Bifunctional Janus Particles as Multivalent Synthetic Nanoparticle Antibodies (SNAbs) for Selective Depletion of Target Cells.

Janus nanoparticle antibody-dependent cellular responses immunotherapy monoclonal antibody myeloid-derived suppressor cell

Journal

Nano letters
ISSN: 1530-6992
Titre abrégé: Nano Lett
Pays: United States
ID NLM: 101088070

Informations de publication

Date de publication:
13 01 2021
Historique:
pubmed: 5 1 2021
medline: 25 6 2021
entrez: 4 1 2021
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 33395313
doi: 10.1021/acs.nanolett.0c04833
pmc: PMC8176937
mid: NIHMS1705052
doi:

Substances chimiques

Antibodies, Monoclonal 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

875-886

Subventions

Organisme : NIAMS NIH HHS
ID : R01 AR074960
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM123169
Pays : United States

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Auteurs

Jianguo Wen (J)

Center for Nanoscale Materials, Argonne National Laboratory, Lemont, Illinois 60517, United States.

Shohini K Ghosh-Choudhary (SK)

School of Medicine, University of Pittsburgh, 3550 Terrace St., Pittsburgh, Pennsylvania 15213, United States.

Emily J Devereaux (EJ)

Orthopaedics Department, Emory University, Atlanta, Georgia 30322, United States.
Research Service, Atlanta VA Medical Center, Decatur, Georgia 30033, United States.

Nick J Willett (NJ)

Orthopaedics Department, Emory University, Atlanta, Georgia 30322, United States.
Research Service, Atlanta VA Medical Center, Decatur, Georgia 30033, United States.

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