The Lectin Pathway of Complement and Biocompatibility

Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

In modern health technologies the use of biomaterials in the form of stents, haemodialysis tubes, artificial implants, bypass circuits etc. is rapidly expanding. The exposure of synthetic, foreign surfaces to the blood and tissue of the host, calls for strict biocompatibility in respect to contact activation, the coagulation system and the complement system. The complement system is an important part of the initial immune response and consists of fluid phase molecules in the blood stream. Three different activation pathways can initiate the complement system, the lectin, the classical and the alternative pathway, all converging in an amplification loop of the cascade system and downstream reactions. Thus, when exposed to foreign substances complement components will be activated and lead to a powerful inflammatory response. Biosurface induced complement activation is a recognised issue that has been broadly documented. However, the specific role of lectin pathway and the pattern recognition molecules initiating the pathway has only been transiently investigated. Here we review the current data on the field.

Original languageEnglish
Title of host publicationImmune Responses to Biosurfaces : Mechanisms and Therapeutic Interventions
Number of pages16
Volume865
PublisherSpringer
Publication date2015
Pages77-92
Chapter5
ISBN (Print)978-3-319-18602-3
ISBN (Electronic)978-3-319-18603-0
DOIs
Publication statusPublished - 2015
SeriesAdvances in Experimental Medicine and Biology
ISSN0065-2598

    Research areas

  • Biocompatible Materials, Blood Coagulation, Blood Coagulation Factors, Collectins, Complement Activation, Complement Pathway, Mannose-Binding Lectin, Extracorporeal Circulation, Gene Expression Regulation, Humans, Lectins, Mannose-Binding Protein-Associated Serine Proteases, Protein Binding, Receptors, Pattern Recognition, Signal Transduction, Surface Properties

ID: 162872200