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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...

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Detalles Bibliográficos
Autores principales: Janzi, Magdalena, Sjöberg, Ronald, Wan, Jinghong, Fischler, Björn, von Döbeln, Ulrika, Isaac, Lourdes, Nilsson, Peter, Hammarström, Lennart
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
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.
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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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