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Subcutaneous injection of an immunologically tolerated protein up to 5 days before skin injuries improves wound healing

Oral tolerance blocks the development of specific immune responses to proteins ingested by the oral route. One of the first registries of oral tolerance showed that guinea pigs fed corn became refractory to hypersensitivity to corn proteins. Mice fed with chow containing corn are tolerant to zein, a...

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Autores principales: Franco-Valencia, K., Nóbrega, I.B.C., Cantaruti, T., Barra, A., Klein, A., Azevedo-Jr, G.M., Costa, R.A., Carvalho, C.R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Divulgação Científica 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8851940/
https://www.ncbi.nlm.nih.gov/pubmed/35170683
http://dx.doi.org/10.1590/1414-431X2021e11735
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author Franco-Valencia, K.
Nóbrega, I.B.C.
Cantaruti, T.
Barra, A.
Klein, A.
Azevedo-Jr, G.M.
Costa, R.A.
Carvalho, C.R.
author_facet Franco-Valencia, K.
Nóbrega, I.B.C.
Cantaruti, T.
Barra, A.
Klein, A.
Azevedo-Jr, G.M.
Costa, R.A.
Carvalho, C.R.
author_sort Franco-Valencia, K.
collection PubMed
description Oral tolerance blocks the development of specific immune responses to proteins ingested by the oral route. One of the first registries of oral tolerance showed that guinea pigs fed corn became refractory to hypersensitivity to corn proteins. Mice fed with chow containing corn are tolerant to zein, and parenteral injection of zein plus adjuvant blocks immunization to unrelated proteins injected concomitantly and reduces unspecific inflammation. Extensive and prolonged inflammatory infiltrate in the wound bed is one of the causes of pathological wound healing. Previous research shows that intraperitoneal injection of zein concomitant with skin injuries reduces the inflammatory infiltrate in the wound bed and improves wound healing. Herein, we tested if one subcutaneous injection of zein before skin injury improves wound healing. We also investigated how long the effects triggered by zein could improve skin wound healing. Mice fed zein received two excisional wounds on the interscapular skin under anesthesia. Zein plus Al(OH)(3) was injected at the tail base at 10 min, or 3, 5, or 7 days before skin injuries. Wound healing was analyzed at days 7 and 40 after injury. Our results showed that a zein injection up to 5 days before skin injury reduced the inflammatory infiltrate, increased the number of T-cells in the wound bed, and improved the pattern of collagen deposition in the neodermis. These findings could promote the development of new strategies for the treatment and prevention of pathological healing using proteins normally found in the common diet.
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spelling pubmed-88519402022-02-17 Subcutaneous injection of an immunologically tolerated protein up to 5 days before skin injuries improves wound healing Franco-Valencia, K. Nóbrega, I.B.C. Cantaruti, T. Barra, A. Klein, A. Azevedo-Jr, G.M. Costa, R.A. Carvalho, C.R. Braz J Med Biol Res Research Article Oral tolerance blocks the development of specific immune responses to proteins ingested by the oral route. One of the first registries of oral tolerance showed that guinea pigs fed corn became refractory to hypersensitivity to corn proteins. Mice fed with chow containing corn are tolerant to zein, and parenteral injection of zein plus adjuvant blocks immunization to unrelated proteins injected concomitantly and reduces unspecific inflammation. Extensive and prolonged inflammatory infiltrate in the wound bed is one of the causes of pathological wound healing. Previous research shows that intraperitoneal injection of zein concomitant with skin injuries reduces the inflammatory infiltrate in the wound bed and improves wound healing. Herein, we tested if one subcutaneous injection of zein before skin injury improves wound healing. We also investigated how long the effects triggered by zein could improve skin wound healing. Mice fed zein received two excisional wounds on the interscapular skin under anesthesia. Zein plus Al(OH)(3) was injected at the tail base at 10 min, or 3, 5, or 7 days before skin injuries. Wound healing was analyzed at days 7 and 40 after injury. Our results showed that a zein injection up to 5 days before skin injury reduced the inflammatory infiltrate, increased the number of T-cells in the wound bed, and improved the pattern of collagen deposition in the neodermis. These findings could promote the development of new strategies for the treatment and prevention of pathological healing using proteins normally found in the common diet. Associação Brasileira de Divulgação Científica 2022-02-09 /pmc/articles/PMC8851940/ /pubmed/35170683 http://dx.doi.org/10.1590/1414-431X2021e11735 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Franco-Valencia, K.
Nóbrega, I.B.C.
Cantaruti, T.
Barra, A.
Klein, A.
Azevedo-Jr, G.M.
Costa, R.A.
Carvalho, C.R.
Subcutaneous injection of an immunologically tolerated protein up to 5 days before skin injuries improves wound healing
title Subcutaneous injection of an immunologically tolerated protein up to 5 days before skin injuries improves wound healing
title_full Subcutaneous injection of an immunologically tolerated protein up to 5 days before skin injuries improves wound healing
title_fullStr Subcutaneous injection of an immunologically tolerated protein up to 5 days before skin injuries improves wound healing
title_full_unstemmed Subcutaneous injection of an immunologically tolerated protein up to 5 days before skin injuries improves wound healing
title_short Subcutaneous injection of an immunologically tolerated protein up to 5 days before skin injuries improves wound healing
title_sort subcutaneous injection of an immunologically tolerated protein up to 5 days before skin injuries improves wound healing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8851940/
https://www.ncbi.nlm.nih.gov/pubmed/35170683
http://dx.doi.org/10.1590/1414-431X2021e11735
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