Implications of endotoxins in wound healing: a narrative review

被引:30
作者
Rippon, Mark G. [1 ]
Westgate, Samantha [2 ]
Rogers, Alan A.
机构
[1] Univ Huddersfield, Huddersfield, W Yorkshire, England
[2] Perfectus Biomed Grp, Cheshire, England
关键词
antimicrobials; bacterial pathogens; endotoxins; endotoxin-binding wound dressings; wound; wound bed; wound care; wound dressing; wound healing; TOLL-LIKE RECEPTORS; BACTERIAL-ENDOTOXIN; POLYMYXIN-B; RELEASE; LPS; DRESSINGS; BIOFILM; LIPOPOLYSACCHARIDE; SEPSIS; MODEL;
D O I
10.12968/jowc.2022.31.5.380
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Bacterial toxins are thought to play a role in delayed wound healing in critically colonised and infected wounds. Endotoxins are released from Gram-negative bacteria when they are lysed by host phagocytic cells during an immune response, or by antimicrobial agents, potentially leading to a detrimental effect on the host tissues. Endotoxins can affect all aspects of the wound healing process, leading to delayed healing and contributing to wound chronicity. Release of endotoxins by bacteria can also have serious systemic effects (for example, septic shock) that can lead to high levels of patient mortality. This review summarises the role and implications on wound healing of bacterial endotoxins, describing the impact of endotoxins on the various phases of the wound healing response. There is a paucity of in vivo/clinical evidence linking endotoxins attributed to a wound (via antibiotic treatment) or their release from infecting bacteria with parameters of delayed wound healing. Future work should investigate if this link is apparent and determine the mechanism(s) by which such detrimental effects occur, offering an opportunity to identify possible treatment pathways. This paper describes the phenomenon of antimicrobialinduced endotoxin release and summarises the use of wound dressings to reduce wound bioburden without inducing microbial death and subsequent release of endotoxins, thus limiting their detrimental effects. Declaration of interest: This work was funded by Essity. The authors have no other conflicts of interest to declare.
引用
收藏
页码:380 / 392
页数:12
相关论文
共 145 条
[41]   Polymyxin Delivery Systems: Recent Advances and Challenges [J].
Dubashynskaya, Natallia V. ;
Skorik, Yury A. .
PHARMACEUTICALS, 2020, 13 (05)
[42]   Topical antimicrobial agents for treating foot ulcers in people with diabetes [J].
Dumville, Jo C. ;
Lipsky, Benjamin A. ;
Hoey, Christopher ;
Cruciani, Mario ;
Fiscon, Marta ;
Xia, Jun .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2017, (06)
[43]   Immunology of Wound Healing [J].
Ellis S. ;
Lin E.J. ;
Tartar D. .
Current Dermatology Reports, 2018, 7 (4) :350-358
[44]   Innate immunity and coagulation [J].
Esmon, C. T. ;
Xu, J. ;
Lupu, F. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2011, 9 :182-188
[45]   Immunomodulation in Sepsis: The Role of Endotoxin Removal by Polymyxin B-Immobilized Cartridge [J].
Esteban, Elisabeth ;
Ferrer, Ricard ;
Alsina, Laia ;
Artigas, Antonio .
MEDIATORS OF INFLAMMATION, 2013, 2013
[46]  
Farhana A., 2021, StatPearls
[47]   Primed PMNs in healthy mouse and human circulation are first responders during acute inflammation [J].
Fine, Noah ;
Barzilay, Oriyah ;
Sun, Chunxiang ;
Wellappuli, Nimali ;
Tanwir, Farzeen ;
Chadwick, Jeffrey W. ;
Oveisi, Morvarid ;
Tasevski, Nikola ;
Prescott, David ;
Gargan, Martin ;
Philpott, Dana J. ;
Dror, Yigal ;
Glogauer, Michael .
BLOOD ADVANCES, 2019, 3 (10) :1622-1637
[48]   Animal models of sepsis [J].
Fink, Mitchell P. .
VIRULENCE, 2014, 5 (01) :143-153
[49]   The biofilm matrix [J].
Flemming, Hans-Curt ;
Wingender, Jost .
NATURE REVIEWS MICROBIOLOGY, 2010, 8 (09) :623-633
[50]   Metabolic endotoxemia and diabetes mellitus: A systematic review [J].
Geraldo Gomes, Junia Maria ;
Costa, Jorge de Assis ;
Goncalues Alfenas, Rita de Cassia .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2017, 68 :133-144