Lack of in Vivo Antibody Dependent Cellular Cytotoxicity with Antibody Containing Gold Nanoparticles

被引:20
|
作者
Ahmed, Marya [1 ]
Pan, Dorothy W. [1 ]
Davis, Mark E. [1 ]
机构
[1] CALTECH, Chem Engn, Pasadena, CA 91125 USA
基金
加拿大自然科学与工程研究理事会;
关键词
GROWTH-FACTOR RECEPTOR; WILD-TYPE; CANCER; CETUXIMAB; EGFR;
D O I
10.1021/acs.bioconjchem.5b00139
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Antibody-dependent cellular cytotoxicity (ADCC) is a cytolytic mechanism that can elicit in vivo antitumor effects and can play a significant role in the efficacy of antibody treatments for cancer. Here, we prepared cetuximab, panitumumab, and rituximab containing gold nanoparticles and investigated their ability to produce an ADCC effect in vivo. Cetuximab treatment of EGFR-expressing H1975 tumor xenografts showed significant tumor regression due to the ADCC activity of the antibody in vivo, while the control antibody, panitumumab, did not. However, all three antibody containing nanoparticles are not able to suppress tumor growth in the same in vivo mouse model. The antibody containing nanoparticles localized in the tumors and did not suppress the immune function Of the animals, so the lack of tumor growth suppression of the cetuximab containing nanoparticle suggests that immobilizing antibodies onto a nanoparticle significantly decreases the ability of the antibody to promote an ADCC response.
引用
收藏
页码:812 / 816
页数:5
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