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Immunity to Placental Malaria. IV. Placental Malaria Is Associated with Up‐Regulation of Macrophage Migration Inhibitory Factor in Intervillous Blood
Author(s) -
Sujittra Chaisavaneeyakorn,
Julie M. Moore,
Caroline Othoro,
Juliana A. Otieno,
Sansanee C. Chaiyaroj,
Ya Ping Shi,
Bernard L. Nahlen,
Altaf A. Lal,
Venkatachalam Udhayakumar
Publication year - 2002
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/344322
Subject(s) - macrophage migration inhibitory factor , peripheral blood mononuclear cell , immunology , malaria , cord blood , macrophage , placenta , plasmodium falciparum , immune system , pregnancy , immunity , biology , blood plasma , medicine , endocrinology , fetus , cytokine , in vitro , biochemistry , genetics
Macrophage migration inhibitory factor (MIF) may play a role in immune responses to malaria during pregnancy by virtue of its ability to activate macrophages and to overcome the immunosuppressive effect of glucocorticoids. The present study investigated whether plasma MIF levels are altered in pregnant women with placental malaria (PM) and/or human immunodeficiency virus (HIV) infection. For the first time it is demonstrated that MIF levels in the intervillous blood (IVB) plasma were significantly elevated, compared with that in both peripheral plasma ( approximately 500-fold) and cord plasma (4.6-fold; P<.01). IVB mononuclear cells also produced significantly higher levels of MIF, compared with that of peripheral blood mononuclear cells. PM was associated with increased levels of MIF in the IVB plasma (P<.02). Primigravid and secundigravid women had significantly higher levels of MIF in their IVB plasma than did multigravid women (P<.05). HIV infection did not significantly alter MIF levels in any site examined.

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