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Autoregulation of thromboinflammation on biomaterial surfaces by a multicomponent therapeutic coating

Nilsson, Per H. (author)
Linnéuniversitetet,Institutionen för kemi och biomedicin (KOB),Linnaeus Ctr Biomat Chem, BMC;HoRB
N. Ekdahl, Kristina (author)
Linnéuniversitetet,Uppsala universitet,Klinisk immunologi,Institutionen för kemi och biomedicin (KOB),Uppsala University,Linnaeus Ctr Biomat Chem, BMC
Magnusson, Peetra U. (author)
Uppsala universitet,Klinisk immunologi,Uppsala University
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Qu, Hongchang (author)
University of Pennsylvania, USA
Iwata, Hiroo (author)
Kyoto University, Japan
Ricklin, Daniel (author)
University of Pennsylvania, USA
Hong, Jaan (author)
Uppsala universitet,Klinisk immunologi,Uppsala University
Lambris, John D. (author)
University of Pennsylvania, USA
Nilsson, Bo (author)
Uppsala universitet,Klinisk immunologi,Uppsala University
Teramura, Yuji (author)
Uppsala universitet,Klinisk immunologi,Uppsala University;Kyoto University, Japan
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 (creator_code:org_t)
Elsevier BV, 2013
2013
English.
In: Biomaterials. - : Elsevier BV. - 0142-9612 .- 1878-5905. ; 34:4, s. 985-994
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Activation of the thrombotic and complement systems is the main recognition and effector mechanisms in the multiple adverse biological responses triggered when biomaterials or therapeutic cells come into blood contact. We have created a surface which is auto-protective to human innate immunity by combining three fundamentally different strategies, all developed by us previously, which have been shown to induce substantial, but incomplete hemocompatibility when used separately. In summary, we have conjugated a factor H-binding peptide; and an ADP-degrading enzyme; using a PEG linker on both material and cellular surfaces. When exposed to human whole blood, factor H was specifically recruited to the modified surfaces and inhibited complement attack. In addition, activation of platelets and coagulation was efficiently attenuated, by degrading ADP. Thus, by inhibiting thromboinflammation using a multicomponent approach, we have created a hybrid surface with the potential to greatly reduce incompatibility reactions involving biomaterials and transplantation.

Subject headings

NATURVETENSKAP  -- Biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences (hsv//eng)

Keyword

Apyrase
Coagulation
Complement
Factor H-binding peptide
Poly(ethylene glycol) (PEG)
Surface modification
Autoregulations
Biological response
Biomaterial surfaces
Blood contact
Complement systems
H-binding
Hemocompatibility
Hybrid surface
Innate immunity
Modified surfaces
Multicomponents
Whole blood
Biological materials
Biomaterials
Peptides
Polyethylene glycols
Surface treatment
Surfaces
5C6 peptide
biomaterial
complement factor H
macrogol
peptide
unclassified drug
article
autoregulation
biotinylation
endothelium cell
erythrocyte
human
inflammation
multicomponent therapeutic coating
peptide synthesis
porcine aortic endothelial cell
priority journal
protein immobilization
thromboinflammation
Biomedical Sciences

Publication and Content Type

ref (subject category)
art (subject category)

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