Single vs. combination immunotherapeutic strategies for glioma

被引:21
作者
Chandran, Mayuri [1 ,2 ]
Candolfi, Marianela [3 ]
Shah, Diana [1 ,2 ]
Mineharu, Yohei [4 ]
Yadav, Viveka Nand [1 ,2 ]
Koschmann, Carl [1 ,5 ]
Asad, Antonela S. [3 ]
Lowenstein, Pedro R. [1 ,2 ]
Castro, Maria G. [1 ,2 ]
机构
[1] Univ Michigan, Sch Med, Dept Neurosurg, MSRB 2, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Cell & Dev Biol, Sch Med, Ann Arbor, MI USA
[3] Univ Buenos Aires, Inst Invest Biomed CONICET UBA, Fac Med, Buenos Aires, DF, Argentina
[4] Kyoto Univ, Dept Neurosurg, Grad Sch Med, Kyoto, Japan
[5] Univ Michigan, Sch Med, Dept Pediat Hematol & Oncol, Ann Arbor, MI USA
基金
美国国家卫生研究院;
关键词
Glioma; immunotherapy; gene therapy; cancer vaccines; immune checkpoint blockade; DENDRITIC CELL VACCINATION; REGULATORY T-CELLS; CENTRAL-NERVOUS-SYSTEM; GROWTH-FACTOR RECEPTOR; I CLINICAL-TRIAL; GENE-THERAPY; PEPTIDE VACCINATION; GM-CSF; ADULT GLIOBLASTOMA; SUPPRESSOR-CELLS;
D O I
10.1080/14712598.2017.1305353
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: Malignant gliomas are highly invasive tumors, associated with a dismal survival rate despite standard of care, which includes surgical resection, radiotherapy and chemotherapy with temozolomide (TMZ). Precision immunotherapies or combinations of immunotherapies that target unique tumor-specific features may substantially improve upon existing treatments.Areas covered: Clinical trials of single immunotherapies have shown therapeutic potential in high-grade glioma patients, and emerging preclinical studies indicate that combinations of immunotherapies may be more effective than monotherapies. In this review, the authors discuss emerging combinations of immunotherapies and compare efficacy of single vs. combined therapies tested in preclinical brain tumor models.Expert opinion: Malignant gliomas are characterized by a number of factors which may limit the success of single immunotherapies including inter-tumor and intra-tumor heterogeneity, intrinsic resistance to traditional therapies, immunosuppression, and immune selection for tumor cells with low antigenicity. Combination of therapies which target multiple aspects of tumor physiology are likely to be more effective than single therapies. While a limited number of combination immunotherapies are described which are currently being tested in preclinical and clinical studies, the field is expanding at an astounding rate, and endless combinations remain open for exploration.
引用
收藏
页码:543 / 554
页数:12
相关论文
共 111 条
[1]   Gene therapy enhances chemotherapy tolerance and efficacy in glioblastoma patients [J].
Adair, Jennifer E. ;
Johnston, Sandra K. ;
Mrugala, Maciej M. ;
Beard, Brian C. ;
Guyman, Laura A. ;
Baldock, Anne L. ;
Bridge, Carly A. ;
Hawkins-Daarud, Andrea ;
Gori, Jennifer L. ;
Born, Donald E. ;
Gonzalez-Cuyar, Luis F. ;
Silbergeld, Daniel L. ;
Rockne, Russell C. ;
Storer, Barry E. ;
Rockhill, Jason K. ;
Swanson, Kristin R. ;
Kiem, Hans-Peter .
JOURNAL OF CLINICAL INVESTIGATION, 2014, 124 (09) :4082-4092
[2]   Extended Survival of Glioblastoma Patients After Chemoprotective HSC Gene Therapy [J].
Adair, Jennifer E. ;
Beard, Brian C. ;
Trobridge, Grant D. ;
Neff, Tobias ;
Rockhill, Jason K. ;
Silbergeld, Daniel L. ;
Mrugala, Maciej M. ;
Kiem, Hans-Peter .
