| Literature DB >> 33395313 |
Jiaying Liu, Randall Toy, Casey Vantucci, Pallab Pradhan, Zijian Zhang, Katie M Kuo, Kelsey P Kubelick, Da Huo, Jianguo Wen1, Jinhwan Kim, Zhiheng Lyu, Simran Dhal, Alexandra Atalis, Shohini K Ghosh-Choudhary2, Emily J Devereaux3,4, James C Gumbart, Younan Xia, Stanislav Y Emelianov, Nick J Willett3,4, Krishnendu Roy.
Abstract
Monoclonal antibodies (mAb) have had a transformative impact on treating cancers and immune disorders. However, their use is limited by high development time and monetary cost, manufacturing complexities, suboptimal pharmacokinetics, and availability of disease-specific targets. To address some of these challenges, we developed an entirely synthetic, multivalent, Janus nanotherapeutic platform, called Synthetic Nanoparticle Antibodies (SNAbs). SNAbs, with phage-display-identified cell-targeting ligands on one "face" and Fc-mimicking ligands on the opposite "face", were synthesized using a custom, multistep, solid-phase chemistry method. SNAbs efficiently targeted and depleted myeloid-derived immune-suppressor cells (MDSCs) from mouse-tumor and rat-trauma models, ex vivo. Systemic injection of MDSC-targeting SNAbs efficiently depleted circulating MDSCs in a mouse triple-negative breast cancer model, enabling enhanced T cell and Natural Killer cell infiltration into tumors. Our results demonstrate that SNAbs are a versatile and effective functional alternative to mAbs, with advantages of a plug-and-play, cell-free manufacturing process, and high-throughput screening (HTS)-enabled library of potential targeting ligands.Entities:
Keywords: Janus nanoparticle; antibody-dependent cellular responses; immunotherapy; monoclonal antibody; myeloid-derived suppressor cell
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Year: 2021 PMID: 33395313 PMCID: PMC8176937 DOI: 10.1021/acs.nanolett.0c04833
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189