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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |