64Cu-DOTA-Anti-CTLA-4 mAb Enabled PET Visualization of CTLA-4 on the T-Cell Infiltrating Tumor Tissues

被引:87
作者
Higashikawa, Kei [1 ,2 ]
Yagi, Katsuharu [1 ]
Watanabe, Keiko [1 ]
Kamino, Shinichiro [3 ]
Ueda, Masashi [1 ]
Hiromura, Makoto [3 ]
Enomoto, Shuichi [1 ,3 ]
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Okayama, Japan
[2] Japan Soc Promot Sci, Tokyo, Japan
[3] RIKEN, Ctr Life Sci Technol, Next Generat Imaging Team, Kobe, Hyogo, Japan
基金
日本学术振兴会;
关键词
MONOCLONAL-ANTIBODY; CANCER-IMMUNOTHERAPY; AUTOIMMUNE-DISEASE; ANTITUMOR-ACTIVITY; IMMUNE-SYSTEM; BIODISTRIBUTION; IPILIMUMAB; EXPRESSION; RESPONSES; SIGNALS;
D O I
10.1371/journal.pone.0109866
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) targeted therapy by anti-CTLA-4 monoclonal antibody (mAb) is highly effective in cancer patients. However, it is extremely expensive and potentially produces autoimmune-related adverse effects. Therefore, the development of a method to evaluate CTLA-4 expression prior to CTLA-4-targeted therapy is expected to open doors to evidence-based and cost-efficient medical care and to avoid adverse effects brought about by ineffective therapy. In this study, we aimed to develop a molecular imaging probe for CTLA-4 visualization in tumor. First, we examined CTLA-4 expression in normal colon tissues, cultured CT26 cells, and CT26 tumor tissues from tumor-bearing BALB/c mice and BALB/c nude mice by reverse transcription polymerase chain reaction (RT-PCR) analysis and confirmed whether CTLA-4 is strongly expressed in CT26 tumor tissues. Second, we newly synthesized Cu-64-1,4,7,10-tetraazacyclododecane-N,N',N '',N'''-tetraacetic acid-anti-mouse CTLA-4 mAb (Cu-64-DOTA-anti-CTLA-4 mAb) and evaluated its usefulness in positron emission tomography (PET) and ex-vivo biodistribution analysis in CT26-bearing BALB/c mice. High CTLA-4 expression was confirmed in the CT26 tumor tissues of tumor-bearing BALB/c mice. However, CTLA-4 expression was extremely low in the cultured CT26 cells and the CT26 tumor tissues of tumor-bearing BALB/c nude mice. The results suggested that T cells were responsible for the high CTLA-4 expression. Furthermore, Cu-64-DOTA-anti-CTLA-4 mAb displayed significantly high accumulation in the CT26 tumor, thereby realizing non-invasive CTLA-4 visualization in the tumor. Together, the results indicate that Cu-64-DOTA-anti-CTLA-4 mAb would be useful for the evaluation of CTLA-4 expression in tumor.
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页数:8
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