The influence of a biofilm-dispersing wound gel on the wound healing process

被引:4
作者
Bounds, Kayla [1 ,2 ]
Colmer-Hamood, Jane A. [2 ,3 ]
Myntti, Matthew [4 ]
Jeter, Randall M. [1 ]
Hamood, Abdul N. [2 ,5 ]
机构
[1] Texas Tech Univ, Dept Biol Sci, Lubbock, TX 79409 USA
[2] Texas Tech Univ, Hlth Sci Ctr, Dept Immunol & Mol Microbiol, 3601 4th St,STOP 6591, Lubbock, TX 79430 USA
[3] Texas Tech Univ, Hlth Sci Ctr, Dept Med Educ, Lubbock, TX 79430 USA
[4] Next Sci LLC, Res & Dev, Jacksonville, FL USA
[5] Texas Tech Univ, Hlth Sci Ctr, Dept Surg, Lubbock, TX 79430 USA
关键词
cellular infiltration; cytokines; novel wound therapy; wound closure; wound healing; NATURAL-KILLER-CELLS; MATRIX METALLOPROTEINASES; GROWTH-FACTORS; PEG HYDROGELS; REPAIR; ANGIOGENESIS; INFILTRATION; REGENERATION; INFLAMMATION; NEUTROPHILS;
D O I
10.1111/iwj.13653
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Topical antimicrobials that reduce the bacterial bioburden within a chronically-infected wound may have helpful or harmful effects on the healing process. We used murine models of full-thickness skin wounds to determine the effects of the novel biofilm-dispersing wound gel (BDWG) and its gel base on the healing of uninfected wounds. The rate of wound closure over 19 days was comparable among the BDWG-treated (BT) wounds and the controls. Compared with the controls, histology of the BT wounds showed formation of a stable blood clot at day 1, more neovascularisation and reepithelialisation at day 3, and more organised healing at day 7. Fluorescence-activated cell sorting analysis showed a lower percentage of neutrophils in wounded tissues of the BT group at days 1 and 3, and significantly more M2 macrophages at day 3. Levels of proinflammatory cytokines and chemokines were increased over the uninjured baseline within the wounds of all treatment groups but the levels were significantly lower in the BT group at day 1, modulating the inflammatory response. Our results suggest that BDWG does not interfere with the wound healing process and may enhance it by lowering inflammation and allowing transition to the proliferative stage of wound healing by day 3.
引用
收藏
页码:553 / 572
页数:20
相关论文
共 67 条
[1]  
Attinger C.E, 2006, PLAST RECONSTR SURG, V117
[2]   Growth factors and cytokines in wound healing [J].
Barrientos, Stephan ;
Stojadinovic, Olivera ;
Golinko, Michael S. ;
Brem, Harold ;
Tomic-Canic, Marjana .
WOUND REPAIR AND REGENERATION, 2008, 16 (05) :585-601
[3]   Skewed distribution of natural killer cells in psoriasis skin lesions [J].
Batista, Mariana D. ;
Ho, Emily L. ;
Kuebler, Peter J. ;
Milush, Jeffrey M. ;
Lanier, Lewis L. ;
Kallas, Esper G. ;
York, Vanessa A. ;
Chang, David ;
Liao, Wilson ;
Unemori, Patrick ;
Leslie, Kieron S. ;
Maurer, Toby ;
Nixon, Douglas F. .
EXPERIMENTAL DERMATOLOGY, 2013, 22 (01) :64-66
[4]  
Baum CL, 2005, DERMATOL SURG, V31, P674
[5]   Reduced Neutrophil Chemotaxis and Infiltration Contributes to Delayed Resolution of Cutaneous Wound Infection with Advanced Age [J].
Brubaker, Aleah L. ;
Rendon, Juan L. ;
Ramirez, Luis ;
Choudhry, Mashkoor A. ;
Kovacs, Elizabeth J. .
JOURNAL OF IMMUNOLOGY, 2013, 190 (04) :1746-1757
[6]   Superabsorbent crosslinked carboxymethyl cellulose-PEG hydrogels for potential wound dressing applications [J].
Capanema, Nadia S. V. ;
Mansur, Alexandra A. P. ;
de Jesus, Anderson C. ;
Carvalho, Sandhra M. ;
de Oliveira, Luiz C. ;
Mansur, Herman S. .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2018, 106 :1218-1234
[7]  
Cardiff Robert D, 2014, Cold Spring Harb Protoc, V2014, P655, DOI 10.1101/pdb.prot073411
[8]  
Castrogiovanni P, 2010, WOUNDS, V22, P256
[9]  
Cerqueira MT, 2014, TISSUE ENG PT A, V20, P1369, DOI [10.1089/ten.tea.2013.0460, 10.1089/ten.TEA.2013.0460]
[10]   Tumour-vasculature development via endothelial-to-mesenchymal transition after radiotherapy controls CD44v6+ cancer cell and macrophage polarization [J].
Choi, Seo-Hyun ;
Kim, A-Ram ;
Nam, Jae-Kyung ;
Kim, Jin-Mo ;
Kim, Jee-Youn ;
Seo, Haeng Ran ;
Lee, Hae-June ;
Cho, Jaeho ;
Lee, Yoon-Jin .
NATURE COMMUNICATIONS, 2018, 9