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Acquisition of IgG to ICAM-1-Binding DBLβ Domains in the Plasmodium falciparum Erythrocyte Membrane Protein 1 Antigen Family Varies between Groups A, B, and C

Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) is an important malaria virulence factor. The protein family can be divided into clinically relevant subfamilies. ICAM-1-binding group A PfEMP1 proteins also bind endothelial protein C receptor and have been associated with cerebral malar...

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Autores principales: Olsen, Rebecca W., Ecklu-Mensah, Gertrude, Bengtsson, Anja, Ofori, Michael F., Kusi, Kwadwo A., Koram, Kwadwo A., Hviid, Lars, Adams, Yvonne, Jensen, Anja T. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759304/
https://www.ncbi.nlm.nih.gov/pubmed/31308082
http://dx.doi.org/10.1128/IAI.00224-19
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author Olsen, Rebecca W.
Ecklu-Mensah, Gertrude
Bengtsson, Anja
Ofori, Michael F.
Kusi, Kwadwo A.
Koram, Kwadwo A.
Hviid, Lars
Adams, Yvonne
Jensen, Anja T. R.
author_facet Olsen, Rebecca W.
Ecklu-Mensah, Gertrude
Bengtsson, Anja
Ofori, Michael F.
Kusi, Kwadwo A.
Koram, Kwadwo A.
Hviid, Lars
Adams, Yvonne
Jensen, Anja T. R.
author_sort Olsen, Rebecca W.
collection PubMed
description Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) is an important malaria virulence factor. The protein family can be divided into clinically relevant subfamilies. ICAM-1-binding group A PfEMP1 proteins also bind endothelial protein C receptor and have been associated with cerebral malaria in children. IgG to these PfEMP1 proteins is acquired later in life than that to group A PfEMP1 not binding ICAM-1. The kinetics of acquisition of IgG to group B and C PfEMP1 proteins binding ICAM-1 is unclear and was studied here. Gene sequences encoding group B and C PfEMP1 with DBLβ domains known to bind ICAM-1 were used to identify additional binders. Levels of IgG specific for DBLβ domains from group A, B, and C PfEMP1 binding or not binding ICAM-1 were measured in plasma from Ghanaian children with or without malaria. Seven new ICAM-1-binding DBLβ domains from group B and C PfEMP1 were identified. Healthy children had higher levels of IgG specific for ICAM-1-binding DBLβ domains from group A than from groups B and C. However, the opposite pattern was found in children with malaria, particularly among young patients. Acquisition of IgG specific for DBLβ domains binding ICAM-1 differs between PfEMP1 groups.
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spelling pubmed-67593042019-10-01 Acquisition of IgG to ICAM-1-Binding DBLβ Domains in the Plasmodium falciparum Erythrocyte Membrane Protein 1 Antigen Family Varies between Groups A, B, and C Olsen, Rebecca W. Ecklu-Mensah, Gertrude Bengtsson, Anja Ofori, Michael F. Kusi, Kwadwo A. Koram, Kwadwo A. Hviid, Lars Adams, Yvonne Jensen, Anja T. R. Infect Immun Cellular Microbiology: Pathogen-Host Cell Molecular Interactions Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) is an important malaria virulence factor. The protein family can be divided into clinically relevant subfamilies. ICAM-1-binding group A PfEMP1 proteins also bind endothelial protein C receptor and have been associated with cerebral malaria in children. IgG to these PfEMP1 proteins is acquired later in life than that to group A PfEMP1 not binding ICAM-1. The kinetics of acquisition of IgG to group B and C PfEMP1 proteins binding ICAM-1 is unclear and was studied here. Gene sequences encoding group B and C PfEMP1 with DBLβ domains known to bind ICAM-1 were used to identify additional binders. Levels of IgG specific for DBLβ domains from group A, B, and C PfEMP1 binding or not binding ICAM-1 were measured in plasma from Ghanaian children with or without malaria. Seven new ICAM-1-binding DBLβ domains from group B and C PfEMP1 were identified. Healthy children had higher levels of IgG specific for ICAM-1-binding DBLβ domains from group A than from groups B and C. However, the opposite pattern was found in children with malaria, particularly among young patients. Acquisition of IgG specific for DBLβ domains binding ICAM-1 differs between PfEMP1 groups. American Society for Microbiology 2019-09-19 /pmc/articles/PMC6759304/ /pubmed/31308082 http://dx.doi.org/10.1128/IAI.00224-19 Text en Copyright © 2019 Olsen et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Cellular Microbiology: Pathogen-Host Cell Molecular Interactions
Olsen, Rebecca W.
Ecklu-Mensah, Gertrude
Bengtsson, Anja
Ofori, Michael F.
Kusi, Kwadwo A.
Koram, Kwadwo A.
Hviid, Lars
Adams, Yvonne
Jensen, Anja T. R.
Acquisition of IgG to ICAM-1-Binding DBLβ Domains in the Plasmodium falciparum Erythrocyte Membrane Protein 1 Antigen Family Varies between Groups A, B, and C
title Acquisition of IgG to ICAM-1-Binding DBLβ Domains in the Plasmodium falciparum Erythrocyte Membrane Protein 1 Antigen Family Varies between Groups A, B, and C
title_full Acquisition of IgG to ICAM-1-Binding DBLβ Domains in the Plasmodium falciparum Erythrocyte Membrane Protein 1 Antigen Family Varies between Groups A, B, and C
title_fullStr Acquisition of IgG to ICAM-1-Binding DBLβ Domains in the Plasmodium falciparum Erythrocyte Membrane Protein 1 Antigen Family Varies between Groups A, B, and C
title_full_unstemmed Acquisition of IgG to ICAM-1-Binding DBLβ Domains in the Plasmodium falciparum Erythrocyte Membrane Protein 1 Antigen Family Varies between Groups A, B, and C
title_short Acquisition of IgG to ICAM-1-Binding DBLβ Domains in the Plasmodium falciparum Erythrocyte Membrane Protein 1 Antigen Family Varies between Groups A, B, and C
title_sort acquisition of igg to icam-1-binding dblβ domains in the plasmodium falciparum erythrocyte membrane protein 1 antigen family varies between groups a, b, and c
topic Cellular Microbiology: Pathogen-Host Cell Molecular Interactions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759304/
https://www.ncbi.nlm.nih.gov/pubmed/31308082
http://dx.doi.org/10.1128/IAI.00224-19
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