Blockade of CTLA-4 Increases Anti-Tumor Response Inducing Potential of Dendritic Cell Vaccine

Blockade of CTLA-4 Increases Anti-Tumor Response Inducing Potential of Dendritic Cell Vaccine


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نویسندگان: علی مسجدی , شاهین حلاج , فرهاد جدیدی نیارق

کلمات کلیدی: Colon cancer Dendritic cell vaccine CTLA-4 Immunotherapy Nanoparticles Chitosan lactate Drug delivery CT26 4 T1 Cell therapy

نشریه: 55299 , 1 , 326 , 2020

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نویسنده ثبت کننده مقاله فرهاد جدیدی نیارق
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه مرکز تحقیقات ایمونولوژی
کد مقاله 72271
عنوان فارسی مقاله Blockade of CTLA-4 Increases Anti-Tumor Response Inducing Potential of Dendritic Cell Vaccine
عنوان لاتین مقاله Blockade of CTLA-4 Increases Anti-Tumor Response Inducing Potential of Dendritic Cell Vaccine
ناشر 14
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ بلی
عنوان نشریه (خارج از لیست فوق)
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح یک – ISI - Web of Science
آدرس لینک مقاله/ همایش در شبکه اینترنت

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The immunosuppressive state of the tumor microenvironment diminishes the efficacy of dendritic cell (DC)-based cancer immunotherapy. Inhibitory immune checkpoint molecules expressed on tumor-infiltrating T lymphocytes, such as cytotoxic T-lymphocyte antigen 4 (CTLA-4) molecules are one of the main barriers in priming T cells by DCs. Therefore, it seems that blockade of such molecules facilitates the T cells activation by the DC vaccine. In this study, we intended to suppress the expression of CTLA-4 molecule on tumor-infiltrating T cells by siRNA-loaded chitosan-lactate (CL) nanoparticles to facilitate priming anti- tumor T cells by tumor lysate-loaded DC vaccine. Nanoparticles (NPs) have also provided an opportunity for specific drug delivery into the tumor site. CL NPs exhibited favorable physicochemical characteristics (size about 75 nm, polydispersive index<0.2, and a zeta potential about 14), which were associated with a high transfection rate and low toxicity. Moreover, the administration of anti-CTLA-4 siRNA-loaded NPs into CT26 and 4 T1 tumor -bearing mice led to the downregulation of CTLA-4 on tumor -infiltrating T cells, which was associated with tumor regression and increased mice survival. Moreover, while the treatment of tumor -bearing mice with DC vaccine had mild therapeutic outcomes, its combination with siRNA-loaded NPs may exhibit synergistic anti- tumor effects. This possible synergistic ameliorating effect is achieved through the reduction of immunosuppressive cells, the improved cytotoxicity of T lymphocytes, decreased inhibitory and increased inflammatory cytokines, and reduced angiogenesis and metastasis processes. These results indicate that the silencing of CTLA-4 can potentiate the T cell priming capacity of the DC vaccine, proposing a practical anti-cancer therapeutic approach.

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نویسنده نفر چندم مقاله
علی مسجدیدوم
شاهین حلاجسوم
فرهاد جدیدی نیارقچهاردهم

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Blockade of CTLA-4 increases anti-tumor response inducing potential of dendritic cell vaccine.pdf1399/04/063121243دانلود