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Heat shock proteins 70 and 90 from Clonorchis sinensis induce Th1 response and stimulate antibody production

BACKGROUND: Heat shock proteins (HSPs) are found in all prokaryotes and most compartments of eukaryotic cells. Members of the HSP family mediate immune responses to tissue damage or cellular stress. However, little is known about the immune response induced by the oriental liver fluke, Clonorchis si...

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Autores principales: Chung, Eun Joo, Jeong, Young-Il, Lee, Myoung-Ro, Kim, Yu Jung, Lee, Sang-Eun, Cho, Shin-Hyeong, Lee, Won-Ja, Park, Mi-Yeoun, Ju, Jung-Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333430/
https://www.ncbi.nlm.nih.gov/pubmed/28249599
http://dx.doi.org/10.1186/s13071-017-2026-7
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author Chung, Eun Joo
Jeong, Young-Il
Lee, Myoung-Ro
Kim, Yu Jung
Lee, Sang-Eun
Cho, Shin-Hyeong
Lee, Won-Ja
Park, Mi-Yeoun
Ju, Jung-Won
author_facet Chung, Eun Joo
Jeong, Young-Il
Lee, Myoung-Ro
Kim, Yu Jung
Lee, Sang-Eun
Cho, Shin-Hyeong
Lee, Won-Ja
Park, Mi-Yeoun
Ju, Jung-Won
author_sort Chung, Eun Joo
collection PubMed
description BACKGROUND: Heat shock proteins (HSPs) are found in all prokaryotes and most compartments of eukaryotic cells. Members of the HSP family mediate immune responses to tissue damage or cellular stress. However, little is known about the immune response induced by the oriental liver fluke, Clonorchis sinensis, even though this organism is carcinogenic to humans. We address this issue in the present study in mouse bone marrow dendritic cells (mBMDCs), using recombinant HSP70 and 90 from C. sinensis (rCsHSP70 and rCsHSP90). METHODS: rCsHSP70 and rCsHSP90 were produced in an E. coli system. Purified recombinant proteins were treated in BMDCs isolated from C57BL/6 mice. T cells were isolated from Balb/c mice and co-cultured with activated mBMDCs. Expression of surface molecules was measured by flow cytometry and cytokine secretion was quantified using ELISA. C57BL/6 mice were divided into four groups, including peptide alone, peptide/Freund’s adjuvant, peptide/CsHSP70, peptide/CsHSP90, and were immunized intraperitoneally three times. Two weeks after final immunization, antibodies against peptide were measured using ELISA. RESULTS: Both proteins induced a dose-dependent upregulation in major histocompatibility complex and co-stimulatory molecule expression and increased secretion of pro-inflammatory cytokines including interleukin (IL)-1β, -6, and -12p70 and tumor necrosis factor-α in mBMDCs. Furthermore, when allogenic T cells were incubated with mBMDCs activated by rCsHSP70 and rCsHSP90, the helper T cell (Th)1 cytokine interferon-γ was up-regulated whereas the level of the Th2 cytokine IL-4 was unchanged. These results indicate that rCsHSPs predominantly induce a Th1 response. Over and above these results, we also demonstrated that the production of peptide-specific antibodies can be activated after immunization via in vitro peptide binding with rCsHSP70 or rCsHSP90. CONCLUSION: This study showed for the first time that the HSP or HSP/peptide complexes of C. sinensis could be considered as a more effective vaccine against C. sinensis infection as results of the activator of host immune response as well as the adjuvant for antigenic peptide conjugate to induce peptide-specific antibody response in mice.
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spelling pubmed-53334302017-03-06 Heat shock proteins 70 and 90 from Clonorchis sinensis induce Th1 response and stimulate antibody production Chung, Eun Joo Jeong, Young-Il Lee, Myoung-Ro Kim, Yu Jung Lee, Sang-Eun Cho, Shin-Hyeong Lee, Won-Ja Park, Mi-Yeoun Ju, Jung-Won Parasit Vectors Research BACKGROUND: Heat shock proteins (HSPs) are found in all prokaryotes and most compartments of eukaryotic cells. Members of the HSP family mediate immune responses to tissue damage or cellular stress. However, little is known about the immune response induced by the oriental liver fluke, Clonorchis sinensis, even though this organism is carcinogenic to humans. We address this issue in the present study in mouse bone marrow dendritic cells (mBMDCs), using recombinant HSP70 and 90 from C. sinensis (rCsHSP70 and rCsHSP90). METHODS: rCsHSP70 and rCsHSP90 were produced in an E. coli system. Purified recombinant proteins were treated in BMDCs isolated from C57BL/6 mice. T cells were isolated from Balb/c mice and co-cultured with activated mBMDCs. Expression of surface molecules was measured by flow cytometry and cytokine secretion was quantified using ELISA. C57BL/6 mice were divided into four groups, including peptide alone, peptide/Freund’s adjuvant, peptide/CsHSP70, peptide/CsHSP90, and were immunized intraperitoneally three times. Two weeks after final immunization, antibodies against peptide were measured using ELISA. RESULTS: Both proteins induced a dose-dependent upregulation in major histocompatibility complex and co-stimulatory molecule expression and increased secretion of pro-inflammatory cytokines including interleukin (IL)-1β, -6, and -12p70 and tumor necrosis factor-α in mBMDCs. Furthermore, when allogenic T cells were incubated with mBMDCs activated by rCsHSP70 and rCsHSP90, the helper T cell (Th)1 cytokine interferon-γ was up-regulated whereas the level of the Th2 cytokine IL-4 was unchanged. These results indicate that rCsHSPs predominantly induce a Th1 response. Over and above these results, we also demonstrated that the production of peptide-specific antibodies can be activated after immunization via in vitro peptide binding with rCsHSP70 or rCsHSP90. CONCLUSION: This study showed for the first time that the HSP or HSP/peptide complexes of C. sinensis could be considered as a more effective vaccine against C. sinensis infection as results of the activator of host immune response as well as the adjuvant for antigenic peptide conjugate to induce peptide-specific antibody response in mice. BioMed Central 2017-03-01 /pmc/articles/PMC5333430/ /pubmed/28249599 http://dx.doi.org/10.1186/s13071-017-2026-7 Text en © The Author(s). 2017 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
Chung, Eun Joo
Jeong, Young-Il
Lee, Myoung-Ro
Kim, Yu Jung
Lee, Sang-Eun
Cho, Shin-Hyeong
Lee, Won-Ja
Park, Mi-Yeoun
Ju, Jung-Won
Heat shock proteins 70 and 90 from Clonorchis sinensis induce Th1 response and stimulate antibody production
title Heat shock proteins 70 and 90 from Clonorchis sinensis induce Th1 response and stimulate antibody production
title_full Heat shock proteins 70 and 90 from Clonorchis sinensis induce Th1 response and stimulate antibody production
title_fullStr Heat shock proteins 70 and 90 from Clonorchis sinensis induce Th1 response and stimulate antibody production
title_full_unstemmed Heat shock proteins 70 and 90 from Clonorchis sinensis induce Th1 response and stimulate antibody production
title_short Heat shock proteins 70 and 90 from Clonorchis sinensis induce Th1 response and stimulate antibody production
title_sort heat shock proteins 70 and 90 from clonorchis sinensis induce th1 response and stimulate antibody production
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333430/
https://www.ncbi.nlm.nih.gov/pubmed/28249599
http://dx.doi.org/10.1186/s13071-017-2026-7
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