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Monoclonal antibody 2C5 specifically targets neutrophil extracellular traps.
Mendes, Livia P; Rostamizadeh, Kobra; Gollomp, Kandace; Myerson, Jacob W; Marcos-Contreras, Oscar A; Zamora, Marco; Luther, Ed; Brenner, Jacob S; Filipczak, Nina; Li, Xiang; Torchilin, Vladimir P.
Afiliação
  • Mendes LP; Center for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University , Boston, MA, USA.
  • Rostamizadeh K; Zanjan Pharmaceutical Nanotechnology Research Center, School of Pharmacy, Pharmaceutical Biomaterials Department, Zanjan University of Medical Sciences , Zanjan, Iran.
  • Gollomp K; Division of Hematology, Children's Hospital of Philadelphia , Philadelphia, PA, USA.
  • Myerson JW; Department of Systems Pharmacology and Translational Therapeutics, University of Philadelphia , Philadelphia, PA, USA.
  • Marcos-Contreras OA; Department of Systems Pharmacology and Translational Therapeutics, University of Philadelphia , Philadelphia, PA, USA.
  • Zamora M; Department of Systems Pharmacology and Translational Therapeutics, University of Philadelphia , Philadelphia, PA, USA.
  • Luther E; Department of Pharmaceutical Sciences, Northeastern University , Boston, MA, USA.
  • Brenner JS; Department of Systems Pharmacology and Translational Therapeutics, University of Philadelphia , Philadelphia, PA, USA.
  • Filipczak N; Pulmonary, Allergy, & Critical Care Division, University of Philadelphia , PA, USA.
  • Li X; Center for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University , Boston, MA, USA.
  • Torchilin VP; Center for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University , Boston, MA, USA.
MAbs ; 12(1): 1850394, 2020.
Article em En | MEDLINE | ID: mdl-33323006
ABSTRACT
Neutrophils can release DNA and granular cytoplasmic proteins that form smooth filaments of stacked nucleosomes (NS). These structures, called neutrophil extracellular traps (NETs), are involved in multiple pathological processes, and NET formation and removal are clinically significant. The monoclonal antibody 2C5 has strong specificity toward intact NS but not to individual NS components, indicating that 2C5 could potentially target NS in NETs. In this study, NETs were generated in vitro using neutrophils and HL-60 cells differentiated into granulocyte-like cells. The specificity of 2C5 toward NETs was evaluated by ELISA, which showed that it binds to NETs with the specificity similar to that for purified nucleohistone substrate. Immunofluorescence showed that 2C5 stains NETs in both static and perfused microfluidic cell cultures, even after NET compaction. Modification of liposomes with 2C5 dramatically enhanced liposome association with NETs. Our results suggest that 2C5 could be used to identify and visualize NETs and serve as a ligand for NET-targeted diagnostics and therapies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anticorpos Monoclonais Murinos / Armadilhas Extracelulares / Especificidade de Anticorpos Limite: Animals / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anticorpos Monoclonais Murinos / Armadilhas Extracelulares / Especificidade de Anticorpos Limite: Animals / Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article