Nanometer- and angstrom-scale characteristics that modulate complement responses to nanoparticles

Research output: Contribution to journalJournal articleResearchpeer-review

Documents

  • Fulltext

    Final published version, 6.3 MB, PDF document

  • S. Moein Moghimi
  • Hajira B. Haroon
  • Yaghmur, Anan
  • Dmitri Simberg
  • Panagiotis N. Trohopoulos

The contribution of the complement system to non-specific host defence and maintenance of homeostasis is well appreciated. Many particulate systems trigger complement activation but the underlying mechanisms are still poorly understood. Activation of the complement cascade could lead to particle opsonisation by the cleavage products of the third complement protein and might promote inflammatory reactions. Antibody binding in a controlled manner and/or sensing of particles by the complement pattern-recognition molecules such as C1q and mannose-binding lectin can trigger complement activation. Particle curvature and spacing arrangement/periodicity of surface functional groups/ligands are two important parameters that modulate complement responses through multivalent engagement with and conformational regulation of surface-bound antibodies and complement pattern-recognition molecules. Thus, a better fundamental understanding of nanometer- and angstrom-scale parameters that modulate particle interaction with antibodies and complement proteins could portend new possibilities for engineering of particulate drug carriers and biomedical platforms with tuneable complement responses and is discussed here.

Original languageEnglish
JournalJournal of Controlled Release
Volume351
Pages (from-to)432-443
ISSN0168-3659
DOIs
Publication statusPublished - 2022

Bibliographical note

Funding Information:
S.M.M. acknowledges support by the European Union's Horizon 2020 programme funded under H2020-EU.1.3. – Excellent Science – Marie Sklodowska-Curie Actions, grant agreement ID. 956544 (DIRNANO: Directing the immune response through designed nanomaterials). H.B.H. is an Early Stage Researcher supported by the DIRNANO programme. A.Y. & S.M.M. acknowledge support by the Danish Council for Independent Research – Technology and Production Sciences; reference DFF-7017-00065. P.N.T. & S.M.M. acknowledge support by the European Union's Seventh Framework Programme (FP7-NMP-2012-Large-6) under the grant agreement no. 310337 (CosmoPHOS-nano Large-Scale Project). D.S. acknowledges support by the National Institute of Health grant R01AI154959.

Funding Information:
S.M.M. acknowledges support by the European Union's Horizon 2020 programme funded under H2020-EU.1.3 . – Excellent Science – Marie Sklodowska-Curie Actions , grant agreement ID. 956544 (DIRNANO: Directing the immune response through designed nanomaterials). H.B.H. is an Early Stage Researcher supported by the DIRNANO programme. A.Y. & S.M.M. acknowledge support by the Danish Council for Independent Research – Technology and Production Sciences ; reference DFF-7017-00065 . P.N.T. & S.M.M. acknowledge support by the European Union's Seventh Framework Programme (FP7-NMP-2012-Large-6) under the grant agreement no. 310337 (CosmoPHOS-nano Large-Scale Project). D.S. acknowledges support by the National Institute of Health grant R01AI154959 .

Publisher Copyright:
© 2022 The Authors

    Research areas

  • Antibodies, C1q, Complement system, Dendrimers, Factor H, Mannose-binding lectin, Nanoparticles

Number of downloads are based on statistics from Google Scholar and www.ku.dk


No data available

ID: 321274652