Cited by 71Malaria Research and ControlChemokine receptors and signalingPreterm Birth and Chorioamnionitis

Levels of Macrophage Inflammatory Protein 1α (MIP-1α) and MIP-1β in Intervillous Blood Plasma Samples from Women with Placental Malaria and Human Immunodeficiency Virus Infection

Open access
Chaisavaneeyakorn, Sujittra, Moore, Julie M., Mirel, Lisa, Othoro, Caroline, Otieno, Juliana, Chaiyaroj, Sansanee C., Shi, Ya Ping, Nahlen, Bernard L. +2 more·2003·Clinical and Vaccine Immunology

Abstract

Macrophage inflammatory protein-1α (MIP-1α) and MIP-1β 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-1β 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-1β than HIV-positive PM-negative women. The MIP-1α level was not altered in association with either infection. The IVB plasma levels of MIP-1α and MIP-1β 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-1β compared to PM-negative mothers, irrespective of their HIV infection status. MIP-1β and MIP-1α levels in PM-positive women were positively associated with parasite density and malaria pigment levels. Regardless of HIV serostatus, the IVB MIP-1β level was significantly lower in women with PM-associated anemia. In summary, an elevated level of MIP-1β was associated with PM. HIV infection did not significantly alter these two chemokine levels in IVB plasma.

Integrity signals

Registry

Crossref · 10.1128/cdli.10.4.631-636.2003

Cites

25 of 25 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • PM is associated with inflammatory immune responses, with increased levels of soluble mediators like TNF-α, TNF receptor I, TNF receptor II and IL-10 in peripheral blood.

    “PM is associated with inflammatory immune responses [75–79], with increased levels of soluble mediators like TNF-α, TNF receptor I, TNF receptor II and IL-10 in peripheral blood [80,81].”

    From Diagnosing malaria in pregnancy: An update (2012) · cites this paper as [78]

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Chaisavaneeyakorn, S., Moore, J. M., Mirel, L., Othoro, C., Otieno, J., Chaiyaroj, S. C., Shi, Y. P., Nahlen, B. L., Lal, A. A., & Udhayakumar, V.
Affiliations
Centers for Disease Control and Prevention (US)
Venue
Clinical and Vaccine Immunology
Published
2003-07
Volume
10
Issue
4
Pages
631-636
ISSN
  • 1556-679X (ISSN-L)
  • 1556-6811
OpenAlex
W2147783813
Cited by
71
References
25
Citations by year
2025: 2 · 2024: 3 · 2023: 4 · 2022: 1 · 2021: 2 · 2020: 5 · 2019: 5 · 2017: 3 · 2016: 1 · 2015: 1 · 2013: 8 · 2012: 9
FWCI
4.74
Type
journal article
Language
en
Open access
Locations
  • Clinical and Vaccine Immunology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • United States Agency for International Development
  • World Health Organization
  • Mahidol University
  • National Institutes of Health
  • Centers for Disease Control and Prevention
  • National Institute of Allergy and Infectious Diseases (R01AI050240, AI50240)
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Malaria Research and Control
  • Health Sciences › Medicine › Oncology › Chemokine receptors and signaling
  • Health Sciences › Medicine › Epidemiology › Preterm Birth and Chorioamnionitis
Keywords
macrophage inflammatory protein-1alpha, MIP-1β, chemokines, placental malaria, HIV coinfection, cord plasma, malaria parasite density, hemozoin, anemia
MeSH terms
Adult, Disease Susceptibility, Female, Fetal Blood, Gene Expression Regulation, Hemeproteins, Humans, Kenya, Malaria, Placenta Diseases, Plasma, Pregnancy, Pregnancy Complications, Infectious, Retrospective Studies, Cohort Studies, HIV Infections, Th1 Cells, Macrophage Inflammatory Proteins, Chemokine CCL3, Chemokine CCL4

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review