Topical Application of Virus-Derived Immunomodulating Proteins and Peptides to Promote Wound Healing in Mouse Models.
Administration, Cutaneous
Animals
Chitosan
/ chemistry
Cicatrix
/ genetics
Collagen Type I
/ biosynthesis
Disease Models, Animal
Drug Delivery Systems
Female
Gene Expression
Hydrogels
/ chemistry
Immunologic Factors
/ immunology
Male
Mice
Mice, Inbred C57BL
Myxoma virus
/ chemistry
Skin
/ drug effects
Surgical Wound
/ drug therapy
Viral Proteins
/ immunology
Wound Healing
/ drug effects
Full-thickness excision
Hydrogel
Viral immune modulator
Wound healing
Journal
Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969
Informations de publication
Date de publication:
2021
2021
Historique:
entrez:
27
10
2020
pubmed:
28
10
2020
medline:
27
3
2021
Statut:
ppublish
Résumé
Immune modulators play critical roles in the progression of wounds to normal or conversely delayed healing, through the regulation of normal tissue regrowth, scarring, inflammation, and growth factor expression. Many immune modulator recombinants are under active preclinical study or in clinical trial to promote improved acute or chronic wound healing and to reduce scarring. Viruses have evolved highly efficient immune modulators for the evasion of host-defensive immune responses that target and kill invasive viruses. Recent studies have proven that some of these virus-derived immune modulators can be used to promote wound healing with significantly improved speed and reduced scarring in rodent models. Mouse full-thickness excisional wound model is one of the most commonly used animal models used to study wound healing for its similarity to humans in the healing phases and associated cellular and molecular mechanisms. This chapter introduces this mouse dermal wound healing model in detail for application in studying viral immune modulators as new treatments to promote wound healing. Details of hydrogel, protein construction, and topical application methods for these therapeutic proteins are provided in this chapter.
Identifiants
pubmed: 33108665
doi: 10.1007/978-1-0716-1012-1_12
doi:
Substances chimiques
Collagen Type I
0
Hydrogels
0
Immunologic Factors
0
Viral Proteins
0
Chitosan
9012-76-4
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM