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Immunomodulatory effects of Rhipicephalus haemaphysaloides serpin RHS2 on host immune responses

BACKGROUND: Rhipicephalus haemaphysaloides is a widespread tick species in China and other South East Asian countries, where it is the vector of many pathogens. The objective of this study was to study the role of serpin (serine protease inhibitor) during the tick-host interaction. METHODS: The diff...

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Autores principales: Xu, Zhengmao, Lin, Zhibing, Wei, Nana, Di, Qing, Cao, Jie, Zhou, Yongzhi, Gong, Haiyan, Zhang, Houshuang, Zhou, Jinlin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624921/
https://www.ncbi.nlm.nih.gov/pubmed/31296257
http://dx.doi.org/10.1186/s13071-019-3607-4
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author Xu, Zhengmao
Lin, Zhibing
Wei, Nana
Di, Qing
Cao, Jie
Zhou, Yongzhi
Gong, Haiyan
Zhang, Houshuang
Zhou, Jinlin
author_facet Xu, Zhengmao
Lin, Zhibing
Wei, Nana
Di, Qing
Cao, Jie
Zhou, Yongzhi
Gong, Haiyan
Zhang, Houshuang
Zhou, Jinlin
author_sort Xu, Zhengmao
collection PubMed
description BACKGROUND: Rhipicephalus haemaphysaloides is a widespread tick species in China and other South East Asian countries, where it is the vector of many pathogens. The objective of this study was to study the role of serpin (serine protease inhibitor) during the tick-host interaction. METHODS: The differentiation of bone marrow-derived dendritic cells (BMDC) was induced in vitro, and the effect of RHS2 on the maturation of DCs was evaluated. The effects of RHS2 on T cell activation and cytotoxic T lymphocytes’ (CTLs) activity were analyzed by flow cytometry. Antibody subtypes after immunization of mice with RHS2 and OVA were determined. RESULTS: RHS2 can inhibit the differentiation of bone marrow-derived cells into DCs and promote their differentiation into macrophages. RHS2 can inhibit the maturation of DCs and the expression of CD80, CD86 and MHCII. The number of CD3(+)CD4(+) and CD3(+)CD8(+) T cells secreting IFN-γ, IL-2 and TNF-α was decreased, and the number of CD3(+)CD4(+) T cells secreting IL-4 was increased, indicating that RHS2 can inhibit the activation of CD4 T cells and CD8 T cells, leading to inhibition of Th1 immune response. RHS2 inhibits the elimination of target cells by cytotoxic T lymphocytes. After immunization of mice with RHS2 and OVA, serum IgG2b was significantly reduced and IgM was increased. CONCLUSIONS: The results show that RHS2 has an inhibitory effect on the host immune response. Ticks have evolved various ways to circumvent adaptive immunity. Their serpin inhibits BMDC differentiation to reduce immune responses.
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spelling pubmed-66249212019-07-23 Immunomodulatory effects of Rhipicephalus haemaphysaloides serpin RHS2 on host immune responses Xu, Zhengmao Lin, Zhibing Wei, Nana Di, Qing Cao, Jie Zhou, Yongzhi Gong, Haiyan Zhang, Houshuang Zhou, Jinlin Parasit Vectors Research BACKGROUND: Rhipicephalus haemaphysaloides is a widespread tick species in China and other South East Asian countries, where it is the vector of many pathogens. The objective of this study was to study the role of serpin (serine protease inhibitor) during the tick-host interaction. METHODS: The differentiation of bone marrow-derived dendritic cells (BMDC) was induced in vitro, and the effect of RHS2 on the maturation of DCs was evaluated. The effects of RHS2 on T cell activation and cytotoxic T lymphocytes’ (CTLs) activity were analyzed by flow cytometry. Antibody subtypes after immunization of mice with RHS2 and OVA were determined. RESULTS: RHS2 can inhibit the differentiation of bone marrow-derived cells into DCs and promote their differentiation into macrophages. RHS2 can inhibit the maturation of DCs and the expression of CD80, CD86 and MHCII. The number of CD3(+)CD4(+) and CD3(+)CD8(+) T cells secreting IFN-γ, IL-2 and TNF-α was decreased, and the number of CD3(+)CD4(+) T cells secreting IL-4 was increased, indicating that RHS2 can inhibit the activation of CD4 T cells and CD8 T cells, leading to inhibition of Th1 immune response. RHS2 inhibits the elimination of target cells by cytotoxic T lymphocytes. After immunization of mice with RHS2 and OVA, serum IgG2b was significantly reduced and IgM was increased. CONCLUSIONS: The results show that RHS2 has an inhibitory effect on the host immune response. Ticks have evolved various ways to circumvent adaptive immunity. Their serpin inhibits BMDC differentiation to reduce immune responses. BioMed Central 2019-07-11 /pmc/articles/PMC6624921/ /pubmed/31296257 http://dx.doi.org/10.1186/s13071-019-3607-4 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
Xu, Zhengmao
Lin, Zhibing
Wei, Nana
Di, Qing
Cao, Jie
Zhou, Yongzhi
Gong, Haiyan
Zhang, Houshuang
Zhou, Jinlin
Immunomodulatory effects of Rhipicephalus haemaphysaloides serpin RHS2 on host immune responses
title Immunomodulatory effects of Rhipicephalus haemaphysaloides serpin RHS2 on host immune responses
title_full Immunomodulatory effects of Rhipicephalus haemaphysaloides serpin RHS2 on host immune responses
title_fullStr Immunomodulatory effects of Rhipicephalus haemaphysaloides serpin RHS2 on host immune responses
title_full_unstemmed Immunomodulatory effects of Rhipicephalus haemaphysaloides serpin RHS2 on host immune responses
title_short Immunomodulatory effects of Rhipicephalus haemaphysaloides serpin RHS2 on host immune responses
title_sort immunomodulatory effects of rhipicephalus haemaphysaloides serpin rhs2 on host immune responses
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6624921/
https://www.ncbi.nlm.nih.gov/pubmed/31296257
http://dx.doi.org/10.1186/s13071-019-3607-4
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