterandBeckmanResearchInstitute,Duarte,California,UnitedStates
ofAmerica, 2Department ofMolecular Medicine,City ofHope NationalMedical Center and Beckman Research Institute, Duarte, California, United States ofAmerica,
3DepartmentofCancerImmunotherapyandTumorImmunology,CityofHopeNationalMedicalCenterandBeckmanResearchInstitute,Duarte,California,UnitedStates
of America, 4Department of Neurosciences, City of Hope National Medical Center and Beckman Research Institute, Duarte, California, United States of America,
5DepartmentofMolecularandMedicalPharmacology,DavidGeffenSchoolofMedicine,UniversityofCaliforniaLosAngeles,LosAngeles,California,UnitedStatesof
America,6DivisionofNeurology,DepartmentofMedicine,UBCHospital,UniversityofBritishColumbia,Vancouver,BritishColumbia,Canada,7InstituteforRegenerative
Medicine,GachonUniversityGilHospital,Inchon,Korea
Abstract
Background: Recombinant monoclonal antibodies have emerged as important tools for cancer therapy. Despite the
promise shown by antibody-based therapies, the large molecular size of antibodies limits their ability to efficiently
penetratesolidtumorsandprecludesefficientcrossingoftheblood-brain-barrier intothecentralnervoussystem (CNS).
Consequently,poorlyvascularizedsolidtumorsandCNSmetastasescannotbeeffectivelytreatedbyintravenously-injected
antibodies. The inherent tumor-tropic properties of human neural stem cells (NSCs) can potentially be harnessed to
overcome these obstacles and significantly improve cancer immunotherapy. Intravenously-delivered NSCs preferentially
migratetoprimary andmetastatic tumorsiteswithinandoutsidetheCNS.Therefore,wehypothes
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