Induction of immune gene expression and inflammatory mediator release by commonly used surgical suture materials: an experimental in vitro study

Abstract Background Surgeons have a range of materials to choose from to complete wound closure, yet surprisingly very little is still known about the body’s immune response to the suture materials in current use. The growing literature of adverse suture material reactions provided the objective of...

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Main Authors: Alistair M. Lock, Ryan Gao, Dorit Naot, Brendan Coleman, Jillian Cornish, David S. Musson
Format: Article
Language:English
Published: BMC 2017-05-01
Series:Patient Safety in Surgery
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13037-017-0132-2
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spelling doaj-79b14fd6d47647949232aad36c4a63182020-11-25T00:41:11ZengBMCPatient Safety in Surgery1754-94932017-05-011111810.1186/s13037-017-0132-2Induction of immune gene expression and inflammatory mediator release by commonly used surgical suture materials: an experimental in vitro studyAlistair M. Lock0Ryan Gao1Dorit Naot2Brendan Coleman3Jillian Cornish4David S. Musson5Department of Medicine, University of AucklandDepartment of Medicine, University of AucklandDepartment of Medicine, University of AucklandDepartment of Orthopaedics, Middlemore HospitalDepartment of Medicine, University of AucklandDepartment of Medicine, University of AucklandAbstract Background Surgeons have a range of materials to choose from to complete wound closure, yet surprisingly very little is still known about the body’s immune response to the suture materials in current use. The growing literature of adverse suture material reactions provided the objective of this study, to use in vitro assays to quantify levels of inflammation produced by seven commonly used suture materials in surgical procedures. Methods Human monocyte/macrophage THP-1 cells were exposed to suture materials for 1, 3 and 5 days. Gene expression and protein secretion of six inflammatory cytokines and two cell surface markers were assessed using qPCR and ELISA respectively, with LPS exposure providing a positive control. Furthermore, a IL-1β/IL-1RA marker ratio was assessed to determine the balance between pro-/anti-inflammatory expression. Results The findings from our in vitro study suggest that four commonly used suture materials cause upregulation of pro-inflammatory markers indicative of an early foreign body reaction, with no balance from anti-inflammatory markers. Conclusions As prolonged early pro-inflammation is known to produce delayed wound healing responses, the knowledge produced from this study has potential to improve informed surgical decision making and patient safety. This work has the capability to reduce suture-related adverse immune reactions, and therefore positively affect patient outcomes.http://link.springer.com/article/10.1186/s13037-017-0132-2In vitroImmune responseSuture materialsWound closure
collection DOAJ
language English
format Article
sources DOAJ
author Alistair M. Lock
Ryan Gao
Dorit Naot
Brendan Coleman
Jillian Cornish
David S. Musson
spellingShingle Alistair M. Lock
Ryan Gao
Dorit Naot
Brendan Coleman
Jillian Cornish
David S. Musson
Induction of immune gene expression and inflammatory mediator release by commonly used surgical suture materials: an experimental in vitro study
Patient Safety in Surgery
In vitro
Immune response
Suture materials
Wound closure
author_facet Alistair M. Lock
Ryan Gao
Dorit Naot
Brendan Coleman
Jillian Cornish
David S. Musson
author_sort Alistair M. Lock
title Induction of immune gene expression and inflammatory mediator release by commonly used surgical suture materials: an experimental in vitro study
title_short Induction of immune gene expression and inflammatory mediator release by commonly used surgical suture materials: an experimental in vitro study
title_full Induction of immune gene expression and inflammatory mediator release by commonly used surgical suture materials: an experimental in vitro study
title_fullStr Induction of immune gene expression and inflammatory mediator release by commonly used surgical suture materials: an experimental in vitro study
title_full_unstemmed Induction of immune gene expression and inflammatory mediator release by commonly used surgical suture materials: an experimental in vitro study
title_sort induction of immune gene expression and inflammatory mediator release by commonly used surgical suture materials: an experimental in vitro study
publisher BMC
series Patient Safety in Surgery
issn 1754-9493
publishDate 2017-05-01
description Abstract Background Surgeons have a range of materials to choose from to complete wound closure, yet surprisingly very little is still known about the body’s immune response to the suture materials in current use. The growing literature of adverse suture material reactions provided the objective of this study, to use in vitro assays to quantify levels of inflammation produced by seven commonly used suture materials in surgical procedures. Methods Human monocyte/macrophage THP-1 cells were exposed to suture materials for 1, 3 and 5 days. Gene expression and protein secretion of six inflammatory cytokines and two cell surface markers were assessed using qPCR and ELISA respectively, with LPS exposure providing a positive control. Furthermore, a IL-1β/IL-1RA marker ratio was assessed to determine the balance between pro-/anti-inflammatory expression. Results The findings from our in vitro study suggest that four commonly used suture materials cause upregulation of pro-inflammatory markers indicative of an early foreign body reaction, with no balance from anti-inflammatory markers. Conclusions As prolonged early pro-inflammation is known to produce delayed wound healing responses, the knowledge produced from this study has potential to improve informed surgical decision making and patient safety. This work has the capability to reduce suture-related adverse immune reactions, and therefore positively affect patient outcomes.
topic In vitro
Immune response
Suture materials
Wound closure
url http://link.springer.com/article/10.1186/s13037-017-0132-2
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