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CD20, CD3, placental malaria infections and low birth weight in an area of unstable malaria transmission in Central Sudan

BACKGROUND: Malaria during pregnancy is the main cause of low birth weight (LBW) in the tropics. There are few studies concerning B and T lymphocyte infiltrates in placental malaria infections or their potential association with LBW babies. METHODS: A case–control study was conducted at the Medani H...

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Autores principales: Batran, Samah E, Salih, Magdi M, Elhassan, Elhassan M, Mohmmed, Ahmed A, Adam, Ishag
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937234/
https://www.ncbi.nlm.nih.gov/pubmed/24245949
http://dx.doi.org/10.1186/1746-1596-8-189
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author Batran, Samah E
Salih, Magdi M
Elhassan, Elhassan M
Mohmmed, Ahmed A
Adam, Ishag
author_facet Batran, Samah E
Salih, Magdi M
Elhassan, Elhassan M
Mohmmed, Ahmed A
Adam, Ishag
author_sort Batran, Samah E
collection PubMed
description BACKGROUND: Malaria during pregnancy is the main cause of low birth weight (LBW) in the tropics. There are few studies concerning B and T lymphocyte infiltrates in placental malaria infections or their potential association with LBW babies. METHODS: A case–control study was conducted at the Medani Hospital, Central Sudan. Cases were women who had LBW deliveries (infants weighed < 2,500 g) and controls were parturient women with normal birth weight babies. Sociodemographic and medical characteristics were gathered from both groups of women using questionnaires. Cases and controls were investigated for malaria using microscopic blood film analysis, placental histology, and immunohistochemistry for detection of B (CD20) and T lymphocytes (CD3). RESULTS: The two groups (97 in each arm) were well matched in their basic characteristics. There were no malaria-positive blood films in either the cases or the controls. Twenty-nine (30.0%) vs. 24 (24.7%), P = 0.519 of the cases vs. the controls had placental malaria infections on histological examination. Three (3.1%), two (2.1%) and 24 (24.7%) vs. two (2.1%), two (2.1%) and 20 (20.6%) of the placentae showed evidence of acute, chronic and past malarial infections on histopathological examination of the two groups (case–control), respectively, while 68 (70.1%) vs. 73 (75.3%) of them showed no signs of infection; P = 0.420. Women with placental malaria infections had significantly fewer CD20 cell infiltrates [6 (11.3% vs. 95 (67.4%), P < 0.001)] and higher numbers of CD3 cell infiltrates [50 (94.3%) vs. 42 (29.8%), P < 0.001] than those without placental malaria infection. Logistic regression analysis showed that neither placental malaria infections nor CD3 or CD20 were associated with LBW. CONCLUSIONS: Significantly higher rates of CD3 T cells and lower rates of CD20 B cells were found in women with placental malaria infections compared with those without such infections. Neither placental malaria infection nor CD3 or CD20 are associated with LBW. VIRTUAL SLIDES: http://www.diagnosticpathology.diagnomx.eu/vs/6879723961063755
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spelling pubmed-39372342014-02-28 CD20, CD3, placental malaria infections and low birth weight in an area of unstable malaria transmission in Central Sudan Batran, Samah E Salih, Magdi M Elhassan, Elhassan M Mohmmed, Ahmed A Adam, Ishag Diagn Pathol Research BACKGROUND: Malaria during pregnancy is the main cause of low birth weight (LBW) in the tropics. There are few studies concerning B and T lymphocyte infiltrates in placental malaria infections or their potential association with LBW babies. METHODS: A case–control study was conducted at the Medani Hospital, Central Sudan. Cases were women who had LBW deliveries (infants weighed < 2,500 g) and controls were parturient women with normal birth weight babies. Sociodemographic and medical characteristics were gathered from both groups of women using questionnaires. Cases and controls were investigated for malaria using microscopic blood film analysis, placental histology, and immunohistochemistry for detection of B (CD20) and T lymphocytes (CD3). RESULTS: The two groups (97 in each arm) were well matched in their basic characteristics. There were no malaria-positive blood films in either the cases or the controls. Twenty-nine (30.0%) vs. 24 (24.7%), P = 0.519 of the cases vs. the controls had placental malaria infections on histological examination. Three (3.1%), two (2.1%) and 24 (24.7%) vs. two (2.1%), two (2.1%) and 20 (20.6%) of the placentae showed evidence of acute, chronic and past malarial infections on histopathological examination of the two groups (case–control), respectively, while 68 (70.1%) vs. 73 (75.3%) of them showed no signs of infection; P = 0.420. Women with placental malaria infections had significantly fewer CD20 cell infiltrates [6 (11.3% vs. 95 (67.4%), P < 0.001)] and higher numbers of CD3 cell infiltrates [50 (94.3%) vs. 42 (29.8%), P < 0.001] than those without placental malaria infection. Logistic regression analysis showed that neither placental malaria infections nor CD3 or CD20 were associated with LBW. CONCLUSIONS: Significantly higher rates of CD3 T cells and lower rates of CD20 B cells were found in women with placental malaria infections compared with those without such infections. Neither placental malaria infection nor CD3 or CD20 are associated with LBW. VIRTUAL SLIDES: http://www.diagnosticpathology.diagnomx.eu/vs/6879723961063755 BioMed Central 2013-11-18 /pmc/articles/PMC3937234/ /pubmed/24245949 http://dx.doi.org/10.1186/1746-1596-8-189 Text en Copyright © 2013 Batran et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Batran, Samah E
Salih, Magdi M
Elhassan, Elhassan M
Mohmmed, Ahmed A
Adam, Ishag
CD20, CD3, placental malaria infections and low birth weight in an area of unstable malaria transmission in Central Sudan
title CD20, CD3, placental malaria infections and low birth weight in an area of unstable malaria transmission in Central Sudan
title_full CD20, CD3, placental malaria infections and low birth weight in an area of unstable malaria transmission in Central Sudan
title_fullStr CD20, CD3, placental malaria infections and low birth weight in an area of unstable malaria transmission in Central Sudan
title_full_unstemmed CD20, CD3, placental malaria infections and low birth weight in an area of unstable malaria transmission in Central Sudan
title_short CD20, CD3, placental malaria infections and low birth weight in an area of unstable malaria transmission in Central Sudan
title_sort cd20, cd3, placental malaria infections and low birth weight in an area of unstable malaria transmission in central sudan
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937234/
https://www.ncbi.nlm.nih.gov/pubmed/24245949
http://dx.doi.org/10.1186/1746-1596-8-189
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