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The proportion, origin and pro-inflammation roles of low density neutrophils in SFTS disease
BACKGROUND: Severe fever with thrombocytopenia syndrome (SFTS) is a novel emerging viral infectious disease. We explored the percentage, origins and functional roles of low density neutrophils (LDNs), one of the neutrophils subsets, in SFTS. METHODS: The LDNs and normal density neutrophils (NDNs) fr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6360754/ https://www.ncbi.nlm.nih.gov/pubmed/30717709 http://dx.doi.org/10.1186/s12879-019-3701-4 |
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author | Li, Yajiao Li, Huiyu Wang, Hua Pan, Hong Zhao, Huixia Jin, Honglin Jie, Shenghua |
author_facet | Li, Yajiao Li, Huiyu Wang, Hua Pan, Hong Zhao, Huixia Jin, Honglin Jie, Shenghua |
author_sort | Li, Yajiao |
collection | PubMed |
description | BACKGROUND: Severe fever with thrombocytopenia syndrome (SFTS) is a novel emerging viral infectious disease. We explored the percentage, origins and functional roles of low density neutrophils (LDNs), one of the neutrophils subsets, in SFTS. METHODS: The LDNs and normal density neutrophils (NDNs) from blood of SFTS and normal volunteers which were collected separately. The percentage, origins and the phagocytic capability of SFTS viral (SFTSV) of LDNs were investigated by flow cytometry and real time PCR. The capacity of LDNs to secrete cytokines and to damage endothelial cells was assessed by ELISA and flow cytometry. RESULTS: We observed that the proportion of LDNs increased dramatically compared with the healthy donors and became the dominant circulating neutrophil population in SFTS patients. Interestingly, the NDNs from the normal donors could switch to LDNs under the SFTS environment. Moreover, SFTSV load in LDNs was significantly higher than that of NDNs in the severe SFTS patients. In addition, the LDNs secreted much higher levels of pro-inflammatory cytokines than NDNs in SFTS and could induce endothelial cell injury. CONCLUSION: The NDNs can be converted to LDNs. This conversion mechanism could become the source of LDNs. The LDNs in severe SFTS patient could engulf more SFTSV and exhibit pro-inflammation functions. TRIAL REGISTRATION: The Ethics Committee of Tongji Medical College, Huazhong University of Science and Technology (IORG No: IORG0003571) gave a final APPROVAL for the study. |
format | Online Article Text |
id | pubmed-6360754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63607542019-02-08 The proportion, origin and pro-inflammation roles of low density neutrophils in SFTS disease Li, Yajiao Li, Huiyu Wang, Hua Pan, Hong Zhao, Huixia Jin, Honglin Jie, Shenghua BMC Infect Dis Research Article BACKGROUND: Severe fever with thrombocytopenia syndrome (SFTS) is a novel emerging viral infectious disease. We explored the percentage, origins and functional roles of low density neutrophils (LDNs), one of the neutrophils subsets, in SFTS. METHODS: The LDNs and normal density neutrophils (NDNs) from blood of SFTS and normal volunteers which were collected separately. The percentage, origins and the phagocytic capability of SFTS viral (SFTSV) of LDNs were investigated by flow cytometry and real time PCR. The capacity of LDNs to secrete cytokines and to damage endothelial cells was assessed by ELISA and flow cytometry. RESULTS: We observed that the proportion of LDNs increased dramatically compared with the healthy donors and became the dominant circulating neutrophil population in SFTS patients. Interestingly, the NDNs from the normal donors could switch to LDNs under the SFTS environment. Moreover, SFTSV load in LDNs was significantly higher than that of NDNs in the severe SFTS patients. In addition, the LDNs secreted much higher levels of pro-inflammatory cytokines than NDNs in SFTS and could induce endothelial cell injury. CONCLUSION: The NDNs can be converted to LDNs. This conversion mechanism could become the source of LDNs. The LDNs in severe SFTS patient could engulf more SFTSV and exhibit pro-inflammation functions. TRIAL REGISTRATION: The Ethics Committee of Tongji Medical College, Huazhong University of Science and Technology (IORG No: IORG0003571) gave a final APPROVAL for the study. BioMed Central 2019-02-04 /pmc/articles/PMC6360754/ /pubmed/30717709 http://dx.doi.org/10.1186/s12879-019-3701-4 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Li, Yajiao Li, Huiyu Wang, Hua Pan, Hong Zhao, Huixia Jin, Honglin Jie, Shenghua The proportion, origin and pro-inflammation roles of low density neutrophils in SFTS disease |
title | The proportion, origin and pro-inflammation roles of low density neutrophils in SFTS disease |
title_full | The proportion, origin and pro-inflammation roles of low density neutrophils in SFTS disease |
title_fullStr | The proportion, origin and pro-inflammation roles of low density neutrophils in SFTS disease |
title_full_unstemmed | The proportion, origin and pro-inflammation roles of low density neutrophils in SFTS disease |
title_short | The proportion, origin and pro-inflammation roles of low density neutrophils in SFTS disease |
title_sort | proportion, origin and pro-inflammation roles of low density neutrophils in sfts disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6360754/ https://www.ncbi.nlm.nih.gov/pubmed/30717709 http://dx.doi.org/10.1186/s12879-019-3701-4 |
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