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Underweight Full-Term Indian Neonates Show Differences in Umbilical Cord Blood Leukocyte Phenotype: A Cross-Sectional Study

BACKGROUND: While infections are a major cause of neonatal mortality in India even in full-term neonates, this is an especial problem in the large proportion (~20%) of neonates born underweight (or small-for-gestational-age; SGA). One potential contributory factor for this susceptibility is the poss...

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Autores principales: Rathore, Deepak K., Nair, Deepa, Raza, Saimah, Saini, Savita, Singh, Reeta, Kumar, Amit, Tripathi, Reva, Ramji, Siddarth, Batra, Aruna, Aggarwal, Kailash C., Chellani, Harish K., Arya, Sugandha, Bhatla, Neerja, Paul, Vinod K., Aggarwal, Ramesh, Agarwal, Nidhi, Mehta, Umesh, Sopory, Shailaja, Natchu, Uma Chandra Mouli, Bhatnagar, Shinjini, Bal, Vineeta, Rath, Satyajit, Wadhwa, Nitya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4405369/
https://www.ncbi.nlm.nih.gov/pubmed/25898362
http://dx.doi.org/10.1371/journal.pone.0123589
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author Rathore, Deepak K.
Nair, Deepa
Raza, Saimah
Saini, Savita
Singh, Reeta
Kumar, Amit
Tripathi, Reva
Ramji, Siddarth
Batra, Aruna
Aggarwal, Kailash C.
Chellani, Harish K.
Arya, Sugandha
Bhatla, Neerja
Paul, Vinod K.
Aggarwal, Ramesh
Agarwal, Nidhi
Mehta, Umesh
Sopory, Shailaja
Natchu, Uma Chandra Mouli
Bhatnagar, Shinjini
Bal, Vineeta
Rath, Satyajit
Wadhwa, Nitya
author_facet Rathore, Deepak K.
Nair, Deepa
Raza, Saimah
Saini, Savita
Singh, Reeta
Kumar, Amit
Tripathi, Reva
Ramji, Siddarth
Batra, Aruna
Aggarwal, Kailash C.
Chellani, Harish K.
Arya, Sugandha
Bhatla, Neerja
Paul, Vinod K.
Aggarwal, Ramesh
Agarwal, Nidhi
Mehta, Umesh
Sopory, Shailaja
Natchu, Uma Chandra Mouli
Bhatnagar, Shinjini
Bal, Vineeta
Rath, Satyajit
Wadhwa, Nitya
author_sort Rathore, Deepak K.
collection PubMed
description BACKGROUND: While infections are a major cause of neonatal mortality in India even in full-term neonates, this is an especial problem in the large proportion (~20%) of neonates born underweight (or small-for-gestational-age; SGA). One potential contributory factor for this susceptibility is the possibility that immune system maturation may be affected along with intrauterine growth retardation. METHODS: In order to examine the possibility that differences in immune status may underlie the susceptibility of SGA neonates to infections, we enumerated the frequencies and concentrations of 22 leukocyte subset populations as well as IgM and IgA levels in umbilical cord blood from full-term SGA neonates and compared them with values from normal-weight (or appropriate-for-gestational-age; AGA) full-term neonates. We eliminated most SGA-associated risk factors in the exclusion criteria so as to ensure that AGA-SGA differences, if any, would be more likely to be associated with the underweight status itself. RESULTS: An analysis of 502 such samples, including 50 from SGA neonates, showed that SGA neonates have significantly fewer plasmacytoid dendritic cells (pDCs), a higher myeloid DC (mDC) to pDC ratio, more natural killer (NK) cells, and higher IgM levels in cord blood in comparison with AGA neonates. Other differences were also observed such as tendencies to lower CD4:CD8 ratios and greater prominence of inflammatory monocytes, mDCs and neutrophils, but while some of them had substantial differences, they did not quite reach the standard level of statistical significance. CONCLUSIONS: These differences in cellular lineages of the immune system possibly reflect stress responses in utero associated with growth restriction. Increased susceptibility to infections may thus be linked to complex immune system dysregulation rather than simply retarded immune system maturation.
