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The cross-reactivity of the enterovirus 71 to human brain tissue and identification of the cross-reactivity related fragments

BACKGROUND: EV71 occasionally cause a series of severe neurological symptoms, including aseptic meningitis, encephalitis, and poliomyelitis-like paralysis. However, the neurological destruction mechanism was remained to be clarified. This study described the cross reaction between EV71 induced IgG a...

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Autores principales: Jia, Chun Shi, Liu, Jiang Ning, Li, Wan Bo, Ma, Chun Mei, Lin, Shu Zhu, Hao, Yi, Gao, Xue Zhong, Liu, Xiao Lin, Xu, Yan Feng, Zhang, Lian Feng, Qin, Chuan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2839975/
https://www.ncbi.nlm.nih.gov/pubmed/20170551
http://dx.doi.org/10.1186/1743-422X-7-47
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author Jia, Chun Shi
Liu, Jiang Ning
Li, Wan Bo
Ma, Chun Mei
Lin, Shu Zhu
Hao, Yi
Gao, Xue Zhong
Liu, Xiao Lin
Xu, Yan Feng
Zhang, Lian Feng
Qin, Chuan
author_facet Jia, Chun Shi
Liu, Jiang Ning
Li, Wan Bo
Ma, Chun Mei
Lin, Shu Zhu
Hao, Yi
Gao, Xue Zhong
Liu, Xiao Lin
Xu, Yan Feng
Zhang, Lian Feng
Qin, Chuan
author_sort Jia, Chun Shi
collection PubMed
description BACKGROUND: EV71 occasionally cause a series of severe neurological symptoms, including aseptic meningitis, encephalitis, and poliomyelitis-like paralysis. However, the neurological destruction mechanism was remained to be clarified. This study described the cross reaction between EV71 induced IgG and human brain tissue. RESULTS: Cross reaction of the IgG from 30 EV71 infected patients' sera to human tissues of cerebra was observed, which suggested that some EV71 antigens could induce IgG cross-reactivity to human cerebra. To identify the regions of EV71 virus that containing above antigens, the polypeptide of virus was divided into 19 peptides by expression in prokaryotes cell. Mouse anti-sera of these peptides was prepared and applied in immunohistochemical staining with human adult and fetus brain tissue, respectively. The result indicated the 19 peptides can be classified into three groups: strong cross-reactivity, weak cross-reactivity and no cross-reactivity with human brain tissue according the cross reaction activity. Then, the increased Blood Brain Barrier (BBB) permeability and permits IgG entry in neonatal mice after EV71 infection was determined. CONCLUSION: EV71 induced IgG could enter BBB and cross-reacted with brain tissue in EV71 infected neonatal mice, and then the peptides of EV71 that could induce cross-reactivity with brain tissue were identified, which should be avoided in future vaccine designing.
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spelling pubmed-28399752010-03-17 The cross-reactivity of the enterovirus 71 to human brain tissue and identification of the cross-reactivity related fragments Jia, Chun Shi Liu, Jiang Ning Li, Wan Bo Ma, Chun Mei Lin, Shu Zhu Hao, Yi Gao, Xue Zhong Liu, Xiao Lin Xu, Yan Feng Zhang, Lian Feng Qin, Chuan Virol J Research BACKGROUND: EV71 occasionally cause a series of severe neurological symptoms, including aseptic meningitis, encephalitis, and poliomyelitis-like paralysis. However, the neurological destruction mechanism was remained to be clarified. This study described the cross reaction between EV71 induced IgG and human brain tissue. RESULTS: Cross reaction of the IgG from 30 EV71 infected patients' sera to human tissues of cerebra was observed, which suggested that some EV71 antigens could induce IgG cross-reactivity to human cerebra. To identify the regions of EV71 virus that containing above antigens, the polypeptide of virus was divided into 19 peptides by expression in prokaryotes cell. Mouse anti-sera of these peptides was prepared and applied in immunohistochemical staining with human adult and fetus brain tissue, respectively. The result indicated the 19 peptides can be classified into three groups: strong cross-reactivity, weak cross-reactivity and no cross-reactivity with human brain tissue according the cross reaction activity. Then, the increased Blood Brain Barrier (BBB) permeability and permits IgG entry in neonatal mice after EV71 infection was determined. CONCLUSION: EV71 induced IgG could enter BBB and cross-reacted with brain tissue in EV71 infected neonatal mice, and then the peptides of EV71 that could induce cross-reactivity with brain tissue were identified, which should be avoided in future vaccine designing. BioMed Central 2010-02-22 /pmc/articles/PMC2839975/ /pubmed/20170551 http://dx.doi.org/10.1186/1743-422X-7-47 Text en Copyright ©2010 Jia et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Jia, Chun Shi
Liu, Jiang Ning
Li, Wan Bo
Ma, Chun Mei
Lin, Shu Zhu
Hao, Yi
Gao, Xue Zhong
Liu, Xiao Lin
Xu, Yan Feng
Zhang, Lian Feng
Qin, Chuan
The cross-reactivity of the enterovirus 71 to human brain tissue and identification of the cross-reactivity related fragments
title The cross-reactivity of the enterovirus 71 to human brain tissue and identification of the cross-reactivity related fragments
title_full The cross-reactivity of the enterovirus 71 to human brain tissue and identification of the cross-reactivity related fragments
title_fullStr The cross-reactivity of the enterovirus 71 to human brain tissue and identification of the cross-reactivity related fragments
title_full_unstemmed The cross-reactivity of the enterovirus 71 to human brain tissue and identification of the cross-reactivity related fragments
title_short The cross-reactivity of the enterovirus 71 to human brain tissue and identification of the cross-reactivity related fragments
title_sort cross-reactivity of the enterovirus 71 to human brain tissue and identification of the cross-reactivity related fragments
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2839975/
https://www.ncbi.nlm.nih.gov/pubmed/20170551
http://dx.doi.org/10.1186/1743-422X-7-47
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