PolySialic Acid Nanoparticles Actuate Complement-Factor-H-Mediated Inhibition of the Alternative Complement Pathway: A Safer Potential Therapy for Age-Related Macular Degeneration.

alternative pathway disease geographic atrophy glycobiology immune system inflammation macrophages microglia ophthalmology treatment

Journal

Pharmaceuticals (Basel, Switzerland)
ISSN: 1424-8247
Titre abrégé: Pharmaceuticals (Basel)
Pays: Switzerland
ID NLM: 101238453

Informations de publication

Date de publication:
17 Apr 2024
Historique:
received: 06 03 2024
revised: 10 04 2024
accepted: 11 04 2024
medline: 27 4 2024
pubmed: 27 4 2024
entrez: 27 4 2024
Statut: epublish

Résumé

The alternative pathway of the complement system is implicated in the etiology of age-related macular degeneration (AMD). Complement depletion with pegcetacoplan and avacincaptad pegol are FDA-approved treatments for geographic atrophy in AMD that, while effective, have clinically observed risks of choroidal neovascular (CNV) conversion, optic neuritis, and retinal vasculitis, leaving room for other equally efficacious but safer therapeutics, including Poly Sialic acid (PSA) nanoparticle (PolySia-NP)-actuated complement factor H (CFH) alternative pathway inhibition. Our previous paper demonstrated that PolySia-NP inhibits pro-inflammatory polarization and cytokine release. Here, we extend these findings by investigating the therapeutic potential of PolySia-NP to attenuate the alternative complement pathway. First, we show that PolySia-NP binds CFH and enhances affinity to C3b. Next, we demonstrate that PolySia-NP treatment of human serum suppresses alternative pathway hemolytic activity and C3b deposition. Further, we show that treating human macrophages with PolySia-NP is non-toxic and reduces markers of complement activity. Finally, we describe PolySia-NP-treatment-induced decreases in neovascularization and inflammatory response in a laser-induced CNV mouse model of neovascular AMD. In conclusion, PolySia-NP suppresses alternative pathway complement activity in human serum, human macrophage, and mouse CNV without increasing neovascularization.

Identifiants

pubmed: 38675477
pii: ph17040517
doi: 10.3390/ph17040517
pii:
doi:

Types de publication

Journal Article

Langues

eng

Auteurs

Sheri L Peterson (SL)

Aviceda Therapeutics Inc., Cambridge, MA 02142, USA.

Anitha Krishnan (A)

Aviceda Therapeutics Inc., Cambridge, MA 02142, USA.

Diyan Patel (D)

Aviceda Therapeutics Inc., Cambridge, MA 02142, USA.

Ali Khanehzar (A)

Aviceda Therapeutics Inc., Cambridge, MA 02142, USA.

Amit Lad (A)

Aviceda Therapeutics Inc., Cambridge, MA 02142, USA.

Jutamas Shaughnessy (J)

Division of Infectious Diseases and Immunology, University of Massachusetts Chan Medical School, Worcester, MA 01655, USA.

Sanjay Ram (S)

Division of Infectious Diseases and Immunology, University of Massachusetts Chan Medical School, Worcester, MA 01655, USA.

David Callanan (D)

Aviceda Therapeutics Inc., Cambridge, MA 02142, USA.
Department of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

Derek Kunimoto (D)

Aviceda Therapeutics Inc., Cambridge, MA 02142, USA.

Mohamed A Genead (MA)

Aviceda Therapeutics Inc., Cambridge, MA 02142, USA.

Michael J Tolentino (MJ)

Aviceda Therapeutics Inc., Cambridge, MA 02142, USA.
Department of Ophthalmology, University of Central Florida School of Medicine, Orlando, FL 32827, USA.
Department of Ophthalmology, Orlando College of Osteopathic Medicine, Orlando, FL 34787, USA.

Classifications MeSH