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Screening for C3 Deficiency in Newborns Using Microarrays
BACKGROUND: Dried blood spot samples (DBSS) from newborns are widely used in neonatal screening for selected metabolic diseases and diagnostic possibilities for additional disorders are continuously being evaluated. Primary immunodeficiency disorders comprise a group of more than one hundred disease...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2669175/ https://www.ncbi.nlm.nih.gov/pubmed/19390687 http://dx.doi.org/10.1371/journal.pone.0005321 |
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author | Janzi, Magdalena Sjöberg, Ronald Wan, Jinghong Fischler, Björn von Döbeln, Ulrika Isaac, Lourdes Nilsson, Peter Hammarström, Lennart |
author_facet | Janzi, Magdalena Sjöberg, Ronald Wan, Jinghong Fischler, Björn von Döbeln, Ulrika Isaac, Lourdes Nilsson, Peter Hammarström, Lennart |
author_sort | Janzi, Magdalena |
collection | PubMed |
description | BACKGROUND: Dried blood spot samples (DBSS) from newborns are widely used in neonatal screening for selected metabolic diseases and diagnostic possibilities for additional disorders are continuously being evaluated. Primary immunodeficiency disorders comprise a group of more than one hundred diseases, several of which are fatal early in life. Yet, a majority of the patients are not diagnosed due to lack of high-throughput screening methods. METHODOLOGY/PRINCIPAL FINDINGS: We have previously developed a system using reverse phase protein microarrays for analysis of IgA levels in serum samples. In this study, we extended the applicability of the method to include determination of complement component C3 levels in eluates from DBSS collected at birth. Normal levels of C3 were readily detected in 269 DBSS from healthy newborns, while no C3 was detected in sera and DBSS from C3 deficient patients. CONCLUSIONS/SIGNIFICANCE: The findings suggest that patients with deficiencies of specific serum proteins can be identified by analysis of DBSS using reverse phase protein microarrays. |
format | Text |
id | pubmed-2669175 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-26691752009-04-24 Screening for C3 Deficiency in Newborns Using Microarrays Janzi, Magdalena Sjöberg, Ronald Wan, Jinghong Fischler, Björn von Döbeln, Ulrika Isaac, Lourdes Nilsson, Peter Hammarström, Lennart PLoS One Research Article BACKGROUND: Dried blood spot samples (DBSS) from newborns are widely used in neonatal screening for selected metabolic diseases and diagnostic possibilities for additional disorders are continuously being evaluated. Primary immunodeficiency disorders comprise a group of more than one hundred diseases, several of which are fatal early in life. Yet, a majority of the patients are not diagnosed due to lack of high-throughput screening methods. METHODOLOGY/PRINCIPAL FINDINGS: We have previously developed a system using reverse phase protein microarrays for analysis of IgA levels in serum samples. In this study, we extended the applicability of the method to include determination of complement component C3 levels in eluates from DBSS collected at birth. Normal levels of C3 were readily detected in 269 DBSS from healthy newborns, while no C3 was detected in sera and DBSS from C3 deficient patients. CONCLUSIONS/SIGNIFICANCE: The findings suggest that patients with deficiencies of specific serum proteins can be identified by analysis of DBSS using reverse phase protein microarrays. Public Library of Science 2009-04-24 /pmc/articles/PMC2669175/ /pubmed/19390687 http://dx.doi.org/10.1371/journal.pone.0005321 Text en Janzi et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Janzi, Magdalena Sjöberg, Ronald Wan, Jinghong Fischler, Björn von Döbeln, Ulrika Isaac, Lourdes Nilsson, Peter Hammarström, Lennart Screening for C3 Deficiency in Newborns Using Microarrays |
title | Screening for C3 Deficiency in Newborns Using Microarrays |
title_full | Screening for C3 Deficiency in Newborns Using Microarrays |
title_fullStr | Screening for C3 Deficiency in Newborns Using Microarrays |
title_full_unstemmed | Screening for C3 Deficiency in Newborns Using Microarrays |
title_short | Screening for C3 Deficiency in Newborns Using Microarrays |
title_sort | screening for c3 deficiency in newborns using microarrays |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2669175/ https://www.ncbi.nlm.nih.gov/pubmed/19390687 http://dx.doi.org/10.1371/journal.pone.0005321 |
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