Biological Evaluation of 131I- and CF750-Labeled Dmab(scFv)-Fc Antibodies for Xenograft Imaging of CD25-Positive Tumors

被引:17
作者
Fan, Qing [1 ]
Cai, Huawei [2 ]
Yang, Hao [1 ]
Li, Lin [2 ]
Yuan, Cen [2 ]
Lu, Xiaofeng [1 ]
Wan, Lin [1 ]
机构
[1] Sichuan Univ, Lab Transplant Engn & Immunol, Regenerat Med Res Ctr, West China Hosp, Chengdu 610041, Peoples R China
[2] Sichuan Univ, Dept Nucl Med, West China Hosp, Chengdu 610041, Peoples R China
关键词
CELL; LEUKEMIA; EXPRESSION; FRAGMENTS; THERAPY; PROGRESS;
D O I
10.1155/2014/459676
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
A Dmab(scFv)-Fc antibody containing the single chain variable fragment of a humanized daclizumab antibody and the Fc fragment of a human IgG1 antibody was produced via recombinant expression in Pichia pastoris. The Dmab(scFv)-Fc antibody forms a dimer in solution, and it specifically binds CD25-positive tumor cells and tumor tissues. For tumor imaging, the Dmab(scFv)-Fc antibody was labeled with the 131I isotope and CF750 fluorescent dye, respectively. After intravenous injection of mice bearing CD25-positive tumor xenografts, tumor uptake of the I-131-Dmab(scFv)-Fc antibody was visible at 1 h, and clear images were obtained at 5 h using SPECT/CT. After systemic administration of the CF750-Dmab(scFv)-Fc antibody, tumor uptake was present as early as 1 h, and tumor xenografts could be kinetically imaged within 9 h after injection. These results indicate that the Dmab(scFv)-Fc antibody rapidly and specifically targets CD25-positive tumor cells, suggesting the potential of this antibody as an imaging agent for the diagnosis of lymphomatous-type ATLL.
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页数:11
相关论文
共 35 条
[11]   Antibody therapy for Adult T-cell leukemia-lymphoma [J].
Ishida, Takashi ;
Ueda, Ryuzo .
INTERNATIONAL JOURNAL OF HEMATOLOGY, 2011, 94 (05) :443-452
[12]   Novel Human Single Chain Antibody Fragments That Are Rapidly Internalizing Effectively Target Epithelioid and Sarcomatoid Mesotheliomas [J].
Iyer, Arun K. ;
Lan, Xiaoli ;
Zhu, Xiaodong ;
Su, Yang ;
Feng, Jinjin ;
Zhang, Xiaoju ;
Gao, Dongwei ;
Seo, Youngho ;
VanBrocklin, Henry F. ;
Broaddus, V. Courtney ;
Liu, Bin ;
He, Jiang .
CANCER RESEARCH, 2011, 71 (07) :2428-2432
[13]   Optimizing Therapeutic Antibody Function Progress with Fc Domain Engineering [J].
Kaneko, Etsuji ;
Niwa, Rinpei .
BIODRUGS, 2011, 25 (01) :1-11
[14]   Recent trends in antibody-based oncologic imaging [J].
Kaur, Sukhwinder ;
Venktaraman, Ganesh ;
Jain, Maneesh ;
Senapati, Shantibhusan ;
Garg, Pradeep K. ;
Batra, Surinder K. .
CANCER LETTERS, 2012, 315 (02) :97-111
[15]   The progress and promise of molecular imaging probes in oncologic drug development [J].
Kelloff, GJ ;
Krohn, KA ;
Larson, SM ;
Weissleder, R ;
Mankoff, DA ;
Hoffman, JM ;
Link, JM ;
Guyton, KZ ;
Eckelman, WC ;
Scher, HI ;
O'Shaughnessy, J ;
Cheson, BD ;
Sigman, CC ;
Tatum, JL ;
Mills, GQ ;
Sullivan, DC ;
Woodcock, J .
CLINICAL CANCER RESEARCH, 2005, 11 (22) :7967-7985
[16]   Radioiodinated versus radiometal-labeled anti-carcinoembryonic antigen single-chain Fv-Fc antibody fragments: Optimal pharmacokinetics for therapy [J].
Kenanova, Vania ;
Olafsen, Tove ;
Williams, Lawrence E. ;
Ruel, Nora H. ;
Longmate, Jeffrey ;
Yazaki, Paul J. ;
Shively, John E. ;
Colcher, David ;
Raubitschek, Andrew A. ;
Wu, Anna M. .
CANCER RESEARCH, 2007, 67 (02) :718-726
[17]  
KIKUCHI M, 2001, WHO CLASSIFICATION T, P200
[18]   Engineered humanized diabodies for microPET imaging of prostate stem cell antigen-expressing tumors [J].
Leyton, Jeffrey V. ;
Olafsen, Tove ;
Sherman, Mark A. ;
Bauer, Karl B. ;
Aghajanian, Patrick ;
Reiter, Robert E. ;
Wu, Anna M. .
PROTEIN ENGINEERING DESIGN & SELECTION, 2009, 22 (03) :209-216
[19]   A review of NIR dyes in cancer targeting and imaging [J].
Luo, Shenglin ;
Zhang, Erlong ;
Su, Yongping ;
Cheng, Tianmin ;
Shi, Chunmeng .
BIOMATERIALS, 2011, 32 (29) :7127-7138
[20]   Adult T-cell leukaemia/lymphoma [J].
Matutes, E. .
JOURNAL OF CLINICAL PATHOLOGY, 2007, 60 (12) :1373-1377