ICAM-1 Kilifi variant is not associated with cerebral and severe malaria pathogenesis in Beninese children
Cytoadhesion and sequestration of Plasmodium falciparum infected red blood cells (iRBC) in the microvasculature of vital organs are a major cause of malaria pathology. Several studies have provided evidence on the implication of the human host intercellular adhesion molecule-1 (ICAM-1) as a major re...
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Published in | Malaria journal Vol. 21; no. 1; p. 115 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
BioMed Central Ltd
04.04.2022
BioMed Central BMC |
Subjects | |
Online Access | Get full text |
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Summary: | Cytoadhesion and sequestration of Plasmodium falciparum infected red blood cells (iRBC) in the microvasculature of vital organs are a major cause of malaria pathology. Several studies have provided evidence on the implication of the human host intercellular adhesion molecule-1 (ICAM-1) as a major receptor for iRBCs binding to P. falciparum erythrocyte membrane protein 1 (PfEMP1) in the development of severe and cerebral malaria. The genetic polymorphism K29M in the immunoglobulin-like domain of ICAM-1, known as ICAM-1
, has been associated with either increased or decreased risk of developing cerebral malaria.
To provide more conclusive results, the genetic polymorphism of ICAM-1
was assessed by PCR and sequencing in blood samples from 215 Beninese children who presented with either mild or severe malaria including cerebral malaria.
The results showed that in this cohort of Beninese children, the ICAM-1
variant is present at the frequencies of 0.27, similar to the frequency observed in other African countries. This ICAM-1
variant was not associated with disease severity in agreement with other findings from the Gambia, Tanzania, Malawi, Gabon, and Thailand, suggesting no evidence of a direct link between this polymorphism and the pathogenesis of severe and cerebral malaria. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 PMCID: PMC8978164 |
ISSN: | 1475-2875 1475-2875 |
DOI: | 10.1186/s12936-022-04139-0 |