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Expression levels of MHC class I molecules are inversely correlated with promiscuity of peptide binding

Highly polymorphic major histocompatibility complex (MHC) molecules are at the heart of adaptive immune responses, playing crucial roles in many kinds of disease and in vaccination. We report that breadth of peptide presentation and level of cell surface expression of class I molecules are inversely...

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Autores principales: Chappell, Paul E, Meziane, El Kahina, Harrison, Michael, Magiera, Łukasz, Hermann, Clemens, Mears, Laura, Wrobel, Antoni G, Durant, Charlotte, Nielsen, Lise Lotte, Buus, Søren, Ternette, Nicola, Mwangi, William, Butter, Colin, Nair, Venugopal, Ahyee, Trudy, Duggleby, Richard, Madrigal, Alejandro, Roversi, Pietro, Lea, Susan M, Kaufman, Jim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4420994/
https://www.ncbi.nlm.nih.gov/pubmed/25860507
http://dx.doi.org/10.7554/eLife.05345
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author Chappell, Paul E
Meziane, El Kahina
Harrison, Michael
Magiera, Łukasz
Hermann, Clemens
Mears, Laura
Wrobel, Antoni G
Durant, Charlotte
Nielsen, Lise Lotte
Buus, Søren
Ternette, Nicola
Mwangi, William
Butter, Colin
Nair, Venugopal
Ahyee, Trudy
Duggleby, Richard
Madrigal, Alejandro
Roversi, Pietro
Lea, Susan M
Kaufman, Jim
author_facet Chappell, Paul E
Meziane, El Kahina
Harrison, Michael
Magiera, Łukasz
Hermann, Clemens
Mears, Laura
Wrobel, Antoni G
Durant, Charlotte
Nielsen, Lise Lotte
Buus, Søren
Ternette, Nicola
Mwangi, William
Butter, Colin
Nair, Venugopal
Ahyee, Trudy
Duggleby, Richard
Madrigal, Alejandro
Roversi, Pietro
Lea, Susan M
Kaufman, Jim
author_sort Chappell, Paul E
collection PubMed
description Highly polymorphic major histocompatibility complex (MHC) molecules are at the heart of adaptive immune responses, playing crucial roles in many kinds of disease and in vaccination. We report that breadth of peptide presentation and level of cell surface expression of class I molecules are inversely correlated in both chickens and humans. This relationship correlates with protective responses against infectious pathogens including Marek's disease virus leading to lethal tumours in chickens and human immunodeficiency virus infection progressing to AIDS in humans. We propose that differences in peptide binding repertoire define two groups of MHC class I molecules strategically evolved as generalists and specialists for different modes of pathogen resistance. We suggest that differences in cell surface expression level ensure the development of optimal peripheral T cell responses. The inverse relationship of peptide repertoire and expression is evidently a fundamental property of MHC molecules, with ramifications extending beyond immunology and medicine to evolutionary biology and conservation. DOI: http://dx.doi.org/10.7554/eLife.05345.001
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spelling pubmed-44209942015-05-07 Expression levels of MHC class I molecules are inversely correlated with promiscuity of peptide binding Chappell, Paul E Meziane, El Kahina Harrison, Michael Magiera, Łukasz Hermann, Clemens Mears, Laura Wrobel, Antoni G Durant, Charlotte Nielsen, Lise Lotte Buus, Søren Ternette, Nicola Mwangi, William Butter, Colin Nair, Venugopal Ahyee, Trudy Duggleby, Richard Madrigal, Alejandro Roversi, Pietro Lea, Susan M Kaufman, Jim eLife Immunology Highly polymorphic major histocompatibility complex (MHC) molecules are at the heart of adaptive immune responses, playing crucial roles in many kinds of disease and in vaccination. We report that breadth of peptide presentation and level of cell surface expression of class I molecules are inversely correlated in both chickens and humans. This relationship correlates with protective responses against infectious pathogens including Marek's disease virus leading to lethal tumours in chickens and human immunodeficiency virus infection progressing to AIDS in humans. We propose that differences in peptide binding repertoire define two groups of MHC class I molecules strategically evolved as generalists and specialists for different modes of pathogen resistance. We suggest that differences in cell surface expression level ensure the development of optimal peripheral T cell responses. The inverse relationship of peptide repertoire and expression is evidently a fundamental property of MHC molecules, with ramifications extending beyond immunology and medicine to evolutionary biology and conservation. DOI: http://dx.doi.org/10.7554/eLife.05345.001 eLife Sciences Publications, Ltd 2015-04-10 /pmc/articles/PMC4420994/ /pubmed/25860507 http://dx.doi.org/10.7554/eLife.05345 Text en © 2015, Chappell et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Immunology
Chappell, Paul E
Meziane, El Kahina
Harrison, Michael
Magiera, Łukasz
Hermann, Clemens
Mears, Laura
Wrobel, Antoni G
Durant, Charlotte
Nielsen, Lise Lotte
Buus, Søren
Ternette, Nicola
Mwangi, William
Butter, Colin
Nair, Venugopal
Ahyee, Trudy
Duggleby, Richard
Madrigal, Alejandro
Roversi, Pietro
Lea, Susan M
Kaufman, Jim
Expression levels of MHC class I molecules are inversely correlated with promiscuity of peptide binding
title Expression levels of MHC class I molecules are inversely correlated with promiscuity of peptide binding
title_full Expression levels of MHC class I molecules are inversely correlated with promiscuity of peptide binding
title_fullStr Expression levels of MHC class I molecules are inversely correlated with promiscuity of peptide binding
title_full_unstemmed Expression levels of MHC class I molecules are inversely correlated with promiscuity of peptide binding
title_short Expression levels of MHC class I molecules are inversely correlated with promiscuity of peptide binding
title_sort expression levels of mhc class i molecules are inversely correlated with promiscuity of peptide binding
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4420994/
https://www.ncbi.nlm.nih.gov/pubmed/25860507
http://dx.doi.org/10.7554/eLife.05345
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