Surface Geometry of Cargo-less Gold Nanoparticles Is a Driving Force for Selective Targeting of Activated Neutrophils to Reduce Thrombosis in Antiphospholipid Syndrome.


Journal

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

Informations de publication

Date de publication:
08 11 2023
Historique:
medline: 9 11 2023
pubmed: 27 10 2023
entrez: 26 10 2023
Statut: ppublish

Résumé

Antiphospholipid syndrome (APS) is an autoimmune disease characterized by recurrent arterial, venous, and microvascular thrombosis where activated neutrophils play a determinant role. However, neutrophils are challenging to target given their short lifespan in circulation and spontaneous activation. Screening of a small library of gold nanoparticles (AuNPs) led to the discovery of a formulation capable of targeting activated neutrophil attachment and has demonstrated that star-shaped, anti-PSGL-1-antibody-coated AuNPs (aPSGL-1-AuNPs) were more efficacious compared with other shapes of AuNPs. Our findings further revealed an exciting and safe targeting mode toward activated neutrophils in the APS mouse model induced by human-patient-derived antiphospholipid IgGs. Our studies demonstrate that targeting is dependent on the specific topographical features of the highly segregated PSGL-1 on the activated neutrophil surface for which a high affinity shape-driven nanomedicine can be designed and implemented. As such, star-shaped aPSGL-1-AuNPs serve as a promising nanoimmunotherapy for immunothrombosis associated with neutrophil adhesion in APS.

Identifiants

pubmed: 37884274
doi: 10.1021/acs.nanolett.3c02075
pmc: PMC10636870
doi:

Substances chimiques

Gold 7440-57-5
Immunoglobulin G 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

9690-9696

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL130516
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL155450
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL142647
Pays : United States

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Auteurs

Lin Di (L)

Department of Biomedical Engineering, Case Western Reserve University School of Engineering, Cleveland, Ohio 44106, United States.
Cardiovascular Research Institute, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106, United States.

Asha Thomas (A)

Cardiovascular Research Institute, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106, United States.
Division of Hematology and Oncology, University Hospitals Cleveland Medical Center, Cleveland, Ohio 44106, United States.

Lauren Switala (L)

Department of Biomedical Engineering, Case Western Reserve University School of Engineering, Cleveland, Ohio 44106, United States.
Cardiovascular Research Institute, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106, United States.

Kenneth Kalikasingh (K)

Cardiovascular Research Institute, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106, United States.
Division of Hematology and Oncology, University Hospitals Cleveland Medical Center, Cleveland, Ohio 44106, United States.

Stephanie Lapping (S)

Cardiovascular Research Institute, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106, United States.
Division of Hematology and Oncology, University Hospitals Cleveland Medical Center, Cleveland, Ohio 44106, United States.

Lalitha Nayak (L)

Cardiovascular Research Institute, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106, United States.
Division of Hematology and Oncology, University Hospitals Cleveland Medical Center, Cleveland, Ohio 44106, United States.

Andrei Maiseyeu (A)

Department of Biomedical Engineering, Case Western Reserve University School of Engineering, Cleveland, Ohio 44106, United States.
Cardiovascular Research Institute, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106, United States.

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