SCIENCE TRANSLATIONAL MEDICINE, 2012, 4 (133)
[3]   Sequential Immunotherapy by Vaccination With GM-CSF-expressing Glioma Cells and CTLA-4 Blockade Effectively Treats Established Murine Intracranial Tumors [J].
Agarwalla, Pankaj ;
Barnard, Zachary ;
Fecci, Peter ;
Dranoff, Glenn ;
Curry, William T., Jr. .
JOURNAL OF IMMUNOTHERAPY, 2012, 35 (05) :385-389
[4]   Biomarker-driven diagnosis of diffuse gliomas [J].
Appin, Christina L. ;
Brat, Daniel J. .
MOLECULAR ASPECTS OF MEDICINE, 2015, 45 :87-96
[5]   mTOR regulates memory CD8 T-cell differentiation [J].
Araki, Koichi ;
Turner, Alexandra P. ;
Shaffer, Virginia Oliva ;
Gangappa, Shivaprakash ;
Keller, Susanne A. ;
Bachmann, Martin F. ;
Larsen, Christian P. ;
Ahmed, Rafi .
NATURE, 2009, 460 (7251) :108-U124
[6]   Mechanisms of Glioma Formation: Iterative Perivascular Glioma Growth and Invasion Leads to Tumor Progression, VEGF-Independent Vascularization, and Resistance to Antiangiogenic Therapy [J].
Baker, Gregory J. ;
Yadav, Viveka Nand ;
Motsch, Sebastien ;
Koschmann, Carl ;
Calinescu, Anda-Alexandra ;
Mineharu, Yohei ;
Camelo-Piragua, Sandra Ines ;
Orringer, Daniel ;
Bannykh, Serguei ;
Nichols, Wesley S. ;
deCarvalho, Ana C. ;
Mikkelsen, Tom ;
Castro, Maria G. ;
Lowenstein, Pedro R. .
NEOPLASIA, 2014, 16 (07) :543-561
[7]   One-year expression from high-capacity adenoviral vectors in the brains of animals with pre-existing anti-adenoviral immunity: Clinical implications [J].
Barcia, Carlos ;
Jimenez-Dalmaroni, Maximiliano ;
Kroeger, Kurt M. ;
Puntel, Mariana ;
Rapaport, Alison J. ;
Larocque, Daniel ;
King, Gwendalyn D. ;
Johnson, Stephen A. ;
Liu, Chunyan ;
Xiong, Weidong ;
Candolfi, Marianela ;
Mondkar, Sonali ;
Ng, Philip ;
Palmer, Donna ;
Castro, Maria G. ;
Lowenstein, Pedro R. .
MOLECULAR THERAPY, 2007, 15 (12) :2154-2163
[8]  
Barcia C, 2006, J EXP MED, V203, P2095, DOI 10.1084/jem.20060420
[9]   Programmed death ligand 1 expression and tumor-infiltrating lymphocytes in glioblastoma [J].
Berghoff, Anna Sophie ;
Kiesel, Barbara ;
Widhalm, Georg ;
Rajky, Orsolya ;
Ricken, Gerda ;
Woehrer, Adelheid ;
Dieckmann, Karin ;
Filipits, Martin ;
Brandstetter, Anita ;
Weller, Michael ;
Kurscheid, Sebastian ;
Hegi, Monika E. ;
Zielinski, Christoph C. ;
Marosi, Christine ;
Hainfellner, Johannes A. ;
Preusser, Matthias ;
Wick, Wolfgang .
NEURO-ONCOLOGY, 2015, 17 (08) :1064-1075
[10]   Immunotherapy for cancer in the central nervous system: Current and future directions [J].
Binder, David C. ;
Davis, Andrew A. ;
Wainwright, Derek A. .
ONCOIMMUNOLOGY, 2016, 5 (02)