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Classification of Human Leukocyte Antigen (HLA) Supertypes

Identification of new antigenic peptides, derived from infectious agents or cancer cells, which bind to human leukocyte antigen (HLA) class I and II molecules, is of importance for the development of new effective vaccines capable of activating the cellular arm of the immune response. However, the b...

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Detalles Bibliográficos
Autores principales: Wang, Mingjun, Claesson, Mogens H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7121184/
https://www.ncbi.nlm.nih.gov/pubmed/25048132
http://dx.doi.org/10.1007/978-1-4939-1115-8_17
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author Wang, Mingjun
Claesson, Mogens H.
author_facet Wang, Mingjun
Claesson, Mogens H.
author_sort Wang, Mingjun
collection PubMed
description Identification of new antigenic peptides, derived from infectious agents or cancer cells, which bind to human leukocyte antigen (HLA) class I and II molecules, is of importance for the development of new effective vaccines capable of activating the cellular arm of the immune response. However, the barrier to the development of peptide-based vaccines with maximum population coverage is that the restricting HLA genes are extremely polymorphic resulting in a vast diversity of peptide-binding HLA specificities and a low population coverage for any given peptide–HLA specificity. One way to reduce this complexity is to group thousands of different HLA molecules into several so-called HLA supertypes: a classification that refers to a group of HLA alleles with largely overlapping peptide binding specificities. In this chapter, we focus on the state-of-the-art classification of HLA supertypes including HLA-I supertypes and HLA-II supertypes and their application in development of peptide-based vaccines.
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spelling pubmed-71211842020-04-06 Classification of Human Leukocyte Antigen (HLA) Supertypes Wang, Mingjun Claesson, Mogens H. Immunoinformatics Article Identification of new antigenic peptides, derived from infectious agents or cancer cells, which bind to human leukocyte antigen (HLA) class I and II molecules, is of importance for the development of new effective vaccines capable of activating the cellular arm of the immune response. However, the barrier to the development of peptide-based vaccines with maximum population coverage is that the restricting HLA genes are extremely polymorphic resulting in a vast diversity of peptide-binding HLA specificities and a low population coverage for any given peptide–HLA specificity. One way to reduce this complexity is to group thousands of different HLA molecules into several so-called HLA supertypes: a classification that refers to a group of HLA alleles with largely overlapping peptide binding specificities. In this chapter, we focus on the state-of-the-art classification of HLA supertypes including HLA-I supertypes and HLA-II supertypes and their application in development of peptide-based vaccines. 2014-05-06 /pmc/articles/PMC7121184/ /pubmed/25048132 http://dx.doi.org/10.1007/978-1-4939-1115-8_17 Text en © Springer Science+Business Media New York 2014 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Wang, Mingjun
Claesson, Mogens H.
Classification of Human Leukocyte Antigen (HLA) Supertypes
title Classification of Human Leukocyte Antigen (HLA) Supertypes
title_full Classification of Human Leukocyte Antigen (HLA) Supertypes
title_fullStr Classification of Human Leukocyte Antigen (HLA) Supertypes
title_full_unstemmed Classification of Human Leukocyte Antigen (HLA) Supertypes
title_short Classification of Human Leukocyte Antigen (HLA) Supertypes
title_sort classification of human leukocyte antigen (hla) supertypes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7121184/
https://www.ncbi.nlm.nih.gov/pubmed/25048132
http://dx.doi.org/10.1007/978-1-4939-1115-8_17
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