Placental Microparticles and MicroRNAs in Pregnant Women with Plasmodium falciparum or HIV Infection

PLoS One. 2016 Jan 12;11(1):e0146361. doi: 10.1371/journal.pone.0146361. eCollection 2016.

Abstract

Background: During pregnancy, syncytiotrophoblast vesicles contribute to maternal tolerance towards the fetus, but also to pathologies such as pre-eclampsia. The aim of the study was to address whether Plasmodium falciparum and HIV infections in pregnancy affect the secretion, microRNA content and function of trophoblast microparticles.

Methods: Microparticles were isolated and characterized from 122 peripheral plasmas of Mozambican pregnant women, malaria- and/or HIV-infected and non-infected. Expression of placenta-related microRNAs in microparticles was analysed by qPCR and the effect of circulating microparticles on dendritic cells assessed by phenotype analysis and cytokine/chemokine measurement.

Results: Concentrations of total and trophoblast microparticles detected by flow cytometry were higher in HIV-positive (P = 0.005 and P = 0.030, respectively) compared to non-infected mothers, as well as in women delivering low birthweight newborns (P = 0.032 and P = 0.021, respectively). miR-517c was overexpressed in mothers with placental malaria (P = 0.034), compared to non-infected. Microparticles from HIV-positive induced a higher expression of MHCII (P = 0.021) and lower production of MCP1 (P = 0.008) than microparticles from non-infected women.

Conclusions: In summary, alterations in total and trophoblast microparticles associated with malaria and HIV in pregnant women may have an immunopathogenic role. The potential for placental-derived vesicles and microRNAs as biomarkers of adverse outcomes during pregnancy and malaria infection should be confirmed in future studies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cell-Derived Microparticles / metabolism
  • Cell-Derived Microparticles / ultrastructure
  • Chemokines / metabolism
  • Demography
  • Dendritic Cells / metabolism
  • Female
  • HIV Infections / metabolism*
  • Humans
  • Infant, Newborn
  • Malaria, Falciparum / metabolism*
  • Malaria, Falciparum / pathology
  • MicroRNAs / metabolism*
  • Phenotype
  • Placenta / metabolism*
  • Plasmodium falciparum / physiology*
  • Pregnancy
  • Pregnancy Outcome
  • Trophoblasts / metabolism
  • Young Adult

Substances

  • Chemokines
  • MicroRNAs

Grants and funding

This work was supported by the Instituto de Salud Carlos III (PI13/01478, CES10/021-I3SNS to AM); the Banco de Bilbao, Vizcaya, Argentaria Foundation (BBVA02-0); the Ministerio de Ciencia e Innovación (RYC-2008-02631 to CD); the Institut d'Investigacions Biomèdiques August Pi i Sunyer (to LM) and the Departament d’Universitats i Recerca de la Generalitat de Catalunya [Agencia de Gestión de Ayudas Universitarias y de Investigación (AGAUR); grant 2014SGR263]. The Manhiça Health Research Centre receives core support from the Spanish Agency for International Cooperation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.