MHC-I-restricted epitopes conserved among variola and other related orthopoxviruses are recognized by T cells 30 years after vaccination

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Standard

MHC-I-restricted epitopes conserved among variola and other related orthopoxviruses are recognized by T cells 30 years after vaccination. / Tang, S T; Wang, M; Lamberth, K; Harndahl, M; Dziegiel, M H; Claesson, M H; Buus, S; Lund, Ole.

I: Archives of Virology, Bind 153, Nr. 10, 2008, s. 1833-44.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Tang, ST, Wang, M, Lamberth, K, Harndahl, M, Dziegiel, MH, Claesson, MH, Buus, S & Lund, O 2008, 'MHC-I-restricted epitopes conserved among variola and other related orthopoxviruses are recognized by T cells 30 years after vaccination', Archives of Virology, bind 153, nr. 10, s. 1833-44. https://doi.org/10.1007/s00705-008-0194-7

APA

Tang, S. T., Wang, M., Lamberth, K., Harndahl, M., Dziegiel, M. H., Claesson, M. H., Buus, S., & Lund, O. (2008). MHC-I-restricted epitopes conserved among variola and other related orthopoxviruses are recognized by T cells 30 years after vaccination. Archives of Virology, 153(10), 1833-44. https://doi.org/10.1007/s00705-008-0194-7

Vancouver

Tang ST, Wang M, Lamberth K, Harndahl M, Dziegiel MH, Claesson MH o.a. MHC-I-restricted epitopes conserved among variola and other related orthopoxviruses are recognized by T cells 30 years after vaccination. Archives of Virology. 2008;153(10):1833-44. https://doi.org/10.1007/s00705-008-0194-7

Author

Tang, S T ; Wang, M ; Lamberth, K ; Harndahl, M ; Dziegiel, M H ; Claesson, M H ; Buus, S ; Lund, Ole. / MHC-I-restricted epitopes conserved among variola and other related orthopoxviruses are recognized by T cells 30 years after vaccination. I: Archives of Virology. 2008 ; Bind 153, Nr. 10. s. 1833-44.

Bibtex

@article{31cc2130e31611ddb5fc000ea68e967b,
title = "MHC-I-restricted epitopes conserved among variola and other related orthopoxviruses are recognized by T cells 30 years after vaccination",
abstract = "It is many years since the general population has been vaccinated against smallpox virus. Here, we report that human leukocyte antigen (HLA) class I restricted T cell epitopes can be recognized more than 30 years after vaccination. Using bioinformatic methods, we predicted 177 potential cytotoxic T lymphocyte epitopes. Eight epitopes were confirmed to stimulate IFN-gamma release by T cells in smallpox-vaccinated subjects. The epitopes were restricted by five supertypes (HLA-A1, -A2, -A24 -A26 and -B44). Significant T cell responses were detected against 8 of 45 peptides with an HLA class I affinity of K(D) less than or equal to 5 nM, whereas no T cell responses were detected against 60 peptides with an HLA affinity of K(D) more than 5 nM. All epitopes were fully conserved in seven variola, vaccinia and cowpox strains. Knowledge of the long-term response to smallpox vaccination may lead to a better understanding of poxvirus immunity and may aid in the development of new improved vaccines and diagnostic tools.",
author = "Tang, {S T} and M Wang and K Lamberth and M Harndahl and Dziegiel, {M H} and Claesson, {M H} and S Buus and Ole Lund",
note = "Keywords: Adult; Aged; Animals; Epitopes, T-Lymphocyte; Female; Histocompatibility Antigens Class I; Humans; Interferon-gamma; Male; Middle Aged; Orthopoxvirus; Smallpox Vaccine; T-Lymphocytes, Cytotoxic; Time Factors",
year = "2008",
doi = "10.1007/s00705-008-0194-7",
language = "English",
volume = "153",
pages = "1833--44",
journal = "Archiv fur die gesamte Virusforschung",
issn = "0304-8608",
publisher = "Springer Wien",
number = "10",

}

RIS

TY - JOUR

T1 - MHC-I-restricted epitopes conserved among variola and other related orthopoxviruses are recognized by T cells 30 years after vaccination

AU - Tang, S T

AU - Wang, M

AU - Lamberth, K

AU - Harndahl, M

AU - Dziegiel, M H

AU - Claesson, M H

AU - Buus, S

AU - Lund, Ole

N1 - Keywords: Adult; Aged; Animals; Epitopes, T-Lymphocyte; Female; Histocompatibility Antigens Class I; Humans; Interferon-gamma; Male; Middle Aged; Orthopoxvirus; Smallpox Vaccine; T-Lymphocytes, Cytotoxic; Time Factors

PY - 2008

Y1 - 2008

N2 - It is many years since the general population has been vaccinated against smallpox virus. Here, we report that human leukocyte antigen (HLA) class I restricted T cell epitopes can be recognized more than 30 years after vaccination. Using bioinformatic methods, we predicted 177 potential cytotoxic T lymphocyte epitopes. Eight epitopes were confirmed to stimulate IFN-gamma release by T cells in smallpox-vaccinated subjects. The epitopes were restricted by five supertypes (HLA-A1, -A2, -A24 -A26 and -B44). Significant T cell responses were detected against 8 of 45 peptides with an HLA class I affinity of K(D) less than or equal to 5 nM, whereas no T cell responses were detected against 60 peptides with an HLA affinity of K(D) more than 5 nM. All epitopes were fully conserved in seven variola, vaccinia and cowpox strains. Knowledge of the long-term response to smallpox vaccination may lead to a better understanding of poxvirus immunity and may aid in the development of new improved vaccines and diagnostic tools.

AB - It is many years since the general population has been vaccinated against smallpox virus. Here, we report that human leukocyte antigen (HLA) class I restricted T cell epitopes can be recognized more than 30 years after vaccination. Using bioinformatic methods, we predicted 177 potential cytotoxic T lymphocyte epitopes. Eight epitopes were confirmed to stimulate IFN-gamma release by T cells in smallpox-vaccinated subjects. The epitopes were restricted by five supertypes (HLA-A1, -A2, -A24 -A26 and -B44). Significant T cell responses were detected against 8 of 45 peptides with an HLA class I affinity of K(D) less than or equal to 5 nM, whereas no T cell responses were detected against 60 peptides with an HLA affinity of K(D) more than 5 nM. All epitopes were fully conserved in seven variola, vaccinia and cowpox strains. Knowledge of the long-term response to smallpox vaccination may lead to a better understanding of poxvirus immunity and may aid in the development of new improved vaccines and diagnostic tools.

U2 - 10.1007/s00705-008-0194-7

DO - 10.1007/s00705-008-0194-7

M3 - Journal article

C2 - 18797815

VL - 153

SP - 1833

EP - 1844

JO - Archiv fur die gesamte Virusforschung

JF - Archiv fur die gesamte Virusforschung

SN - 0304-8608

IS - 10

ER -

ID: 9749438