Cargando…

Therapeutic Efficacy of Excretory-Secretory Products of Trichinella spiralis Adult Worms on Sepsis-Induced Acute Lung Injury in a Mouse Model

Acute lung injury (ALI) is a common complication of systemic inflammation or sepsis with high morbidity and mortality. Although many studies have confirmed that helminth-derived proteins had strong immunomodulatory functions and could be used to treat inflammatory diseases, there is no report on the...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Huihui, Qiu, Dapeng, Yang, Huijuan, Yuan, Yuan, Wu, Lingqin, Chu, Liang, Zhan, Bin, Wang, Xiaoli, Sun, Yan, Xu, Wei, Yang, Xiaodi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024484/
https://www.ncbi.nlm.nih.gov/pubmed/33842398
http://dx.doi.org/10.3389/fcimb.2021.653843
_version_ 1783675319198154752
author Li, Huihui
Qiu, Dapeng
Yang, Huijuan
Yuan, Yuan
Wu, Lingqin
Chu, Liang
Zhan, Bin
Wang, Xiaoli
Sun, Yan
Xu, Wei
Yang, Xiaodi
author_facet Li, Huihui
Qiu, Dapeng
Yang, Huijuan
Yuan, Yuan
Wu, Lingqin
Chu, Liang
Zhan, Bin
Wang, Xiaoli
Sun, Yan
Xu, Wei
Yang, Xiaodi
author_sort Li, Huihui
collection PubMed
description Acute lung injury (ALI) is a common complication of systemic inflammation or sepsis with high morbidity and mortality. Although many studies have confirmed that helminth-derived proteins had strong immunomodulatory functions and could be used to treat inflammatory diseases, there is no report on the therapeutic effect of excretory-secretory products of Trichinella spiralis adult worms (Ts-AES) on sepsis-induced ALI. In this study, the therapeutic efficacy of Ts-AES on sepsis-induced ALI and the underlying immunological mechanism and the signaling pathway were investigated. The results indicated that after being treated with Ts-AES, the survival rate of mice with CLP-induced sepsis was significantly increased to 50% for 72 hours after CLP surgery compared to PBS control group with all mice died. The sepsis-induced ALI was largely mitigated characterized by reduced inflammation cell infiltration and pathological changes in lung tissue, with decreased lung injury scores and lung wet/dry weight ratio. The therapeutic efficacy of Ts-AES is associated with stimulated Tregs response with increased regulatory cytokines IL-10 and TGF-β and downregulated pro-inflammatory cytokines (TNF-α, IL-6, IL-1β). The expression of HMGB1, TLR2 and MyD88 in lung tissue was inhibited after treatment of Ts-AES. Our results demonstrated that Ts-AES play an important role in immunomodulation and confer a therapeutic effect on sepsis-induced ALI through inhibiting pro-inflammatory cytokines. The activation of Tregs and increased level of regulatory cytokines IL-10 and TGF-β are possibly involved in the immunomodulatory functions of Ts-AES through HMGB1/TLR2/MyD88 signal pathway. The findings suggest Ts-AES is a potential therapeutic agent for prevention and treatment of sepsis-induced ALI and other inflammatory diseases.
format Online
Article
Text
id pubmed-8024484
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-80244842021-04-08 Therapeutic Efficacy of Excretory-Secretory Products of Trichinella spiralis Adult Worms on Sepsis-Induced Acute Lung Injury in a Mouse Model Li, Huihui Qiu, Dapeng Yang, Huijuan Yuan, Yuan Wu, Lingqin Chu, Liang Zhan, Bin Wang, Xiaoli Sun, Yan Xu, Wei Yang, Xiaodi Front Cell Infect Microbiol Cellular and Infection Microbiology Acute lung injury (ALI) is a common complication of systemic inflammation or sepsis with high morbidity and mortality. Although many studies have confirmed that helminth-derived proteins had strong immunomodulatory functions and could be used to treat inflammatory diseases, there is no report on the therapeutic effect of excretory-secretory products of Trichinella spiralis adult worms (Ts-AES) on sepsis-induced ALI. In this study, the therapeutic efficacy of Ts-AES on sepsis-induced ALI and the underlying immunological mechanism and the signaling pathway were investigated. The results indicated that after being treated with Ts-AES, the survival rate of mice with CLP-induced sepsis was significantly increased to 50% for 72 hours after CLP surgery