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GrpE Immunization Protects Against Ureaplasma urealyticum Infection in BALB/C Mice

Nucleotide exchange factor (GrpE), a highly conserved antigen, is rapidly expressed and upregulated when Ureaplasma urealyticum infects a host, which could act as a candidative vaccine if it can induce an anti-U. urealyticum immune reaction. Here, we evaluated the vaccine potential of recombinant Gr...

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Autores principales: Tang, Yanhong, Guo, Fangyi, Lei, Aihua, Xiang, Jing, Liu, Pengqin, Ten, Wenyou, Dai, Guozhi, Li, Ranhui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7411329/
https://www.ncbi.nlm.nih.gov/pubmed/32849509
http://dx.doi.org/10.3389/fimmu.2020.01495
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author Tang, Yanhong
Guo, Fangyi
Lei, Aihua
Xiang, Jing
Liu, Pengqin
Ten, Wenyou
Dai, Guozhi
Li, Ranhui
author_facet Tang, Yanhong
Guo, Fangyi
Lei, Aihua
Xiang, Jing
Liu, Pengqin
Ten, Wenyou
Dai, Guozhi
Li, Ranhui
author_sort Tang, Yanhong
collection PubMed
description Nucleotide exchange factor (GrpE), a highly conserved antigen, is rapidly expressed and upregulated when Ureaplasma urealyticum infects a host, which could act as a candidative vaccine if it can induce an anti-U. urealyticum immune reaction. Here, we evaluated the vaccine potential of recombinant GrpE protein adjuvanted by Freund's adjuvant (FA), to protect against U. urealyticum genital tract infection in a mouse model. After booster immunization in mice with FA, the GrpE can induced both humoral and cellular immune response after intramuscular injection into BALB/c mice. A strong humoral immune response was detected in the GrpE-immunized mice characterized by production of high titers of antigen-specific serum IgG (IgG1, IgG2a, and IgG3) antibodies. At the same time, the GrpE also induced a Th1-biased cytokine spectrum with high levels of IFN-γ and TNF-α after re-stimulation with immunogen GrpE in vitro, suggesting that GrpE could trigger the Th1 response when used for vaccination in the presence of FA. Although GrpE vaccination in the presence of a Th1-type adjuvant-induced had readily detectable Th1 responses, there wasn't increase inflammation in response to the infection. More importantly, the robust immune responses in mice after immunization with GrpE showed a significantly reduced U. urealyticum burden in cervical tissues. Histopathological analysis confirmed that tissues of GrpE-immunized BALB/c mice were protected against the pathological effects of U. urealyticum infection. In conclusion, this study preliminarily reveals GrpE protein as a promising new candidate vaccine for preventing U. urealyticum reproductive tract infection.
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spelling pubmed-74113292020-08-25 GrpE Immunization Protects Against Ureaplasma urealyticum Infection in BALB/C Mice Tang, Yanhong Guo, Fangyi Lei, Aihua Xiang, Jing Liu, Pengqin Ten, Wenyou Dai, Guozhi Li, Ranhui Front Immunol Immunology Nucleotide exchange factor (GrpE), a highly conserved antigen, is rapidly expressed and upregulated when Ureaplasma urealyticum infects a host, which could act as a candidative vaccine if it can induce an anti-U. urealyticum immune reaction. Here, we evaluated the vaccine potential of recombinant GrpE protein adjuvanted by Freund's adjuvant (FA), to protect against U. urealyticum genital tract infection in a mouse model. After booster immunization in mice with FA, the GrpE can induced both humoral and cellular immune response after intramuscular injection into BALB/c mice. A strong humoral immune response was detected in the GrpE-immunized mice characterized by production of high titers of antigen-specific serum IgG (IgG1, IgG2a, and IgG3) antibodies. At the same time, the GrpE also induced a Th1-biased cytokine spectrum with high levels of IFN-γ and TNF-α after re-stimulation with immunogen GrpE in vitro, suggesting that GrpE could trigger the Th1 response when used for vaccination in the presence of FA. Although GrpE vaccination in the presence of a Th1-type adjuvant-induced had readily detectable Th1 responses, there wasn't increase inflammation in response to the infection. More importantly, the robust immune responses in mice after immunization with GrpE showed a significantly reduced U. urealyticum burden in cervical tissues. Histopathological analysis confirmed that tissues of GrpE-immunized BALB/c mice were protected against the pathological effects of U. urealyticum infection. In conclusion, this study preliminarily reveals GrpE protein as a promising new candidate vaccine for preventing U. urealyticum reproductive tract infection. Frontiers Media S.A. 2020-07-31 /pmc/articles/PMC7411329/ /pubmed/32849509 http://dx.doi.org/10.3389/fimmu.2020.01495 Text en Copyright © 2020 Tang, Guo, Lei, Xiang, Liu, Ten, Dai and Li. 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 Immunology
Tang, Yanhong
Guo, Fangyi
Lei, Aihua
Xiang, Jing
Liu, Pengqin
Ten, Wenyou
Dai, Guozhi
Li, Ranhui
GrpE Immunization Protects Against Ureaplasma urealyticum Infection in BALB/C Mice
title GrpE Immunization Protects Against Ureaplasma urealyticum Infection in BALB/C Mice
title_full GrpE Immunization Protects Against Ureaplasma urealyticum Infection in BALB/C Mice
title_fullStr GrpE Immunization Protects Against Ureaplasma urealyticum Infection in BALB/C Mice
title_full_unstemmed GrpE Immunization Protects Against Ureaplasma urealyticum Infection in BALB/C Mice
title_short GrpE Immunization Protects Against Ureaplasma urealyticum Infection in BALB/C Mice
title_sort grpe immunization protects against ureaplasma urealyticum infection in balb/c mice
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7411329/
https://www.ncbi.nlm.nih.gov/pubmed/32849509
http://dx.doi.org/10.3389/fimmu.2020.01495
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