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Galactofuranose antigens, a target for diagnosis of fungal infections in humans
The use of biomarkers for the detection of fungal infections is of interest to complement histopathological and culture methods. Since the production of antibodies in immunocompromised patients is scarce, detection of a specific antigen could be effective for early diagnosis. D-Galactofuranose (Galf...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Future Science Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5583699/ https://www.ncbi.nlm.nih.gov/pubmed/28883999 http://dx.doi.org/10.4155/fsoa-2017-0030 |
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author | Marino, Carla Rinflerch, Adriana de Lederkremer, Rosa M |
author_facet | Marino, Carla Rinflerch, Adriana de Lederkremer, Rosa M |
author_sort | Marino, Carla |
collection | PubMed |
description | The use of biomarkers for the detection of fungal infections is of interest to complement histopathological and culture methods. Since the production of antibodies in immunocompromised patients is scarce, detection of a specific antigen could be effective for early diagnosis. D-Galactofuranose (Galf) is the antigenic epitope in glycoconjugates of several pathogenic fungi. Since Galf is not biosynthesized by mammals, it is an attractive candidate for diagnosis of infection. A monoclonal antibody that recognizes Galf is commercialized for detection of aspergillosis. The linkage of Galf in the natural glycans and the chemical structures of the synthesized Galf-containing oligosaccharides are described in this paper. The oligosaccharides could be used for the synthesis of artificial carbohydrate-based antigens, not enough exploited for diagnosis. |
format | Online Article Text |
id | pubmed-5583699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Future Science Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-55836992017-09-07 Galactofuranose antigens, a target for diagnosis of fungal infections in humans Marino, Carla Rinflerch, Adriana de Lederkremer, Rosa M Future Sci OA Special Report The use of biomarkers for the detection of fungal infections is of interest to complement histopathological and culture methods. Since the production of antibodies in immunocompromised patients is scarce, detection of a specific antigen could be effective for early diagnosis. D-Galactofuranose (Galf) is the antigenic epitope in glycoconjugates of several pathogenic fungi. Since Galf is not biosynthesized by mammals, it is an attractive candidate for diagnosis of infection. A monoclonal antibody that recognizes Galf is commercialized for detection of aspergillosis. The linkage of Galf in the natural glycans and the chemical structures of the synthesized Galf-containing oligosaccharides are described in this paper. The oligosaccharides could be used for the synthesis of artificial carbohydrate-based antigens, not enough exploited for diagnosis. Future Science Ltd 2017-06-01 /pmc/articles/PMC5583699/ /pubmed/28883999 http://dx.doi.org/10.4155/fsoa-2017-0030 Text en © Rosa M de Lederkremer This work is licensed under a Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Special Report Marino, Carla Rinflerch, Adriana de Lederkremer, Rosa M Galactofuranose antigens, a target for diagnosis of fungal infections in humans |
title | Galactofuranose antigens, a target for diagnosis of fungal infections in humans |
title_full | Galactofuranose antigens, a target for diagnosis of fungal infections in humans |
title_fullStr | Galactofuranose antigens, a target for diagnosis of fungal infections in humans |
title_full_unstemmed | Galactofuranose antigens, a target for diagnosis of fungal infections in humans |
title_short | Galactofuranose antigens, a target for diagnosis of fungal infections in humans |
title_sort | galactofuranose antigens, a target for diagnosis of fungal infections in humans |
topic | Special Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5583699/ https://www.ncbi.nlm.nih.gov/pubmed/28883999 http://dx.doi.org/10.4155/fsoa-2017-0030 |
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