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Monocytes and macrophages and placental malaria infections in an area of unstable malaria transmission in eastern Sudan

BACKGROUND: Maternal immunity is thought to play a major role in the increased susceptibility of pregnant women to Plasmodium falciparum malaria. Few studies exist on immunohistochemical characterization of the placental inflammatory infiltrate. The current study was conducted in Gadarif hospital in...

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Autores principales: Salih, Magdi M, Mohammed, Amal H, Mohmmed, Ahmed A, Adam, Gamal K, Elbashir, Mustafa I, Adam, Ishag
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182959/
https://www.ncbi.nlm.nih.gov/pubmed/21929772
http://dx.doi.org/10.1186/1746-1596-6-83
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author Salih, Magdi M
Mohammed, Amal H
Mohmmed, Ahmed A
Adam, Gamal K
Elbashir, Mustafa I
Adam, Ishag
author_facet Salih, Magdi M
Mohammed, Amal H
Mohmmed, Ahmed A
Adam, Gamal K
Elbashir, Mustafa I
Adam, Ishag
author_sort Salih, Magdi M
collection PubMed
description BACKGROUND: Maternal immunity is thought to play a major role in the increased susceptibility of pregnant women to Plasmodium falciparum malaria. Few studies exist on immunohistochemical characterization of the placental inflammatory infiltrate. The current study was conducted in Gadarif hospital in an area characterized by unstable malaria transmission in eastern Sudan. METHOD: Ninety three placentae were investigated for malaria histological changes and immunohistochemical study for monocytes and macrophages (CD68). RESULTS: While 1(1.1%), 2(2.2%) and 20(21.5%) of the 93 placentae had acute, chronic and past malaria infections, 70(75.2%) had no malaria infections. Monocytes and macrophage (CD 68) were detected in 29 (31.2%) of these 93 placentae. Significantly higher rate of monocytes and macrophage were detected in placentae with malaria infections [11/23 (47.8%) vs. 18/70 (25.7%); P = 0.047] especially in placentae with past malaria infections. Placental malaria infections and monocytes and macrophages cells infiltration were not different between primiparae and multiparae. There was no significant difference in the birth weight between the women with placental malaria infections/monocytes and macrophages cells infiltration and those who had no placental malaria infections/cellular infiltrations. CONCLUSION: Significantly higher rate of monocytes and macrophage were detected in placentae with malaria infections. Neither placental malaria infections nor cellular infiltrates were associated with parity or lead to reduction of birth weight.
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spelling pubmed-31829592011-09-30 Monocytes and macrophages and placental malaria infections in an area of unstable malaria transmission in eastern Sudan Salih, Magdi M Mohammed, Amal H Mohmmed, Ahmed A Adam, Gamal K Elbashir, Mustafa I Adam, Ishag Diagn Pathol Research BACKGROUND: Maternal immunity is thought to play a major role in the increased susceptibility of pregnant women to Plasmodium falciparum malaria. Few studies exist on immunohistochemical characterization of the placental inflammatory infiltrate. The current study was conducted in Gadarif hospital in an area characterized by unstable malaria transmission in eastern Sudan. METHOD: Ninety three placentae were investigated for malaria histological changes and immunohistochemical study for monocytes and macrophages (CD68). RESULTS: While 1(1.1%), 2(2.2%) and 20(21.5%) of the 93 placentae had acute, chronic and past malaria infections, 70(75.2%) had no malaria infections. Monocytes and macrophage (CD 68) were detected in 29 (31.2%) of these 93 placentae. Significantly higher rate of monocytes and macrophage were detected in placentae with malaria infections [11/23 (47.8%) vs. 18/70 (25.7%); P = 0.047] especially in placentae with past malaria infections. Placental malaria infections and monocytes and macrophages cells infiltration were not different between primiparae and multiparae. There was no significant difference in the birth weight between the women with placental malaria infections/monocytes and macrophages cells infiltration and those who had no placental malaria infections/cellular infiltrations. CONCLUSION: Significantly higher rate of monocytes and macrophage were detected in placentae with malaria infections. Neither placental malaria infections nor cellular infiltrates were associated with parity or lead to reduction of birth weight. BioMed Central 2011-09-19 /pmc/articles/PMC3182959/ /pubmed/21929772 http://dx.doi.org/10.1186/1746-1596-6-83 Text en Copyright ©2011 Salih 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
Salih, Magdi M
Mohammed, Amal H
Mohmmed, Ahmed A
Adam, Gamal K
Elbashir, Mustafa I
Adam, Ishag
Monocytes and macrophages and placental malaria infections in an area of unstable malaria transmission in eastern Sudan
title Monocytes and macrophages and placental malaria infections in an area of unstable malaria transmission in eastern Sudan
title_full Monocytes and macrophages and placental malaria infections in an area of unstable malaria transmission in eastern Sudan
title_fullStr Monocytes and macrophages and placental malaria infections in an area of unstable malaria transmission in eastern Sudan
title_full_unstemmed Monocytes and macrophages and placental malaria infections in an area of unstable malaria transmission in eastern Sudan
title_short Monocytes and macrophages and placental malaria infections in an area of unstable malaria transmission in eastern Sudan
title_sort monocytes and macrophages and placental malaria infections in an area of unstable malaria transmission in eastern sudan
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182959/
https://www.ncbi.nlm.nih.gov/pubmed/21929772
http://dx.doi.org/10.1186/1746-1596-6-83
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