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Levels of macrophage inflammatory protein 1 alpha (MIP-1 alpha) and MIP-1 beta in intervillous blood plasma samples from women with placental malaria and human immunodeficiency virus infection.

Abstract
Macrophage inflammatory protein-1 alpha (MIP-1 alpha) and MIP-1 beta play an important role in modulating immune responses. To understand their importance in immunity to placental malaria (PM) and in human immunodeficiency virus (HIV)-PM coinfection, we investigated levels of these chemokines in the placental intervillous blood plasma (IVB plasma) and cord blood plasma of HIV-negative PM-negative, HIV-negative PM-positive, HIV-positive PM-negative, and HIV-positive PM-positive women. Compared to HIV-negative PM-negative women, the MIP-1 beta concentration in IVB plasma was significantly elevated in HIV-negative PM-positive women and HIV-positive PM-positive women, but it was unaltered in HIV-positive PM-negative women. Also, PM-infected women, irrespective of their HIV status, had significantly higher levels of MIP-1 beta than HIV-positive PM-negative women. The MIP-1 alpha level was not altered in association with either infection. The IVB plasma levels of MIP-1 alpha and MIP-1 beta positively correlated with the cord blood plasma levels of these chemokines. As with IVB plasma, only cord plasma from PM-infected mothers had significantly elevated levels of MIP-1 beta compared to PM-negative mothers, irrespective of their HIV infection status. MIP-1 beta and MIP-1 alpha levels in PM-positive women were positively associated with parasite density and malaria pigment levels. Regardless of HIV serostatus, the IVB MIP-1 beta level was significantly lower in women with PM-associated anemia. In summary, an elevated level of MIP-1 beta was associated with PM. HIV infection did not significantly alter these two chemokine levels in IVB plasma.
AuthorsSujittra Chaisavaneeyakorn, Julie M Moore, Lisa Mirel, Caroline Othoro, Juliana Otieno, Sansanee C Chaiyaroj, Ya Ping Shi, Bernard L Nahlen, Altaf A Lal, Venkatachalam Udhayakumar
JournalClinical and diagnostic laboratory immunology (Clin Diagn Lab Immunol) Vol. 10 Issue 4 Pg. 631-6 (Jul 2003) ISSN: 1071-412X [Print] United States
PMID12853396 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Chemokine CCL3
  • Chemokine CCL4
  • Hemeproteins
  • Macrophage Inflammatory Proteins
  • hemozoin
Topics
  • Adult
  • Chemokine CCL3
  • Chemokine CCL4
  • Cohort Studies
  • Disease Susceptibility
  • Female
  • Fetal Blood (chemistry)
  • Gene Expression Regulation
  • HIV Infections (blood)
  • Hemeproteins (analysis, physiology)
  • Humans
  • Kenya (epidemiology)
  • Macrophage Inflammatory Proteins (biosynthesis, blood, genetics)
  • Malaria (blood)
  • Placenta Diseases (blood)
  • Plasma
  • Pregnancy
  • Pregnancy Complications, Infectious (blood)
  • Retrospective Studies
  • Th1 Cells (immunology)

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