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Adhesion of Plasmodium falciparum infected erythrocytes in ex vivo perfused placental tissue : A novel model of placental malaria

Pehrson, Caroline (author)
University of Copenhagen
Mathiesen, Line (author)
University of Copenhagen
Heno, Kristine K. (author)
University of Copenhagen
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Salanti, Ali (author)
University of Copenhagen
Resende, Mafalda (author)
University of Copenhagen
Dzikowski, Ron (author)
Hebrew University-Hadassah Medical School
Damm, Peter (author)
University of Copenhagen
Hansson, Stefan (author)
Lund University,Lunds universitet,Obstetrik och gynekologi, Lund,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Obstetrics and Gynaecology (Lund),Section V,Department of Clinical Sciences, Lund,Faculty of Medicine
King, Christopher L. (author)
Case Western Reserve University
Schneider, Henning (author)
University of Bern
Wang, Christian W. (author)
University of Copenhagen
Lavstsen, Thomas (author)
University of Copenhagen
Theander, Thor G. (author)
University of Copenhagen
Knudsen, Lisbeth E. (author)
University of Copenhagen
Nielsen, Morten A. (author)
University of Copenhagen
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 (creator_code:org_t)
2016-05-26
2016
English 12 s.
In: Malaria Journal. - : Springer Science and Business Media LLC. - 1475-2875. ; 15:1, s. 1-12
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: Placental malaria occurs when Plasmodium falciparum infected erythrocytes sequester in the placenta. Placental parasite isolates bind to chondroitin sulphate A (CSA) by expression of VAR2CSA on the surface of infected erythrocytes, but may sequester by other VAR2CSA mediated mechanisms, such as binding to immunoglobulins. Furthermore, other parasite antigens have been associated with placental malaria. These findings have important implications for placental malaria vaccine design. The objective of this study was to adapt and describe a biologically relevant model of parasite adhesion in intact placental tissue. Results: The ex vivo placental perfusion model was modified to study adhesion of infected erythrocytes binding to CSA, endothelial protein C receptor (EPCR) or a transgenic parasite where P. falciparum erythrocyte membrane protein 1 expression had been shut down. Infected erythrocytes expressing VAR2CSA accumulated in perfused placental tissue whereas the EPCR binding and the transgenic parasite did not. Soluble CSA and antibodies specific against VAR2CSA inhibited binding of infected erythrocytes. Conclusion: The ex vivo model provides a novel way of studying receptor-ligand interactions and antibody mediated inhibition of binding in placental malaria.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Infektionsmedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Infectious Medicine (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Reproduktionsmedicin och gynekologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Obstetrics, Gynaecology and Reproductive Medicine (hsv//eng)

Keyword

Placental malaria
Placental perfusion
VAR2CSA

Publication and Content Type

art (subject category)
ref (subject category)

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