Association of cytokine and Toll-like receptor gene polymorphisms with severe malaria in three regions of Cameroon

P. falciparum malaria is one of the most widespread and deadliest infectious diseases in children under five years in endemic areas. The disease has been a strong force for evolutionary selection in the human genome, and uncovering the critical human genetic factors that confer resistance to the dis...

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Main Authors: Apinjoh, T, Anchang-Kimbi, J, Njua-Yafi, C, Mugri, R, Ngwai, A, Rockett, K, Mbunwe, E, Besingi, R, Clark, T, Kwiatkowski, D, Achidi, E
格式: Journal article
語言:English
出版: Public Library of Science 2013
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author Apinjoh, T
Anchang-Kimbi, J
Njua-Yafi, C
Mugri, R
Ngwai, A
Rockett, K
Mbunwe, E
Besingi, R
Clark, T
Kwiatkowski, D
Achidi, E
author_facet Apinjoh, T
Anchang-Kimbi, J
Njua-Yafi, C
Mugri, R
Ngwai, A
Rockett, K
Mbunwe, E
Besingi, R
Clark, T
Kwiatkowski, D
Achidi, E
author_sort Apinjoh, T
collection OXFORD
description P. falciparum malaria is one of the most widespread and deadliest infectious diseases in children under five years in endemic areas. The disease has been a strong force for evolutionary selection in the human genome, and uncovering the critical human genetic factors that confer resistance to the disease would provide clues to the molecular basis of protective immunity that would be invaluable for vaccine development. We investigated the effect of single nucleotide polymorphisms (SNPs) on malaria pathology in a case- control study of 1862 individuals from two major ethnic groups in three regions with intense perennial P. falciparum transmission in Cameroon. Twenty nine polymorphisms in cytokine and toll-like receptor (TLR) genes as well as the sickle cell trait (HbS) were assayed on the Sequenom iPLEX platform. Our results confirm the known protective effect of HbS against severe malaria and also reveal a protective effect of SNPs in interleukin-10 (IL10) cerebral malaria and hyperpyrexia. Furthermore, IL17RE rs708567 GA and hHbS rs334 AT individuals were associated with protection from uncomplicated malaria and anaemia respectively in this study. Meanwhile, individuals with the hHbS rs334 TT, IL10 rs3024500 AA, and IL17RD rs6780995 GA genotypes were more susceptible to severe malarial anaemia, cerebral malaria, and hyperpyrexia respectively. Taken together, our results suggest that polymorphisms in some immune response genes may have important implications for the susceptibility to severe malaria in Cameroonians. Moreover using uncomplicated malaria may allow us to identify novel pathways in the early development of the disease.
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spelling oxford-uuid:725b417f-2bb9-4d5a-8cb2-3b51f4306de82022-03-26T19:49:39ZAssociation of cytokine and Toll-like receptor gene polymorphisms with severe malaria in three regions of CameroonJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:725b417f-2bb9-4d5a-8cb2-3b51f4306de8EnglishSymplectic Elements at OxfordPublic Library of Science2013Apinjoh, TAnchang-Kimbi, JNjua-Yafi, CMugri, RNgwai, ARockett, KMbunwe, EBesingi, RClark, TKwiatkowski, DAchidi, EP. falciparum malaria is one of the most widespread and deadliest infectious diseases in children under five years in endemic areas. The disease has been a strong force for evolutionary selection in the human genome, and uncovering the critical human genetic factors that confer resistance to the disease would provide clues to the molecular basis of protective immunity that would be invaluable for vaccine development. We investigated the effect of single nucleotide polymorphisms (SNPs) on malaria pathology in a case- control study of 1862 individuals from two major ethnic groups in three regions with intense perennial P. falciparum transmission in Cameroon. Twenty nine polymorphisms in cytokine and toll-like receptor (TLR) genes as well as the sickle cell trait (HbS) were assayed on the Sequenom iPLEX platform. Our results confirm the known protective effect of HbS against severe malaria and also reveal a protective effect of SNPs in interleukin-10 (IL10) cerebral malaria and hyperpyrexia. Furthermore, IL17RE rs708567 GA and hHbS rs334 AT individuals were associated with protection from uncomplicated malaria and anaemia respectively in this study. Meanwhile, individuals with the hHbS rs334 TT, IL10 rs3024500 AA, and IL17RD rs6780995 GA genotypes were more susceptible to severe malarial anaemia, cerebral malaria, and hyperpyrexia respectively. Taken together, our results suggest that polymorphisms in some immune response genes may have important implications for the susceptibility to severe malaria in Cameroonians. Moreover using uncomplicated malaria may allow us to identify novel pathways in the early development of the disease.
spellingShingle Apinjoh, T
Anchang-Kimbi, J
Njua-Yafi, C
Mugri, R
Ngwai, A
Rockett, K
Mbunwe, E
Besingi, R
Clark, T
Kwiatkowski, D
Achidi, E
Association of cytokine and Toll-like receptor gene polymorphisms with severe malaria in three regions of Cameroon
title Association of cytokine and Toll-like receptor gene polymorphisms with severe malaria in three regions of Cameroon
title_full Association of cytokine and Toll-like receptor gene polymorphisms with severe malaria in three regions of Cameroon
title_fullStr Association of cytokine and Toll-like receptor gene polymorphisms with severe malaria in three regions of Cameroon
title_full_unstemmed Association of cytokine and Toll-like receptor gene polymorphisms with severe malaria in three regions of Cameroon
title_short Association of cytokine and Toll-like receptor gene polymorphisms with severe malaria in three regions of Cameroon
title_sort association of cytokine and toll like receptor gene polymorphisms with severe malaria in three regions of cameroon
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