A shift of paradigm: From avoiding nanoparticular complement activation in the field of nanomedicines to its exploitation in the context of vaccine development.

Antigen presentation Antigen uptake CARPA Complement Complement activation Complement regulation Lymph node targeting Nanoparticles Nanoparticluar vaccines Nanotherapeutics Vaccine development

Journal

European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V
ISSN: 1873-3441
Titre abrégé: Eur J Pharm Biopharm
Pays: Netherlands
ID NLM: 9109778

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 27 07 2023
revised: 01 10 2023
accepted: 10 10 2023
medline: 11 12 2023
pubmed: 15 10 2023
entrez: 14 10 2023
Statut: ppublish

Résumé

The complement system plays a central role in our innate immunity to fight pathogenic microorganisms, foreign and altered cells, or any modified molecule. Consequences of complement activation include cell lysis, release of histamines, and opsonization of foreign structures in preparation for phagocytosis. Because nanoparticles interact with the immune system in various ways and can massively activate the complement system due to their virus-mimetic size and foreign texture, detrimental side effects have been described after administration like pro-inflammatory responses, inflammation, mild to severe anaphylactic crisis and potentially complement activated-related pseudoallergy (CARPA). Therefore, application of nanotherapeutics has sometimes been observed with restraint, and avoiding or even suppressing complement activation has been of utmost priority. In contrast, in the field of vaccine development, particularly protein-based immunogens that are attached to the surface of nanoparticles, may profit from complement activation regarding breadth and potency of immune response. Improved transport to the regional lymph nodes, enhanced antigen uptake and presentation, as well as beneficial effects on immune cells like B-, T- and follicular dendritic cells may be exploited by strategic nanoparticle design aimed to activate the complement system. However, a shift of paradigm regarding complement activation by nanoparticular vaccines can only be achieved if these beneficial effects are accurately elicited and overshooting effects avoided.

Identifiants

pubmed: 37838145
pii: S0939-6411(23)00268-0
doi: 10.1016/j.ejpb.2023.10.008
pii:
doi:

Substances chimiques

Complement System Proteins 9007-36-7
Antigens 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

119-128

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Clara Barbey (C)

Department of Pharmaceutical Technology, University Regensburg, Regensburg, Germany.

Hannah Wolf (H)

Department of Experimental Ophthalmology, University Marburg, Marburg, Germany.

Ralf Wagner (R)

Institute of Medical Microbiology and Hygiene, University of Regensburg, Regensburg, Germany; Institute of Clinical Microbiology and Hygiene, University Hospital Regensburg, Regensburg, Germany.

Diana Pauly (D)

Department of Experimental Ophthalmology, University Marburg, Marburg, Germany.

Miriam Breunig (M)

Department of Pharmaceutical Technology, University Regensburg, Regensburg, Germany. Electronic address: miriam.breunig@ur.de.

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Classifications MeSH