compared to PBS control group with all mice died. The sepsis-induced ALI was largely mitigated characterized by reduced inflammation cell infiltration and pathological changes in lung tissue, with decreased lung injury scores and lung wet/dry weight ratio. The therapeutic efficacy of Ts-AES is associated with stimulated Tregs response with increased regulatory cytokines IL-10 and TGF-β and downregulated pro-inflammatory cytokines (TNF-α, IL-6, IL-1β). The expression of HMGB1, TLR2 and MyD88 in lung tissue was inhibited after treatment of Ts-AES. Our results demonstrated that Ts-AES play an important role in immunomodulation and confer a therapeutic effect on sepsis-induced ALI through inhibiting pro-inflammatory cytokines. The activation of Tregs and increased level of regulatory cytokines IL-10 and TGF-β are possibly involved in the immunomodulatory functions of Ts-AES through HMGB1/TLR2/MyD88 signal pathway. The findings suggest Ts-AES is a potential therapeutic agent for prevention and treatment of sepsis-induced ALI and other inflammatory diseases. Frontiers Media S.A. 2021-03-24 /pmc/articles/PMC8024484/ /pubmed/33842398 http://dx.doi.org/10.3389/fcimb.2021.653843 Text en Copyright © 2021 Li, Qiu, Yang, Yuan, Wu, Chu, Zhan, Wang, Sun, Xu and Yang http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Li, Huihui
Qiu, Dapeng
Yang, Huijuan
Yuan, Yuan
Wu, Lingqin
Chu, Liang
Zhan, Bin
Wang, Xiaoli
Sun, Yan
Xu, Wei
Yang, Xiaodi
Therapeutic Efficacy of Excretory-Secretory Products of Trichinella spiralis Adult Worms on Sepsis-Induced Acute Lung Injury in a Mouse Model
title Therapeutic Efficacy of Excretory-Secretory Products of Trichinella spiralis Adult Worms on Sepsis-Induced Acute Lung Injury in a Mouse Model
title_full Therapeutic Efficacy of Excretory-Secretory Products of Trichinella spiralis Adult Worms on Sepsis-Induced Acute Lung Injury in a Mouse Model
title_fullStr Therapeutic Efficacy of Excretory-Secretory Products of Trichinella spiralis Adult Worms on Sepsis-Induced Acute Lung Injury in a Mouse Model
title_full_unstemmed Therapeutic Efficacy of Excretory-Secretory Products of Trichinella spiralis Adult Worms on Sepsis-Induced Acute Lung Injury in a Mouse Model
title_short Therapeutic Efficacy of Excretory-Secretory Products of Trichinella spiralis Adult Worms on Sepsis-Induced Acute Lung Injury in a Mouse Model
title_sort therapeutic efficacy of excretory-secretory products of trichinella spiralis adult worms on sepsis-induced acute lung injury in a mouse model
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8024484/
https://www.ncbi.nlm.nih.gov/pubmed/33842398
http://dx.doi.org/10.3389/fcimb.2021.653843
work_keys_str_mv AT lihuihui therapeuticefficacyofexcretorysecretoryproductsoftrichinellaspiralisadultwormsonsepsisinducedacutelunginjuryinamousemodel
AT qiudapeng therapeuticefficacyofexcretorysecretoryproductsoftrichinellaspiralisadultwormsonsepsisinducedacutelunginjuryinamousemodel
AT yanghuijuan therapeuticefficacyofexcretorysecretoryproductsoftrichinellaspiralisadultwormsonsepsisinducedacutelunginjuryinamousemodel
AT yuanyuan therapeuticefficacyofexcretorysecretoryproductsoftrichinellaspiralisadultwormsonsepsisinducedacutelunginjuryinamousemodel
AT wulingqin therapeuticefficacyofexcretorysecretoryproductsoftrichinellaspiralisadultwormsonsepsisinducedacutelunginjuryinamousemodel
AT chuliang therapeuticefficacyofexcretorysecretoryproductsoftrichinellaspiralisadultwormsonsepsisinducedacutelunginjuryinamousemodel
AT zhanbin therapeuticefficacyofexcretorysecretoryproductsoftrichinellaspiralisadultwormsonsepsisinducedacutelunginjuryinamousemodel
AT wangxiaoli therapeuticefficacyofexcretorysecretoryproductsoftrichinellaspiralisadultwormsonsepsisinducedacutelunginjuryinamousemodel
AT sunyan therapeuticefficacyofexcretorysecretoryproductsoftrichinellaspiralisadultwormsonsepsisinducedacutelunginjuryinamousemodel
AT xuwei therapeuticefficacyofexcretorysecretoryproductsoftrichinellaspiralisadultwormsonsepsisinducedacutelunginjuryinamousemodel
AT yangxiaodi therapeuticefficacyofexcretorysecretoryproductsoftrichinellaspiralisadultwormsonsepsisinducedacutelunginjuryinamousemodel