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Length Variation of DC-SIGN and L-SIGN Neck-Region has no Impact on Tuberculosis Susceptibility
The C-type lectins DC-SIGN and L-SIGN are important pathogen-recognition receptors of the human innate immune system. Both lectins have been shown to interact with a vast range of infectious agents, including Mycobacterium tuberculosis, the etiologic agent of tuberculosis in humans. In addition, DC-...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc.
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132702/ https://www.ncbi.nlm.nih.gov/pubmed/17321900 http://dx.doi.org/10.1016/j.humimm.2006.10.020 |
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author | Barreiro, Luis B. Neyrolles, Olivier Babb, Chantal L. van Helden, Paul D. Gicquel, Brigitte Hoal, Eileen G. Quintana-Murci, Lluís |
author_facet | Barreiro, Luis B. Neyrolles, Olivier Babb, Chantal L. van Helden, Paul D. Gicquel, Brigitte Hoal, Eileen G. Quintana-Murci, Lluís |
author_sort | Barreiro, Luis B. |
collection | PubMed |
description | The C-type lectins DC-SIGN and L-SIGN are important pathogen-recognition receptors of the human innate immune system. Both lectins have been shown to interact with a vast range of infectious agents, including Mycobacterium tuberculosis, the etiologic agent of tuberculosis in humans. In addition, DC-SIGN and L-SIGN possess a neck region, made up of a variable number of 23 amino acid tandem repeats, which plays a crucial role in the tetramerization of these proteins and support of the carbohydrate recognition domain. The length of the neck region, which shows variable levels of polymorphism, can critically influence the pathogen binding properties of these two receptors. We therefore investigated the impact of the DC-SIGN and L-SIGN neck-region length variation on the outcome of tuberculosis by screening this polymorphism in a large cohort of Coloured South African origin. The analyses of 711 individuals, including 351 tuberculosis patients and 360 healthy controls, revealed that none of the DC-SIGN and L-SIGN neck-region variants or genotypes seems to influence the individual susceptibility to develop tuberculosis. |
format | Online Article Text |
id | pubmed-7132702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71327022020-04-08 Length Variation of DC-SIGN and L-SIGN Neck-Region has no Impact on Tuberculosis Susceptibility Barreiro, Luis B. Neyrolles, Olivier Babb, Chantal L. van Helden, Paul D. Gicquel, Brigitte Hoal, Eileen G. Quintana-Murci, Lluís Hum Immunol Article The C-type lectins DC-SIGN and L-SIGN are important pathogen-recognition receptors of the human innate immune system. Both lectins have been shown to interact with a vast range of infectious agents, including Mycobacterium tuberculosis, the etiologic agent of tuberculosis in humans. In addition, DC-SIGN and L-SIGN possess a neck region, made up of a variable number of 23 amino acid tandem repeats, which plays a crucial role in the tetramerization of these proteins and support of the carbohydrate recognition domain. The length of the neck region, which shows variable levels of polymorphism, can critically influence the pathogen binding properties of these two receptors. We therefore investigated the impact of the DC-SIGN and L-SIGN neck-region length variation on the outcome of tuberculosis by screening this polymorphism in a large cohort of Coloured South African origin. The analyses of 711 individuals, including 351 tuberculosis patients and 360 healthy controls, revealed that none of the DC-SIGN and L-SIGN neck-region variants or genotypes seems to influence the individual susceptibility to develop tuberculosis. American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. 2007-02 2006-12-04 /pmc/articles/PMC7132702/ /pubmed/17321900 http://dx.doi.org/10.1016/j.humimm.2006.10.020 Text en Copyright © 2007 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Barreiro, Luis B. Neyrolles, Olivier Babb, Chantal L. van Helden, Paul D. Gicquel, Brigitte Hoal, Eileen G. Quintana-Murci, Lluís Length Variation of DC-SIGN and L-SIGN Neck-Region has no Impact on Tuberculosis Susceptibility |
title | Length Variation of DC-SIGN and L-SIGN Neck-Region has no Impact on Tuberculosis Susceptibility |
title_full | Length Variation of DC-SIGN and L-SIGN Neck-Region has no Impact on Tuberculosis Susceptibility |
title_fullStr | Length Variation of DC-SIGN and L-SIGN Neck-Region has no Impact on Tuberculosis Susceptibility |
title_full_unstemmed | Length Variation of DC-SIGN and L-SIGN Neck-Region has no Impact on Tuberculosis Susceptibility |
title_short | Length Variation of DC-SIGN and L-SIGN Neck-Region has no Impact on Tuberculosis Susceptibility |
title_sort | length variation of dc-sign and l-sign neck-region has no impact on tuberculosis susceptibility |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132702/ https://www.ncbi.nlm.nih.gov/pubmed/17321900 http://dx.doi.org/10.1016/j.humimm.2006.10.020 |
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