Host response to malaria during pregnancy: placental monocyte recruitment is associated with elevated beta chemokine expression.

Malaria during pregnancy is associated with poor birth outcomes, particularly low birth weight. Recently, monocyte infiltration into the placental intervillous space has been identified as a key risk factor for low birth weight. However, the malaria-induced chemokines involved in recruiting and acti...

Full description

Bibliographic Details
Main Authors: Abrams, E, Brown, H, Chensue, S, Turner, G, Tadesse, E, Lema, V, Molyneux, M, Rochford, R, Meshnick, SR, Rogerson, S
Format: Journal article
Language:English
Published: 2003
_version_ 1797088316376481792
author Abrams, E
Brown, H
Chensue, S
Turner, G
Tadesse, E
Lema, V
Molyneux, M
Rochford, R
Meshnick, SR
Rogerson, S
author_facet Abrams, E
Brown, H
Chensue, S
Turner, G
Tadesse, E
Lema, V
Molyneux, M
Rochford, R
Meshnick, SR
Rogerson, S
author_sort Abrams, E
collection OXFORD
description Malaria during pregnancy is associated with poor birth outcomes, particularly low birth weight. Recently, monocyte infiltration into the placental intervillous space has been identified as a key risk factor for low birth weight. However, the malaria-induced chemokines involved in recruiting and activating placental monocytes have not been identified. In this study, we determined which chemokines are elevated during placental malaria infection and the association between chemokine expression and placental monocyte infiltration. Placental malaria infection was associated with elevations in mRNA expression of three beta chemokines, macrophage-inflammatory protein 1 (MIP-1) alpha (CCL3), monocyte chemoattractant protein 1 (MCP-1; CCL2), and I-309 (CCL1), and one alpha chemokine, IL-8 (CXCL8); all correlated with monocyte density in the placental intervillous space. Placental plasma concentrations of MIP-1 alpha and IL-8 were increased in women with placental malaria and were associated with placental monocyte infiltration. By immunohistochemistry, we localized placental chemokine production in malaria-infected placentas: some but not all hemozoin-laden maternal macrophages produced MIP-1 beta and MCP-1, and fetal stromal cells produced MCP-1. In sum, local placental production of chemokines is increased in malaria, and may be an important trigger for monocyte accumulation in the placenta.
first_indexed 2024-03-07T02:48:16Z
format Journal article
id oxford-uuid:acc4f363-e627-478f-abdf-3961282b6c29
institution University of Oxford
language English
last_indexed 2024-03-07T02:48:16Z
publishDate 2003
record_format dspace
spelling oxford-uuid:acc4f363-e627-478f-abdf-3961282b6c292022-03-27T03:31:13ZHost response to malaria during pregnancy: placental monocyte recruitment is associated with elevated beta chemokine expression.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:acc4f363-e627-478f-abdf-3961282b6c29EnglishSymplectic Elements at Oxford2003Abrams, EBrown, HChensue, STurner, GTadesse, ELema, VMolyneux, MRochford, RMeshnick, SRRogerson, SMalaria during pregnancy is associated with poor birth outcomes, particularly low birth weight. Recently, monocyte infiltration into the placental intervillous space has been identified as a key risk factor for low birth weight. However, the malaria-induced chemokines involved in recruiting and activating placental monocytes have not been identified. In this study, we determined which chemokines are elevated during placental malaria infection and the association between chemokine expression and placental monocyte infiltration. Placental malaria infection was associated with elevations in mRNA expression of three beta chemokines, macrophage-inflammatory protein 1 (MIP-1) alpha (CCL3), monocyte chemoattractant protein 1 (MCP-1; CCL2), and I-309 (CCL1), and one alpha chemokine, IL-8 (CXCL8); all correlated with monocyte density in the placental intervillous space. Placental plasma concentrations of MIP-1 alpha and IL-8 were increased in women with placental malaria and were associated with placental monocyte infiltration. By immunohistochemistry, we localized placental chemokine production in malaria-infected placentas: some but not all hemozoin-laden maternal macrophages produced MIP-1 beta and MCP-1, and fetal stromal cells produced MCP-1. In sum, local placental production of chemokines is increased in malaria, and may be an important trigger for monocyte accumulation in the placenta.
spellingShingle Abrams, E
Brown, H
Chensue, S
Turner, G
Tadesse, E
Lema, V
Molyneux, M
Rochford, R
Meshnick, SR
Rogerson, S
Host response to malaria during pregnancy: placental monocyte recruitment is associated with elevated beta chemokine expression.
title Host response to malaria during pregnancy: placental monocyte recruitment is associated with elevated beta chemokine expression.
title_full Host response to malaria during pregnancy: placental monocyte recruitment is associated with elevated beta chemokine expression.
title_fullStr Host response to malaria during pregnancy: placental monocyte recruitment is associated with elevated beta chemokine expression.
title_full_unstemmed Host response to malaria during pregnancy: placental monocyte recruitment is associated with elevated beta chemokine expression.
title_short Host response to malaria during pregnancy: placental monocyte recruitment is associated with elevated beta chemokine expression.
title_sort host response to malaria during pregnancy placental monocyte recruitment is associated with elevated beta chemokine expression
work_keys_str_mv AT abramse hostresponsetomalariaduringpregnancyplacentalmonocyterecruitmentisassociatedwithelevatedbetachemokineexpression
AT brownh hostresponsetomalariaduringpregnancyplacentalmonocyterecruitmentisassociatedwithelevatedbetachemokineexpression
AT chensues hostresponsetomalariaduringpregnancyplacentalmonocyterecruitmentisassociatedwithelevatedbetachemokineexpression
AT turnerg hostresponsetomalariaduringpregnancyplacentalmonocyterecruitmentisassociatedwithelevatedbetachemokineexpression
AT tadessee hostresponsetomalariaduringpregnancyplacentalmonocyterecruitmentisassociatedwithelevatedbetachemokineexpression
AT lemav hostresponsetomalariaduringpregnancyplacentalmonocyterecruitmentisassociatedwithelevatedbetachemokineexpression
AT molyneuxm hostresponsetomalariaduringpregnancyplacentalmonocyterecruitmentisassociatedwithelevatedbetachemokineexpression
AT rochfordr hostresponsetomalariaduringpregnancyplacentalmonocyterecruitmentisassociatedwithelevatedbetachemokineexpression
AT meshnicksr hostresponsetomalariaduringpregnancyplacentalmonocyterecruitmentisassociatedwithelevatedbetachemokineexpression
AT rogersons hostresponsetomalariaduringpregnancyplacentalmonocyterecruitmentisassociatedwithelevatedbetachemokineexpression