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Innate immunity activation on biomaterial surfaces: A mechanistic model and coping strategies

Journal

ADVANCED DRUG DELIVERY REVIEWS
Volume 63, Issue 12, Pages 1042-1050

Publisher

ELSEVIER
DOI: 10.1016/j.addr.2011.06.012

Keywords

Autoprotection; Biomaterial; Coagulation; Complement; Contact activation; Inflammation; Innate immunity

Funding

  1. Swedish Research Council (VR) [2009-4675, 2009-4462]
  2. Swedish Research Council
  3. Swedish Research Council/SSF/Vinnova [60761701]
  4. U.S. National Institutes of Health [AI068730, AI030040, AI072106, EB3968, GM062134]
  5. Linnaeus University

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When an artificial biomaterial (e.g., a stent or implantable pump) is exposed to blood, plasma proteins immediately adhere to the surface, creating a new interface between the biomaterial and the blood. The recognition proteins within the complement and contact activation/coagulation cascade systems of the blood will be bound to, or inserted into, this protein film and generate different mediators that will activate polymorphonuclear leukocytes and monocytes, as well as platelets. Under clinical conditions, the ultimate outcome of these processes may be thrombotic and inflammatory reactions, and consequently the composition and conformation of the proteins in the initial layer formed on the surface will to a large extent determine the outcome of a treatment involving the biomaterial, affecting both the functionality of the material and the patient's life quality. This review presents models of biomaterial-induced activation processes and describes various strategies to attenuate potential adverse reactions by conjugating bioactive molecules to surfaces or by introducing nanostructures. (C) 2011 Elsevier B.V. All rights reserved.

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