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spelling pubmed-44053692015-05-07 Underweight Full-Term Indian Neonates Show Differences in Umbilical Cord Blood Leukocyte Phenotype: A Cross-Sectional Study Rathore, Deepak K. Nair, Deepa Raza, Saimah Saini, Savita Singh, Reeta Kumar, Amit Tripathi, Reva Ramji, Siddarth Batra, Aruna Aggarwal, Kailash C. Chellani, Harish K. Arya, Sugandha Bhatla, Neerja Paul, Vinod K. Aggarwal, Ramesh Agarwal, Nidhi Mehta, Umesh Sopory, Shailaja Natchu, Uma Chandra Mouli Bhatnagar, Shinjini Bal, Vineeta Rath, Satyajit Wadhwa, Nitya PLoS One Research Article BACKGROUND: While infections are a major cause of neonatal mortality in India even in full-term neonates, this is an especial problem in the large proportion (~20%) of neonates born underweight (or small-for-gestational-age; SGA). One potential contributory factor for this susceptibility is the possibility that immune system maturation may be affected along with intrauterine growth retardation. METHODS: In order to examine the possibility that differences in immune status may underlie the susceptibility of SGA neonates to infections, we enumerated the frequencies and concentrations of 22 leukocyte subset populations as well as IgM and IgA levels in umbilical cord blood from full-term SGA neonates and compared them with values from normal-weight (or appropriate-for-gestational-age; AGA) full-term neonates. We eliminated most SGA-associated risk factors in the exclusion criteria so as to ensure that AGA-SGA differences, if any, would be more likely to be associated with the underweight status itself. RESULTS: An analysis of 502 such samples, including 50 from SGA neonates, showed that SGA neonates have significantly fewer plasmacytoid dendritic cells (pDCs), a higher myeloid DC (mDC) to pDC ratio, more natural killer (NK) cells, and higher IgM levels in cord blood in comparison with AGA neonates. Other differences were also observed such as tendencies to lower CD4:CD8 ratios and greater prominence of inflammatory monocytes, mDCs and neutrophils, but while some of them had substantial differences, they did not quite reach the standard level of statistical significance. CONCLUSIONS: These differences in cellular lineages of the immune system possibly reflect stress responses in utero associated with growth restriction. Increased susceptibility to infections may thus be linked to complex immune system dysregulation rather than simply retarded immune system maturation. Public Library of Science 2015-04-21 /pmc/articles/PMC4405369/ /pubmed/25898362 http://dx.doi.org/10.1371/journal.pone.0123589 Text en © 2015 Rathore 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
Rathore, Deepak K.
Nair, Deepa
Raza, Saimah
Saini, Savita
Singh, Reeta
Kumar, Amit
Tripathi, Reva
Ramji, Siddarth
Batra, Aruna
Aggarwal, Kailash C.
Chellani, Harish K.
Arya, Sugandha
Bhatla, Neerja
Paul, Vinod K.
Aggarwal, Ramesh
Agarwal, Nidhi
Mehta, Umesh
Sopory, Shailaja
Natchu, Uma Chandra Mouli
Bhatnagar, Shinjini
Bal, Vineeta
Rath, Satyajit
Wadhwa, Nitya
Underweight Full-Term Indian Neonates Show Differences in Umbilical Cord Blood Leukocyte Phenotype: A Cross-Sectional Study
title Underweight Full-Term Indian Neonates Show Differences in Umbilical Cord Blood Leukocyte Phenotype: A Cross-Sectional Study
title_full Underweight Full-Term Indian Neonates Show Differences in Umbilical Cord Blood Leukocyte Phenotype: A Cross-Sectional Study
title_fullStr Underweight Full-Term Indian Neonates Show Differences in Umbilical Cord Blood Leukocyte Phenotype: A Cross-Sectional Study
title_full_unstemmed Underweight Full-Term Indian Neonates Show Differences in Umbilical Cord Blood Leukocyte Phenotype: A Cross-Sectional Study
title_short Underweight Full-Term Indian Neonates Show Differences in Umbilical Cord Blood Leukocyte Phenotype: A Cross-Sectional Study
title_sort underweight full-term indian neonates show differences in umbilical cord blood leukocyte phenotype: a cross-sectional study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4405369/
https://www.ncbi.nlm.nih.gov/pubmed/25898362
http://dx.doi.org/10.1371/journal.pone.0123589
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