Oncolytic Virotherapy for Hematological Malignancies

被引:29
作者
Bais, Swarna [1 ]
Bartee, Eric [2 ]
Rahman, Masmudur M. [2 ]
McFadden, Grant [2 ]
Cogle, Christopher R. [1 ]
机构
[1] Univ Florida, Coll Med, Dept Med, Div Hematol & Oncol, Gainesville, FL 32610 USA
[2] Univ Florida, Coll Med, Dept Mol Genet & Microbiol, ARB R4-295,POB 100266, Gainesville, FL 32610 USA
关键词
D O I
10.1155/2012/186512
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Hematological malignancies such as leukemias, lymphomas, multiple myeloma (MM), and the myelodysplastic syndromes (MDSs) primarily affect adults and are difficult to treat. For high-risk disease, hematopoietic stem cell transplant (HCT) can be used. However, in the setting of autologous HCT, relapse due to contamination of the autograft with cancer cells remains a major challenge. Ex vivo manipulations of the autograft to purge cancer cells using chemotherapies and toxins have been attempted. Because these past strategies lack specificity for malignant cells and often impair the normal hematopoietic stem and progenitor cells, prior efforts to ex vivo purge autografts have resulted in prolonged cytopenias and graft failure. The ideal ex vivo purging agent would selectively target the contaminating cancer cells while spare normal stem and progenitor cells and would be applied quickly without toxicities to the recipient. One agent which meets these criteria is oncolytic viruses. This paper details experimental progress with reovirus, myxoma virus, measles virus, vesicular stomatitis virus, coxsackievirus, and vaccinia virus as well as requirements for translation of these results to the clinic.
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页数:8
相关论文
共 77 条
[1]   Autologous transplantation of mobilized peripheral blood CD34+ cells selected by immunomagnetic procedures in patients with multiple myeloma [J].
Abonour, R ;
Scott, KM ;
Kunkel, LA ;
Robertson, MJ ;
Hromas, R ;
Graves, V ;
Lazaridis, EN ;
Cripe, L ;
Gharpure, V ;
Traycoff, CM ;
Mills, B ;
Srour, EF ;
Cornetta, K .
BONE MARROW TRANSPLANTATION, 1998, 22 (10) :957-963
[2]  
Adachi Y, 2001, CANCER RES, V61, P7882
[3]   Reovirus therapy of lymphoid malignancies [J].
Alain, T ;
Hirasawa, K ;
Pon, KJ ;
Nishikawa, SG ;
Urbanski, SJ ;
Auer, Y ;
Luider, J ;
Martin, A ;
Johnston, RN ;
Janowska-Wieczorek, A ;
Lee, PWK ;
Kossakowska, AE .
BLOOD, 2002, 100 (12) :4146-4153
[4]  
American Cancer Society, 2011, CANC FACTS FIG 2015
[5]   Oncolytic Rat Parvovirus H-1PV, a Candidate for the Treatment of Human Lymphoma: In Vitro and In Vivo Studies [J].
Angelova, Assia L. ;
Aprahamian, Marc ;
Balboni, Ginette ;
Delecluse, Henri-Jacques ;
Feederle, Regina ;
Kiprianova, Irina ;
Grekova, Svitlana P. ;
Galabov, Angel S. ;
Witzens-Harig, Mathias ;
Ho, Anthony D. ;
Rommelaere, Jean ;
Raykov, Zahari .
MOLECULAR THERAPY, 2009, 17 (07) :1164-1172
[6]   Purging in BCR-ABL-positive acute lymphoblastic leukemia using immunomagnetic beads:: comparison of residual leukemia and purging efficiency in bone marrow vs peripheral blood stem cells by semiquantitative polymerase chain reaction [J].
Atta, J ;
Fauth, F ;
Keyser, M ;
Petershofen, E ;
Weber, C ;
Lippok, G ;
Hoelzer, D ;
Martin, H .
BONE MARROW TRANSPLANTATION, 2000, 25 (01) :97-104
[7]   Oncolytic Coxsackievirus A21 as a novel therapy for multiple myeloma [J].
Au, Gough G. ;
Lincz, Lisa F. ;
Enno, Arno ;
Shafren, Darren R. .
BRITISH JOURNAL OF HAEMATOLOGY, 2007, 137 (02) :133-141
[8]   Negative selection of peripheral blood stem cells to support a tandem autologous transplantation programme in multiple myeloma [J].
Barbui, AM ;
Galli, M ;
Dotti, G ;
Belli, N ;
Borleri, G ;
Gritti, G ;
Bellavita, P ;
Viero, P ;
Comotti, B ;
Barbui, T ;
Rambaldi, A .
BRITISH JOURNAL OF HAEMATOLOGY, 2002, 116 (01) :202-210
[9]   Long-Term Follow-Up of Autotransplantation Trials for Multiple Myeloma: Update of Protocols Conducted by the Intergroupe Francophone du Myelome, Southwest Oncology Group, and University of Arkansas for Medical Sciences [J].
Barlogie, Bart ;
Attal, Michel ;
Crowley, John ;
van Rhee, Frits ;
Szymonifka, Jackie ;
Moreau, Philippe ;
Durie, Brian G. M. ;
Harousseau, Jean-Luc .
JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (07) :1209-1214
[10]   Human cancer cells have specifically lost the ability to induce the synergistic state caused by tumor necrosis factor plus interferon-β [J].
Bartee, Eric ;
McFadden, Grant .
CYTOKINE, 2009, 47 (03) :199-205